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        <title>Chromosoma via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Chromosoma' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Chromosoma&t=Chromosoma&s=Search&f=source]]></link>
        <lastBuildDate>Fri, 19 Mar 2010 17:00:25 +0100</lastBuildDate>
        <item>
            <title>Cyclin G-associated kinase promotes microtubule outgrowth from chromosomes during spindle assembly</title>
            <link>http://www.medworm.com/index.php?rid=3377274&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fvmg2736228237r33%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;During mitosis, all chromosomes must attach to microtubules of the mitotic spindle to ensure correct chromosome segregation.
 Microtubule attachment occurs at specialized structures at the centromeric region of chromosomes, called kinetochores. These
 kinetochores can generate microtubule attachments through capture of centrosome-derived microtubules, but in addition, they
 can generate microtubules themselves, which are subsequently integrated with centrosome-derived microtubules to form the mitotic
 spindle. Here, we have performed a large scale RNAi screen and identify cyclin G-associated kinase (GAK) as a novel regulator
 of microtubule generation at kinetochores/chromatin. This function of GAK requires its C-terminal J-domain, which is essential
 for clathrin recyc...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3377274</comments>
            <pubDate>Tue, 16 Mar 2010 14:49:18 +0100</pubDate>
            <guid isPermaLink="false">3377274</guid>        </item>
        <item>
            <title>Positional variations among heterogeneous nucleosome maps give dynamical information on chromatin</title>
            <link>http://www.medworm.com/index.php?rid=3361722&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2027175265xw3212%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Although nucleosome remodeling is essential to transcriptional regulation in eukaryotes, little is known about its genome-wide
 behavior. Since a number of nucleosome positioning maps in vivo have been recently determined, we examined if their comparisons
 might be used for obtaining a genome-wide profile of nucleosome remodeling. Using seven yeast maps, the local variability
 of nucleosomes, measured by the entropy, was significantly higher in a set of reported unstable nucleosomes. The binding sites
 of four transcription factors, known as the remodeling factors, were distinctively high both in entropy and linker ratio,
 whereas those of Yhp1, their potential inhibitor, showed the lowest values in both of them. Taken together, our map shows
 the general information of...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3361722</comments>
            <pubDate>Thu, 11 Mar 2010 18:12:23 +0100</pubDate>
            <guid isPermaLink="false">3361722</guid>        </item>
        <item>
            <title>MDC1: The art of keeping things in focus</title>
            <link>http://www.medworm.com/index.php?rid=3361721&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa5401p23382128l8%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The chromatin structure is important for recognition and repair of DNA damage. Many DNA damage response proteins accumulate
 in large chromatin domains flanking sites of DNA double-strand breaks. The assembly of these structures—usually termed DNA
 damage foci—is primarily regulated by MDC1, a large nuclear mediator/adaptor protein that is composed of several distinct
 structural and functional domains. Here, we are summarizing the latest discoveries about the mechanisms by which MDC1 mediates
 DNA damage foci formation, and we are reviewing the considerable efforts taken to understand the functional implication of
 these structures.
 
 
	Content Type Journal ArticleCategory REVIEWDOI 10.1007/s00412-010-0266-9Authors
		Stephanie Jungmichel, University of Zürich Ins...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3361721</comments>
            <pubDate>Thu, 11 Mar 2010 18:12:23 +0100</pubDate>
            <guid isPermaLink="false">3361721</guid>        </item>
        <item>
            <title>Heterochromatin and histone modifications in the germline-restricted chromosome of the zebra finch undergoing elimination during spermatogenesis</title>
            <link>http://www.medworm.com/index.php?rid=3357684&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb2226p287h1u3649%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In the zebra finch (Taeniopygia guttata) a germline-restricted chromosome (GRC) is regularly present in males and females. While the GRC is euchromatic in oocytes,
 in spermatocytes this chromosome is cytologically seen as entirely heterochromatic and presumably inactive. At the end of
 male meiosis, the GRC is eliminated from the nucleus. By immunofluorescence on microspreads, we investigated HP1 proteins
 and histone modifications throughout male meiotic prophase, as well as in young spermatid stages after the GRC elimination.
 We found that in prophase spermatocytes the GRC chromatin differs from that of the regular chromosome complement. The GRC
 is highly enriched in HP1β and exhibits high levels of di- and tri-methylated histone H3 at lysine 9 and tri- and di-met...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3357684</comments>
            <pubDate>Wed, 10 Mar 2010 16:14:36 +0100</pubDate>
            <guid isPermaLink="false">3357684</guid>        </item>
        <item>
            <title>Development and analysis of a germline BAC resource for the sea lamprey, a vertebrate that undergoes substantial chromatin diminution</title>
            <link>http://www.medworm.com/index.php?rid=3325897&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl33784853329h121%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Over the last several years, the sea lamprey (Petromyzon marinus) has grown substantially as a model for understanding the evolutionary fundaments and capacity of vertebrate developmental
 and genome biology. Recent work on the lamprey genome has resulted in a preliminary assembly of the lamprey genome and led
 to the realization that nearly all somatic cell lineages undergo extensive programmed rearrangements. Here we describe the
 development of a bacterial artificial chromosome (BAC) resource for lamprey germline DNA and use sequence information from
 this resource to probe the subchromosomal structure of the lamprey genome. The arrayed germline BAC library represents ∼10×
 coverage of the lamprey genome. Analyses of BAC-end sequences reveal that the lamprey genom...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3325897</comments>
            <pubDate>Mon, 01 Mar 2010 18:07:55 +0100</pubDate>
            <guid isPermaLink="false">3325897</guid>        </item>
        <item>
            <title>CTCF shapes chromatin by multiple mechanisms: the impact of 20 years of CTCF research on understanding the workings of chromatin</title>
            <link>http://www.medworm.com/index.php?rid=3297494&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ffh784k0828h732j7%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;More than 109 base pairs of the genome in higher eucaryotes are positioned in the interphase nucleus such that gene activation, gene repression,
 remote gene regulation by enhancer elements, and reading as well as adjusting epigenetic marks are possible. One important
 structural and functional component of chromatin organization is the zinc finger factor CTCF. Two decades of research has
 advanced the understanding of the fundamental role that CTCF plays in regulating such a vast expanse of DNA.
 
 
	Content Type Journal ArticleCategory REVIEWDOI 10.1007/s00412-010-0262-0Authors
		Rolf Ohlsson, Karolinska Institute Institute for Microbiology, Tumor- and Cellbiology (MTC) Stockholm SwedenMarek Bartkuhn, Justus-Liebig-University Institute for Genetics 35392 Giessen Germa...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3297494</comments>
            <pubDate>Sat, 20 Feb 2010 06:50:17 +0100</pubDate>
            <guid isPermaLink="false">3297494</guid>        </item>
        <item>
            <title>Meiotic silencing and fragmentation of the male germline restricted chromosome in zebra finch</title>
            <link>http://www.medworm.com/index.php?rid=3282717&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe11532x5101k5301%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;During male meiotic prophase in mammals, X and Y are in a largely unsynapsed configuration, which is thought to trigger meiotic
 sex chromosome inactivation (MSCI). In avian species, females are ZW, and males ZZ. Although Z and W in chicken oocytes show
 complete, largely heterologous synapsis, they too undergo MSCI, albeit only transiently. The W chromosome is already inactive
 in early meiotic prophase, and inactive chromatin marks may spread on to the Z upon synapsis. Mammalian MSCI is considered
 as a specialised form of the general meiotic silencing mechanism, named meiotic silencing of unsynapsed chromatin (MSUC).
 Herein, we studied the avian form of MSUC, by analysing the behaviour of the peculiar germline restricted chromosome (GRC)
 that is present as a single...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3282717</comments>
            <pubDate>Tue, 16 Feb 2010 18:06:04 +0100</pubDate>
            <guid isPermaLink="false">3282717</guid>        </item>
        <item>
            <title>Re-evaluating the role of Tao1 in the spindle checkpoint</title>
            <link>http://www.medworm.com/index.php?rid=3282718&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5230476172434271%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The spindle checkpoint restrains anaphase onset and mitotic exit until all chromosomes are stably attached to the mitotic
 spindle via their kinetochores. The Tao1 protein kinase was recently reported as a novel spindle checkpoint component. When
 an siRNA was used to repress Tao1, the essential spindle checkpoint component Mad2 failed to localise to kinetochores, and
 cells rapidly exited mitosis. Tao1 was also shown to interact with BubR1, another essential checkpoint component, and be rapidly
 degraded after mitosis, a feature typical of many mitotic regulators. Here, we identify four different siRNAs that repress
 Tao1 protein levels as efficiently as the previously reported siRNA. However, these siRNAs do not override the spindle checkpoint.
 We also present data i...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3282718</comments>
            <pubDate>Tue, 16 Feb 2010 18:06:00 +0100</pubDate>
            <guid isPermaLink="false">3282718</guid>        </item>
        <item>
            <title>Minichromosome stability induced by partial genome duplication in Arabidopsis thaliana</title>
            <link>http://www.medworm.com/index.php?rid=3270859&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ffh0hr11587231u62%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Two partially reconstructed karyotypes (RK1 and RK2) of Arabidopsis thaliana have been established from a transformant, in which four structurally changed chromosomes (α, β, γ, and δ) were involved. Both karyotypes are composed of 12 chromosomes, 

 2n = 1¢¢+ 3¢¢+ 4¢¢+ 5¢¢+ a¢¢+ g¢¢ = 12 
 for RK1 and 

 2n = 3¢¢+ 4¢¢+ 5¢¢+ a¢¢+ b¢¢+ g¢¢ = 12 
 for RK2, and these chromosome constitutions were relatively stable at least for three generations. Pairing at meiosis was
 limited to the homologues (1, 3, 4, 5, α, β, or γ), and no pairing occurred among non-homologous chromosomes in both karyotypes. For minichromosome α (mini α), precocious separation at metaphase I was frequently observed in RK2, as found for other minichromosomes, but was rare...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3270859</comments>
            <pubDate>Fri, 12 Feb 2010 07:08:13 +0100</pubDate>
            <guid isPermaLink="false">3270859</guid>        </item>
        <item>
            <title>Drosophila D1 overexpression induces ectopic pairing of polytene chromosomes and is deleterious to development</title>
            <link>http://www.medworm.com/index.php?rid=3242721&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6177u43k8ju14384%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Eukaryotic genomes function in the context of chromatin, but the roles of most nonhistone chromosomal proteins are far from
 understood. The D1 protein of Drosophila is an example of a chromosomal protein that has been fairly well characterized biochemically, but has nevertheless eluded
 functional description. To this end, we have undertaken a gain-of-function genetical analysis of D1, utilizing the GAL4-UAS system. We determined that ubiquitous overexpression of D1 using the Act5C- or tubP-GAL4 drivers was lethal to the organism during larval growth. We also ectopically expressed D1 in a tissue-limited manner using other GAL4 drivers. In general, ectopic D1 was observed to inhibit differentiation and/or development. We observed effects on pattern
 formation of the adu...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3242721</comments>
            <pubDate>Tue, 02 Feb 2010 17:47:25 +0100</pubDate>
            <guid isPermaLink="false">3242721</guid>        </item>
        <item>
            <title>Structure and size variations between 12A and 12D homoeologous chromosomes based on high-resolution cytogenetic map in allotetraploid cotton</title>
            <link>http://www.medworm.com/index.php?rid=3234639&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv6k43684v660844q%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cotton is a model system for studying polyploidization, genomic organization, and genome-size variation because the allotetraploid
 was formed 1-2&amp;nbsp;million years ago, which is old enough for sequence divergence but relatively recent to maintain genome stability.
 In spite of characterizing random genomic sequences in many polyploidy plants, the cytogenetic and sequence data that decipher
 homoeologous chromosomes are very limited in allopolyploid species. Here, we reported comprehensive analyses of integrated
 cytogenetic and linkage maps of homoeologous chromosomes 12A and 12D in allotetraploid cotton using fluorescence in situ hybridization
 and a large number of bacterial artificial chromosomes that were anchored by simple sequence repeat markers in the correspon...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3234639</comments>
            <pubDate>Mon, 01 Feb 2010 18:02:39 +0100</pubDate>
            <guid isPermaLink="false">3234639</guid>        </item>
        <item>
            <title>Mechanism of haploidy-dependent unreductional meiotic cell division in polyploid wheat</title>
            <link>http://www.medworm.com/index.php?rid=3234640&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4rr027r13010j5p1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Unreductional meiotic cell division (UMCD) generates unreduced gametes and leads to polyploidy. The tetraploid wheat “Langdon”
 (LDN) undergoes normal meiosis, but its polyhaploid undergoes UMCD. Here, we found that sister kinetochores oriented syntelically
 at meiosis I in LDN, but amphitelically in LDN polyhaploid and the interspecific hybrid of LDN with Aegilops tauschii. We also observed that sister centromere cohesion persisted until anaphase II in LDN, LDN polyhaploid, and the interspecific
 hybrid. Meiocytes with all chromosomes oriented amphitelically underwent UMCD in LDN polyhaploid, and the interspecific hybrid,
 suggesting the tension created by the amphitelic orientation of sister kinetochores and persistence of centromeric cohesion
 between sister chro...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3234640</comments>
            <pubDate>Mon, 01 Feb 2010 18:02:37 +0100</pubDate>
            <guid isPermaLink="false">3234640</guid>        </item>
        <item>
            <title>Calpain 2 is required for sister chromatid cohesion</title>
            <link>http://www.medworm.com/index.php?rid=3207491&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe52604v313vr74w5%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Calpains form a family of Ca2+-dependent cysteine proteases involved in diverse cellular processes. However, the specific functions of each calpain isoform
 remain unknown. Recent reports have shown that calpain 2 (Capn2) is essential for cell viability. We have recently shown that
 Capn2 is a nuclear protease associated with chromosomes during mitosis in mammalian embryonic cells. We now report that Capn2
 depletion impairs mitosis and induces apoptosis in murine cells. Low Capn2 levels induce chromosome alignment defects, the
 loss of histone H3 threonine 3 phosphorylation at centromeres, and premature sister chromatid separation. Thus, Capn2 may
 play a role in fundamental mitotic functions, such as the maintenance of sister chromatid cohesion.
 
	Content Type Journa...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3207491</comments>
            <pubDate>Fri, 22 Jan 2010 10:08:52 +0100</pubDate>
            <guid isPermaLink="false">3207491</guid>        </item>
        <item>
            <title>E(y)2/Sus1 is required for blocking PRE silencing by the Wari insulator in Drosophila melanogaster</title>
            <link>http://www.medworm.com/index.php?rid=3192550&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj38668616n8207p7%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Chromatin insulators affect interactions between promoters and enhancers/silencers and function as barriers to the spread
 of repressive chromatin. Recently, we have found an insulator, named Wari, located on the 3′ side of the white gene. Here,
 we show that the previously identified 368-bp core of this insulator is sufficient for blocking Polycomb response element-mediated
 silencing. Although Wari does not contain binding sites for known insulator proteins, the E(y)2 and CP190 proteins bind to
 Wari as well as to the Su(Hw)-containing insulators in vivo. It may well be that these proteins are recruited to the insulator
 by as yet unidentified DNA-binding protein. Partial inactivation of E(y)2 in a weak e(y)2
 
 u1
 mutation impairs only the anti-silencing but not t...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3192550</comments>
            <pubDate>Fri, 15 Jan 2010 17:59:09 +0100</pubDate>
            <guid isPermaLink="false">3192550</guid>        </item>
        <item>
            <title>SUV39h-independent association of HP1β with fibrillarin-positive nucleolar regions</title>
            <link>http://www.medworm.com/index.php?rid=3121852&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F03353h53h300j70k%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Heterochromatin protein 1 (HP1), which binds to sites of histone H3 lysine 9 (H3K9) methylation, is primarily responsible
 for gene silencing and the formation of heterochromatin. We observed that HP1β is located in both the chromocenters and fibrillarin-positive
 nucleoli interiors. However, HP1α and HP1γ occupied fibrillarin-positive compartments to a lesser extent, corresponding to
 the distinct levels of HP1 subtypes at the promoter of rDNA genes. Deficiency of histone methyltransferases SUV39h and/or
 inhibition of histone deacetylases (HDACi) decreased HP1β and H3K9 trimethylation at chromocenters, but not in fibrillarin-positive
 regions that co-localized with RNA polymerase I. Similarly, SUV39h- and HDACi-dependent nucleolar rearrangement and inhibition
 of ...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3121852</comments>
            <pubDate>Wed, 23 Dec 2009 22:22:23 +0100</pubDate>
            <guid isPermaLink="false">3121852</guid>        </item>
        <item>
            <title>Chromatin insulators specifically associate with different levels of higher-order chromatin organization in Drosophila</title>
            <link>http://www.medworm.com/index.php?rid=3121853&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fpg52448206047278%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Chromatin insulators are required for proper temporal and spatial expression of genes in metazoans. Here, we have analyzed
 the distribution of insulator proteins on the 56F–58A region of chromosome 2R in Drosophila polytene chromosomes to assess the role of chromatin insulators in shaping genome architecture. Data show that the suppressor
 of Hairy-wing protein [Su(Hw)] is found in three structures differentially associated with insulator proteins: bands, interbands,
 and multi-gene domains of coexpressed genes. Results show that bands are generally formed by condensation of chromatin that
 belongs to genes containing one or more Su(Hw) binding sites, whereas, in interbands, Su(Hw) sites appear associated with
 open chromatin. In addition, clusters of coexpressed gen...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3121853</comments>
            <pubDate>Wed, 23 Dec 2009 22:22:21 +0100</pubDate>
            <guid isPermaLink="false">3121853</guid>        </item>
        <item>
            <title>B chromosome ancestry revealed by histone genes in the migratory locust</title>
            <link>http://www.medworm.com/index.php?rid=3106551&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F544q5163q5r273h5%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In addition to the standard set of chromosomes (A), about 15% of eukaryote genomes carry B chromosomes. In most cases, B chromosomes
 behave as genomic parasites being detrimental for the individuals carrying them and prospering in natural populations because
 of transmission advantages (drive). B chromosomes are mostly made up of repetitive DNA sequences, especially ribosomal DNA
 (rDNA), satellite DNA and mobile elements. In only two cases have B chromosomes been shown to carry protein-coding genes.
 Although some B chromosomes seem to have derived from interspecific hybridisation, the most likely source of B chromosomes
 is the host genome itself, but the specific A chromosome being the B ancestor has not been identified in any B-containing
 species. Here, we provide...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3106551</comments>
            <pubDate>Thu, 17 Dec 2009 07:03:37 +0100</pubDate>
            <guid isPermaLink="false">3106551</guid>        </item>
        <item>
            <title>Differential nuclear envelope assembly at the end of mitosis in suspension-cultured Apium graveolens cells</title>
            <link>http://www.medworm.com/index.php?rid=3081662&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9237h35814334452%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;NMCP1 is a plant protein that has a long coiled-coil domain within the molecule. Newly identified NMCP2 of Daucus carota and Apium graveolens showed similar peripheral localization in the interphase nucleus, and the sequence spanning the coiled-coil domain exhibited
 significant similarity with the corresponding region of NMCP1. To better understand disassembly and assembly of the nuclear
 envelope (NE) during mitosis, subcellular distribution of NMCP1 and NMCP2 was examined using A. graveolens cells. AgNMCP1 (NMCP1 in Apium) disassembled at prometaphase, dispersed mainly within the spindle, and accumulated on segregating chromosomes, while AgNMCP2
 (NMCP2 in Apium), following disassembly at prometaphase with timing similar to that of AgNMCP1, dispersed throughout the m...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3081662</comments>
            <pubDate>Tue, 08 Dec 2009 19:47:22 +0100</pubDate>
            <guid isPermaLink="false">3081662</guid>        </item>
        <item>
            <title>Haspin: a newly discovered regulator of mitotic chromosome behavior</title>
            <link>http://www.medworm.com/index.php?rid=3078163&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbr7163xw8q320125%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The haspins are divergent members of the eukaryotic protein kinase family that are conserved in many eukaryotic lineages including
 animals, fungi, and plants. Recently-solved crystal structures confirm that the kinase domain of human haspin has unusual
 structural features that stabilize a catalytically active conformation and create a distinctive substrate binding site. Haspin
 localizes predominantly to chromosomes and phosphorylates histone H3 at threonine-3 during mitosis, particularly at inner
 centromeres. This suggests that haspin directly regulates chromosome behavior by modifying histones, although it is likely
 that additional substrates will be identified in the future. Depletion of haspin by RNA interference in human cell lines causes
 premature loss of cen...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3078163</comments>
            <pubDate>Tue, 08 Dec 2009 06:45:21 +0100</pubDate>
            <guid isPermaLink="false">3078163</guid>        </item>
        <item>
            <title>Coilin phosphorylation mediates interaction with SMN and SmB′</title>
            <link>http://www.medworm.com/index.php?rid=3078164&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4776p64k6p3k62u0%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cajal bodies (CBs) are subnuclear domains that participate in spliceosomal small nuclear ribonucleoprotein (snRNP) biogenesis
 and play a part in the assembly of the spliceosomal complex. The CB marker protein, coilin, interacts with survival of motor
 neuron (SMN) and Sm proteins. Several coilin phosphoresidues have been identified by mass spectrometric analysis. Phosphorylation
 of coilin affects its self-interaction and localization in the nucleus. We hypothesize that coilin phosphorylation also impacts
 its binding to SMN and Sm proteins. In vitro binding studies with a C-terminal fragment of coilin and corresponding phosphomimics
 show that SMN binds preferentially to dephosphorylated analogs and that SmB′ binds preferentially to phosphomimetic constructs.
 Bacte...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3078164</comments>
            <pubDate>Mon, 07 Dec 2009 19:35:24 +0100</pubDate>
            <guid isPermaLink="false">3078164</guid>        </item>
        <item>
            <title>Widespread regulation of gene expression in the Drosophila genome by the histone acetyltransferase dTip60</title>
            <link>http://www.medworm.com/index.php?rid=3055408&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6h60564544758766%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The MYST histone acetyltransferase (HAT) dTip60 is part of a multimeric protein complex that unites both HAT and chromatin
 remodeling activities. Here, we sought to gain insight into the biological functions of dTip60. Strong ubiquitous dTip60 knock-down
 in flies was lethal, whereas knock-down in the wing imaginal disk led to developmental defects in the wing. dTip60 localized
 to the nucleus in early embryos and was present in a large number of interbands on polytene chromosomes. Genome-wide expression
 analysis upon depletion of dTip60 in cell culture showed that it regulated a large number of genes in Drosophila, among which those with chromatin-related functions were highly enriched. Surprisingly, a significant portion of these genes
 were upregulated upon dTip60 ...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3055408</comments>
            <pubDate>Tue, 01 Dec 2009 08:30:00 +0100</pubDate>
            <guid isPermaLink="false">3055408</guid>        </item>
        <item>
            <title>Chromosomal and telomeric reprogramming following ES-somatic cell fusion</title>
            <link>http://www.medworm.com/index.php?rid=2987910&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv9821150lk023723%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Chromosomal and telomeric reprogramming was assessed in intraspecies hybrids obtained by fusion of embryonic stem (ES) cells
 and mouse embryonic fibroblasts. Evaluation of the ploidy of ES-somatic hybrids revealed that 21 of 59 clones had a tetraploid
 DNA profile while the remaining clones showed deviations from the expected profile of fusion between two diploid cells. Microsatellite
 polymerase chain reaction analysis of four of these clones demonstrated no random loss of somatic chromosome pairs in the
 ES-somatic cell hybrids. Pluripotential of ES-somatic hybrids was assessed by gene expression analysis, antibody staining
 for Oct4 and SSEA-1 and teratoma formation containing derivatives of the three germ layers. Reprogramming of telomeric maintenance
 was observed...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2987910</comments>
            <pubDate>Wed, 11 Nov 2009 07:05:39 +0100</pubDate>
            <guid isPermaLink="false">2987910</guid>        </item>
        <item>
            <title>Re-examination of siRNA specificity questions role of PICH and Tao1 in the spindle checkpoint and identifies Mad2 as a sensitive target for small RNAs</title>
            <link>http://www.medworm.com/index.php?rid=2987911&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F292xl556r480671m%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The DNA-dependent adenosine triphosphatase (ATPase) Plk1-interacting checkpoint helicase (PICH) has recently been implicated
 in spindle checkpoint (SAC) signaling (Baumann et al., Cell 128(1):101–114, 2007). Depletion of PICH by siRNA abolished the SAC and resulted in an apparently selective loss of Mad2 from kinetochores, suggesting
 a role for PICH in the regulation of the Mad1–Mad2 interaction. An apparent rescue of SAC functionality by overexpression
 of PICH in PICH-depleted cells initially seemed to confirm a role for PICH in the SAC. However, we have subsequently discovered
 that all PICH-directed siRNA oligonucleotides that abolish the SAC also reduce Mad2 mRNA and protein expression. This reduction
 is functionally significant, as PICH siRNA does not aboli...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2987911</comments>
            <pubDate>Tue, 10 Nov 2009 18:45:07 +0100</pubDate>
            <guid isPermaLink="false">2987911</guid>        </item>
        <item>
            <title>MRN and the race to the break</title>
            <link>http://www.medworm.com/index.php?rid=2937818&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fdh2jqp2t2886r2p3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In all living cells, DNA is constantly threatened by both endogenous and exogenous agents. In order to protect genetic information,
 all cells have developed a sophisticated network of proteins, which constantly monitor genomic integrity. This network, termed
 the DNA damage response, senses and signals the presence of DNA damage to effect numerous biological responses, including
 DNA repair, transient cell cycle arrests (“checkpoints”) and apoptosis. The MRN complex (MRX in yeast), composed of Mre11,
 Rad50 and Nbs1 (Xrs2), is a key component of the immediate early response to DNA damage, involved in a cross-talk between
 the repair and checkpoint machinery. Using its ability to bind DNA ends, it is ideally placed to sense and signal the presence
 of double strand ...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2937818</comments>
            <pubDate>Tue, 27 Oct 2009 17:59:31 +0100</pubDate>
            <guid isPermaLink="false">2937818</guid>        </item>
        <item>
            <title>Synaptonemal complex stability depends on repressive histone marks of the lateral element-associated repeat sequences</title>
            <link>http://www.medworm.com/index.php?rid=2881042&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3247744j7403937x%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The synaptonemal complex (SC) is the central key structure for meiosis in organisms undergoing sexual reproduction. During
 meiotic prophase I, homologous chromosomes exchange genetic information at the time they are attached to the lateral elements
 by specific DNA sequences. Most of these sequences, so far identified, consist of repeat DNA, which are subject to chromatin
 structural changes during meiotic prophase I. In this work, we addressed the effect of altering the chromatin structure of
 repeat DNA sequences mediating anchorage to the lateral elements of the SC. Administration of the histone deacetylase inhibitor
 trichostatin A into live rats caused death of cells in the pachytene stage as well as changes in histone marks along the synaptonemal
 complex. The mo...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2881042</comments>
            <pubDate>Fri, 09 Oct 2009 06:06:50 +0100</pubDate>
            <guid isPermaLink="false">2881042</guid>        </item>
        <item>
            <title>SUMOylation is required for normal development of linear elements and wild-type meiotic recombination in Schizosaccharomyces pombe</title>
            <link>http://www.medworm.com/index.php?rid=2812009&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fal81823nq251v365%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In the fission yeast, Schizosaccharomyces pombe, synaptonemal complexes (SCs) are not formed during meiotic prophase. However, structures resembling the axial elements of
 SCs, the so-called linear elements (LinEs) appear. By in situ immunostaining, we found Pmt3 (S. pombe's SUMO protein) transiently along LinEs, suggesting that SUMOylation of some component(s) of LinEs occurs during meiosis.
 Mutation of the SUMO ligase Pli1 caused aberrant LinE formation and reduced genetic recombination indicating a role for SUMOylation
 of LinEs for the regulation of meiotic recombination. Western blot analysis of TAP-tagged Rec10 demonstrated that there is
 a Pli1-dependent posttranslational modification of this protein, which is a major LinE component and a distant homolog of
 the...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2812009</comments>
            <pubDate>Wed, 16 Sep 2009 18:49:44 +0100</pubDate>
            <guid isPermaLink="false">2812009</guid>        </item>
        <item>
            <title>Divergence in centromere structure distinguishes related genomes in Coix lacryma-jobi and its wild relative</title>
            <link>http://www.medworm.com/index.php?rid=2812008&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa202pn7t3203206k%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Knowledge about the composition and structure of centromeres is critical for understanding how centromeres perform their functional
 roles. Here, we report the sequences of one centromere-associated bacterial artificial chromosome clone from a Coix lacryma-jobi library. Two Ty3/gypsy-class retrotransposons, centromeric retrotransposon of C. lacryma-jobi (CRC) and peri-centromeric retrotransposon of C. lacryma-jobi, and a (peri)centromere-specific tandem repeat with a unit length of 153&amp;nbsp;bp were identified. The CRC is highly homologous to centromere-specific retrotransposons reported in grass species. An 80-bp DNA region in the 153-bp
 satellite repeat was found to be conserved to centromeric satellite repeats from maize, rice, and pearl millet. Fluorescence
 in situ...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2812008</comments>
            <pubDate>Wed, 16 Sep 2009 18:49:44 +0100</pubDate>
            <guid isPermaLink="false">2812008</guid>        </item>
        <item>
            <title>Solving the Dnmt2 enigma</title>
            <link>http://www.medworm.com/index.php?rid=2812010&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr543qu673n481810%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Dnmt2 is a member of the animal DNA methyltransferase family of enzymes. While the role of other Dnmt proteins has been extensively
 characterized, comparably little is known about Dnmt2. This is surprising because Dnmt2 is the most widely conserved Dnmt
 protein, with homologues in protists, plants, fungi, and animals. In this review, we discuss the evidence supporting the seemingly
 contradictory roles of Dnmt2 in both DNA and RNA methylation. New studies are uncovering the enzymatic mechanisms that mediate
 these activities and also provide first insights into the biological functions of Dnmt2. Lastly, we also discuss observations
 that suggest a possible role for Dnmt2 in human health and disease, which further emphasizes the importance of defining Dnmt2-modulated
 ...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2812010</comments>
            <pubDate>Wed, 16 Sep 2009 18:49:42 +0100</pubDate>
            <guid isPermaLink="false">2812010</guid>        </item>
        <item>
            <title>Spatial organization of genes as a component of regulated expression</title>
            <link>http://www.medworm.com/index.php?rid=2768095&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9685562762225472%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The DNA of living cells is highly compacted. Inherent in this spatial constraint is the need for cells to organize individual
 genetic loci so as to facilitate orderly retrieval of information. Complex genetic regulatory mechanisms are crucial to all
 organisms, and it is becoming increasingly evident that spatial organization of genes is one very important mode of regulation
 for many groups of genes. In eukaryotic nuclei, it appears not only that DNA is organized in three-dimensional space but also
 that this organization is dynamic and interactive with the transcriptional state of the genes. Spatial organization occurs
 throughout evolution and with genes transcribed by all classes of RNA polymerases in all eukaryotic nuclei, from yeast to
 human. There is an increas...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2768095</comments>
            <pubDate>Thu, 03 Sep 2009 06:25:27 +0100</pubDate>
            <guid isPermaLink="false">2768095</guid>        </item>
        <item>
            <title>pRb, a local chromatin organizer with global possibilities</title>
            <link>http://www.medworm.com/index.php?rid=2745359&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3n4p23v47025p7n4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The retinoblastoma (pRb) family of proteins are well known for their tumor suppressor properties and for their ability to
 regulate transcription. The action of pRb family members correlates with the appearance of repressive chromatin marks at promoter
 regions of genes encoding key regulators of cell proliferation. Recent studies raise the possibility that pRb family members
 do not simply act by controlling the activity of individual promoters but that they may also function by promoting the more
 general organization of chromatin. In several contexts, pRb family members stimulate the compaction or condensation of chromatin
 and promote the formation of heterochromatin. In this review, we summarize studies that link pRb family members to the condensation
 or compactio...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2745359</comments>
            <pubDate>Fri, 28 Aug 2009 16:58:44 +0100</pubDate>
            <guid isPermaLink="false">2745359</guid>        </item>
        <item>
            <title>H2AX: functional roles and potential applications</title>
            <link>http://www.medworm.com/index.php?rid=2736853&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft02h80wv134g2507%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Upon DNA double-strand break (DSB) induction in mammals, the histone H2A variant, H2AX, becomes rapidly phosphorylated at
 serine 139. This modified form, termed γ-H2AX, is easily identified with antibodies and serves as a sensitive indicator of
 DNA DSB formation. This review focuses on the potential clinical applications of γ-H2AX detection in cancer and in response
 to other cellular stresses. In addition, the role of H2AX in homeostasis and disease will be discussed. Recent work indicates
 that γ-H2AX detection may become a powerful tool for monitoring genotoxic events associated with cancer development and tumor
 progression.
 
	Content Type Journal ArticleCategory Mini-ReviewDOI 10.1007/s00412-009-0234-4Authors
		Jennifer S. Dickey, National Institutes of Healt...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2736853</comments>
            <pubDate>Tue, 25 Aug 2009 16:45:57 +0100</pubDate>
            <guid isPermaLink="false">2736853</guid>        </item>
        <item>
            <title>Partitioning the C. elegans genome by nucleosome modification, occupancy, and positioning</title>
            <link>http://www.medworm.com/index.php?rid=2736854&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr0gw044155823242%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We have characterized two post-translational histone modifications in Caenorhabditis elegans on a genomic scale. Micrococcal nuclease digestion and immunoprecipitation were used to obtain distinct populations of single
 nucleosome cores, which were analyzed using massively parallel DNA sequencing to obtain positional and coverage maps. Two
 methylated histone H3 populations were chosen for comparison: H3K4 histone methylation (associated with active chromosomal
 regions) and H3K9 histone methylation (associated with inactivity). From analysis of the sequence data, we found nucleosome
 cores with these modifications to be enriched in two distinct partitions of the genome; H3K4 methylation was particularly
 prevalent in promoter regions of widely expressed genes, while H3...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2736854</comments>
            <pubDate>Tue, 25 Aug 2009 06:54:16 +0100</pubDate>
            <guid isPermaLink="false">2736854</guid>        </item>
        <item>
            <title>Histone3 variants in plants</title>
            <link>http://www.medworm.com/index.php?rid=2729138&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj46764538m277885%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Regulation of chromatin activity by covalent histone modifications has been long recognized. Histones that constitute the
 nucleosome are encoded by large families of genes and display a strong degree of conservation. However, histone variants exist
 and it is becoming clear that they play important roles in genome regulation. While most studies of the role of histone3 (H3)
 variants in transcriptional control comes from animal models, emerging data in plants suggest functional conservation, although
 plant-specific roles are likely. We review these data and speculate on the biological significance of H3 variants in plants.
 
	Content Type Journal ArticleCategory ReviewDOI 10.1007/s00412-009-0237-1Authors
		Mathieu Ingouff, National University of Singapore Department of...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2729138</comments>
            <pubDate>Sun, 23 Aug 2009 05:45:05 +0100</pubDate>
            <guid isPermaLink="false">2729138</guid>        </item>
        <item>
            <title>Macrosatellite epigenetics: the two faces of DXZ4 and D4Z4</title>
            <link>http://www.medworm.com/index.php?rid=2718756&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm01576p4205327jh%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Almost half of the human genome consists of repetitive DNA. Understanding what role these elements have in setting up chromatin
 states that underlie gene and chromosome function in complex genomes is paramount. The function of some types of repetitive
 DNA is obvious by virtue of their location, such as the alphoid arrays that define active centromeres. However, there are
 many other types of repetitive DNA whose evolutionary origins and current roles in genome biology remain unknown. One type
 of repetitive DNA that falls into this class is the macrosatellites. The relevance of these sequences to disease is clearly
 demonstrated by the 4q macrosatellite (D4Z4), whereupon contraction in the size of the array is associated with the onset
 of facioscapulohumeral muscular...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2718756</comments>
            <pubDate>Wed, 19 Aug 2009 08:29:23 +0100</pubDate>
            <guid isPermaLink="false">2718756</guid>        </item>
        <item>
            <title>Localization and characteristics of DNA underreplication zone in the 75C region of intercalary heterochromatin in Drosophila melanogaster polytene chromosomes</title>
            <link>http://www.medworm.com/index.php?rid=2707989&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fqt0022g4k1pw3580%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In Drosophila polytene chromosomes, regions of intercalary heterochromatin are scattered throughout the euchromatic arms. Here, we present
 data on the first fine analysis of the individual intercalary heterochromatin region, 75C1-2, located in the 3L chromosome.
 By using electron microscopy, we demonstrated that this region appears as three closely adjacent condensed bands. Mapping
 of the region on the physical map by means of the chromosomal rearrangements with known breakpoints showed that the length
 of the region is about 445&amp;nbsp;kb. Although it seems that the SUUR protein binds to the whole 75C1-2 region, the proximal part
 of the region is fully polytenized, so the DNA underreplication zone is asymmetric and located in the distal half of the region.
 Finally, ...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2707989</comments>
            <pubDate>Fri, 14 Aug 2009 17:47:29 +0100</pubDate>
            <guid isPermaLink="false">2707989</guid>        </item>
        <item>
            <title>Spatial link between nucleoli and expression of the Zac1 gene</title>
            <link>http://www.medworm.com/index.php?rid=2666400&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc98701v66m148834%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Eukaryotic genomes are highly organized within the cell nucleus. Genome organization not only implies the preferential positioning
 of genetic elements in the interphase nucleus but also the topographic distribution of biological processes. We have investigated
 the relationship between spatial organization and genome function in single cells. Myc, c-Met, Igf2r, Asb4, and Zac1 genes have the same radial distribution, but they are not positioned in close proximity with respect to each other. Three-dimensional
 mapping of their transcription sites uncovered a gene-specific pattern of relative positioning with respect to the nucleolus.
 We found that the Zac1 gene transcription preferentially occurs juxtaposed to the nucleolus, and that its mRNA accumulates at this site of...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2666400</comments>
            <pubDate>Fri, 31 Jul 2009 19:47:56 +0100</pubDate>
            <guid isPermaLink="false">2666400</guid>        </item>
        <item>
            <title>Meiotic behavior of aneuploid chromatin in mouse models of Down syndrome</title>
            <link>http://www.medworm.com/index.php?rid=2662229&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp352u36226606013%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Aneuploidy, which leads to unpaired chromosomal axes during meiosis, is frequently accompanied by infertility. We previously
 showed, using three mouse models of Down syndrome, that it is an extra chromosome, but not extra gene dose, that is associated
 with male infertility and virtual absence of post-meiotic gem cells. Here, we test the hypothesis that aneuploid segments
 are differentially modified and expressed during meiosis, depending on whether they are present as an extra chromosome or
 not. In all three models examined, the trisomic region lacks a pairing partner, but in one case, spermatocytes have an extra
 (and unpaired) chromosome, while the two other models involve translocation of the trisomic region rather than an extra chromosome.
 An extra unpaired chr...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2662229</comments>
            <pubDate>Wed, 29 Jul 2009 07:16:43 +0100</pubDate>
            <guid isPermaLink="false">2662229</guid>        </item>
        <item>
            <title>The amount of heterochromatic proteins in the egg is correlated with sex determination in Planococcus citri (Homoptera, Coccoidea)</title>
            <link>http://www.medworm.com/index.php?rid=2652699&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv6160m011n872746%2F</link>
            <description>We report here that egg cells of aged females show
 larger amounts of HP1 and Su(Var)3–9 than egg cells of young females. These data suggest that a determinant of sex may be
 the amount of maternally derived heterochromatic proteins.
 
	Content Type Journal ArticleCategory Research ArticleDOI 10.1007/s00412-009-0231-7Authors
		Giovanni Luigi Buglia, University of Rome “La Sapienza” Department of Genetics and Molecular Biology P.le A. Moro 5 00185 Rome ItalyDaniela Dionisi, University of Rome “La Sapienza” Department of Genetics and Molecular Biology P.le A. Moro 5 00185 Rome ItalyMarina Ferraro, University of Rome “La Sapienza” Department of Genetics and Molecular Biology P.le A. Moro 5 00185 Rome Italy
	

	
		Journal ChromosomaOnline ISSN 1432-0886Print ISSN 0009-5915 (Sourc...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2652699</comments>
            <pubDate>Mon, 27 Jul 2009 21:50:09 +0100</pubDate>
            <guid isPermaLink="false">2652699</guid>        </item>
        <item>
            <title>Persistent mechanical linkage between sister chromatids throughout anaphase</title>
            <link>http://www.medworm.com/index.php?rid=2639411&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F471w7u712158n627%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In budding yeast, we have found that sister rDNA arrays marked with fluorescent probes can be visualized as two distinguishable
 strands during metaphase. Upon anaphase, these arm loci are drawn into the spindle, where they adopt a cruciform-like structure
 and stretch 2.5-fold as they migrate to the poles. Therefore, while sister rDNA arrays appear separated in metaphase, mechanical
 linkages between sister arm loci persist throughout anaphase in yeast, as shown in grasshopper spermatocytes (Paliulis and
 Nicklas 2004). These linkages are partially dependent on the protector of cohesin, SGO1. In anaphase, the spatially regulated dissolution
 of these mechanical linkages serves to prevent premature sister separation and restrain the rate of spindle elongation. Thus,
 si...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2639411</comments>
            <pubDate>Thu, 23 Jul 2009 09:00:33 +0100</pubDate>
            <guid isPermaLink="false">2639411</guid>        </item>
        <item>
            <title>Site-specifically phosphorylated forms of H1.5 and H1.2 localized at distinct regions of the nucleus are related to different processes during the cell cycle</title>
            <link>http://www.medworm.com/index.php?rid=2633263&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq35447735r324251%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The cell cycle-associated phosphorylation of histone H1.5 is manifested as three discrete phosphorylated forms, occurring
 exclusively on Ser17, Ser172, and Ser188 during interphase. During late G2 and mitosis the up-phosphorylation occurs exclusively on threonine at either Thr137 or Thr154 to build the tetraphosphorylated forms of H1.5, whereas the pentaphosphorylated forms result from phosphorylation at Thr10. To determine the kinetic and spatial distribution of histone H1 phosphorylation within the nucleus of synchronized Hela
 cells we localized three distinct phosphorylation sites of histone subtype H1.5 using affinity-purified polyclonal antibodies
 generated against phosphorylated Ser17, Ser172, and Thr10. Immunofluorescence labeling of synchronized HeLa cells us...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2633263</comments>
            <pubDate>Sat, 18 Jul 2009 08:27:33 +0100</pubDate>
            <guid isPermaLink="false">2633263</guid>        </item>
        <item>
            <title>At the right place at the right time: novel CENP-A binding proteins shed light on centromere assembly</title>
            <link>http://www.medworm.com/index.php?rid=2592847&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq4kx184v53774748%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Centromeres, the chromosomal loci that form the sites of attachment for spindle microtubules during mitosis, are identified
 by a unique chromatin structure generated by nucleosomes containing the histone H3 variant CENP-A. The apparent epigenetic
 mode of centromere inheritance across mitotic and meiotic divisions has generated much interest in how CENP-A assembly occurs
 and how structurally divergent centromeric nucleosomes can specify the centromere complex. Although a substantial number of
 proteins have been implicated in centromere assembly, factors that can bind CENP-A specifically and deliver nascent protein
 to the centromere were, thus far, lacking. Several recent reports on experiments in fission yeast and human cells have now
 shown significant progress on ...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2592847</comments>
            <pubDate>Fri, 10 Jul 2009 08:10:19 +0100</pubDate>
            <guid isPermaLink="false">2592847</guid>        </item>
        <item>
            <title>The spatial repositioning of adipogenesis genes is correlated with their expression status in a porcine mesenchymal stem cell adipogenesis model system</title>
            <link>http://www.medworm.com/index.php?rid=2592848&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fnu8582q215g73681%2F</link>
            <description>In this study, we
 have examined the genome organization in interphase nuclei during adipogenesis, using the pig as a model organism. We hypothesized
 that changes in the gene expression profile and chromatin remodeling which occur during cellular differentiation would elicit
 repositioning of whole chromosomes, moving specific genes on them to different regions of the nucleus. We established an in
 vitro adipogenesis differentiation system using mesenchymal stem cells, derived from porcine bone marrow. The nuclear position
 of seven adipogenesis genes (PPARG, SREBF1, FABP4, CEBPA, CEBPB, CREB, and GATA2), two control genes (SOX9 and MYL1), and six chromosomes carrying these gene loci (SSC4, SSC6, SSC12, SSC13, SSC15, and SSC17) was determined. We found that
 during adipogenesis, using the...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2592848</comments>
            <pubDate>Thu, 09 Jul 2009 12:11:57 +0100</pubDate>
            <guid isPermaLink="false">2592848</guid>        </item>
        <item>
            <title>Zeste can facilitate long-range enhancer–promoter communication and insulator bypass in Drosophila melanogaster</title>
            <link>http://www.medworm.com/index.php?rid=2590478&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fwp722p29m75g4x70%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The looping model of enhancer–promoter interactions predicts that these specific long-range interactions are supported by
 a certain class of proteins. In particular, the Drosophila transcription factor Zeste was hypothesized to facilitate long-distance associations between enhancers and promoters. We
 have re-examined the role of Zeste in supporting long-range interactions between an enhancer and a promoter using the white gene as a model system. The results show that Zeste binds to the upstream white promoter region and the enhancer that is responsible for white activation in the eyes. We have confirmed the previous finding that Zeste is not required for the activity of the eye enhancer
 and the promoter when they are located in close proximity to each other. Howeve...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2590478</comments>
            <pubDate>Mon, 06 Jul 2009 20:15:11 +0100</pubDate>
            <guid isPermaLink="false">2590478</guid>        </item>
        <item>
            <title>Rye B chromosomes are weakly transcribed and might alter the transcriptional activity of A chromosome sequences</title>
            <link>http://www.medworm.com/index.php?rid=2579224&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh5u725723u400167%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;B chromosomes (Bs) are dispensable components of the genomes of numerous species. To test whether the transcriptome of a host
 is influenced by Bs, we looked for differences in expression in response to additional Bs. Comparative complementary DNA amplified
 fragment length polymorphism experiments resulted in the identification of 16 putative B-chromosome-associated transcripts.
 This comprises 0.7% of the total transcript number and indicates a low activity of Bs. We also provide evidence that B chromosome
 influences in trans the transcription of A chromosome sequences. The B-specific transcribed sequences B1334, B8149, and B2465 belong to high-copy
 families with similarity to mobile elements. For all analyzed B-chromosome-derived transcripts, similar A chromosome-e...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2579224</comments>
            <pubDate>Mon, 06 Jul 2009 16:51:04 +0100</pubDate>
            <guid isPermaLink="false">2579224</guid>        </item>
        <item>
            <title>Synaptonemal complex assembly and H3K4Me3 demethylation determine DIDO3 localization in meiosis</title>
            <link>http://www.medworm.com/index.php?rid=2550004&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F65426n0472754718%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Synapsis of homologous chromosomes is a key meiotic event, mediated by a large proteinaceous structure termed the synaptonemal
 complex. Here, we describe a role in meiosis for the murine death-inducer obliterator (Dido) gene. The Dido gene codes for three proteins that recognize trimethylated histone H3 lysine 4 through their amino-terminal plant homeodomain
 domain. DIDO3, the largest of the three isoforms, localizes to the central region of the synaptonemal complex in germ cells.
 DIDO3 follows the distribution of the central region protein SYCP1 in Sycp3−/− spermatocytes, which lack the axial elements of the synaptonemal complex. This indicates that synapsis is a requirement
 for DIDO3 incorporation. Interestingly, DIDO3 is missing from the synaptonemal complex ...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2550004</comments>
            <pubDate>Fri, 26 Jun 2009 07:12:48 +0100</pubDate>
            <guid isPermaLink="false">2550004</guid>        </item>
        <item>
            <title>Cohesin gene defects may impair sister chromatid alignment and genome stability in Arabidopsis thaliana</title>
            <link>http://www.medworm.com/index.php?rid=2500641&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fajl3208n74308833%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In contrast to yeast, plant interphase nuclei often display incomplete alignment (cohesion) along sister chromatid arms. Sister
 chromatid cohesion mediated by the multi-subunit cohesin complex is essential for correct chromosome segregation during nuclear
 divisions and for DNA recombination repair. The cohesin complex consists of the conserved proteins SMC1, SMC3, SCC3, and an
 α-kleisin subunit. Viable homozygous mutants could be selected for the Arabidopsis thaliana α-kleisins SYN1, SYN2, and SYN4, which can partially compensate each other. For the kleisin SYN3 and for the single-copy genes SMC1, SMC3, and SCC3, only heterozygous mutants were obtained that displayed between 77% and 97% of the wild-type transcript level. Compared to
 wild-type nuclei, sister chroma...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2500641</comments>
            <pubDate>Wed, 17 Jun 2009 07:05:37 +0100</pubDate>
            <guid isPermaLink="false">2500641</guid>        </item>
        <item>
            <title>Nuclear envelope-limited chromatin sheets (ELCS) and heterochromatin higher order structure</title>
            <link>http://www.medworm.com/index.php?rid=2500642&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F651145wur2378246%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The interphase nucleus and nuclear envelope can acquire a myriad of shapes in normal or pathological cell states. There exist
 a wide variety of indentations and invaginations, of protrusions and evaginations. It has been difficult to classify and name
 all of these nuclear shapes and, consequently, a barrier to understanding the biochemical and biophysical causes. This review
 focuses upon one type of nuclear envelope shape change, named “nuclear envelope-limited chromatin sheets” (ELCS), which appears
 to involve exaggerated nuclear envelope growth, carrying with it one or more layers of ∼30&amp;nbsp;nm diameter heterochromatin. A
 hypothesis on the formation of ELCS is proposed, relating higher order heterochromatin structure in an interphase nucleus,
 nuclear enve...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2500642</comments>
            <pubDate>Fri, 12 Jun 2009 10:43:57 +0100</pubDate>
            <guid isPermaLink="false">2500642</guid>        </item>
        <item>
            <title>DNA methylation and methyl-CpG binding proteins: developmental requirements and function</title>
            <link>http://www.medworm.com/index.php?rid=2500643&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr072181747625001%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;DNA methylation is a major epigenetic modification in the genomes of higher eukaryotes. In vertebrates, DNA methylation occurs
 predominantly on the CpG dinucleotide, and approximately 60% to 90% of these dinucleotides are modified. Distinct DNA methylation
 patterns, which can vary between different tissues and developmental stages, exist on specific loci. Sites of DNA methylation
 are occupied by various proteins, including methyl-CpG binding domain (MBD) proteins which recruit the enzymatic machinery
 to establish silent chromatin. Mutations in the MBD family member MeCP2 are the cause of Rett syndrome, a severe neurodevelopmental
 disorder, whereas other MBDs are known to bind sites of hypermethylation in human cancer cell lines. Here, we review the advances
 in our...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2500643</comments>
            <pubDate>Tue, 09 Jun 2009 12:43:30 +0100</pubDate>
            <guid isPermaLink="false">2500643</guid>        </item>
        <item>
            <title>Cohesin axis maturation and presence of RAD51 during first meiotic prophase in a true bug</title>
            <link>http://www.medworm.com/index.php?rid=2462381&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy734t77024074676%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We have analyzed in a true bug, Graphosoma italicum (Pentatomidae, Hemiptera), the temporal and functional relationships between recombination events, synapsis progression,
 and SMC1α and SMC3 cohesin axis maturation throughout the male first meiotic prophase. The localization of the histone variant
 histone H3 trimethylated at lysine 9 at chromosome ends has allowed us to determine the association of these heterochromatic
 domains through prophase I stages. Results highlighted that cohesins provide to be good markers for synapsis progression since
 the formation, morphology, and development of the SMC1α and SMC3 cohesin axes resemble the synaptonemal complex dynamics and,
 also, that in this species the initiation of recombination precedes synapsis. In addition, we h...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2462381</comments>
            <pubDate>Thu, 04 Jun 2009 10:05:40 +0100</pubDate>
            <guid isPermaLink="false">2462381</guid>        </item>
        <item>
            <title>In memoriam—Crodowaldo Pavan</title>
            <link>http://www.medworm.com/index.php?rid=2445628&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0775w54473162421%2F</link>
            <description>Content Type Journal ArticleCategory ObituaryDOI 10.1007/s00412-009-0217-5Authors
		Eduardo Gorab, Universidade de São Paulo Departamento de Genética e Biologia Evolutiva, Instituto de Biociências Rua do Matão 277, Cidade Universitária São Paulo São Paulo 05508-090 Brazil
	

	
		Journal ChromosomaOnline ISSN 1432-0886Print ISSN 0009-5915 (Source: Chromosoma)</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2445628</comments>
            <pubDate>Fri, 29 May 2009 08:16:28 +0100</pubDate>
            <guid isPermaLink="false">2445628</guid>        </item>
        <item>
            <title>Epigenetic marks for chromosome imprinting during spermatogenesis in coccids</title>
            <link>http://www.medworm.com/index.php?rid=2431435&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm3h8071041h5056p%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The establishment of sex-specific epigenetic marks during gametogenesis is one of the key feature of genomic imprinting. By
 immunocytological analysis, we thoroughly characterized the chromatin remodeling events that take place during gametogenesis
 in the mealybug Planococcus citri, in which an entire haploid set of (imprinted) chromosomes undergoes facultative heterochromatinization in male embryos.
 Building on our previous work, we have investigated the interplay of several epigenetic marks in the regulation of this genome-wide
 phenomenon. We characterized the germline patterns of histone modifications, Me(3)K9H3, Me(2)K9H3, and Me(3)K20H4, and of
 heterochromatic proteins, PCHET2 (HP1-like) and HP2-like during male and female gametogenesis. We found that at all s...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2431435</comments>
            <pubDate>Thu, 21 May 2009 06:15:54 +0100</pubDate>
            <guid isPermaLink="false">2431435</guid>        </item>
        <item>
            <title>Molecular cloning and characterization of the germline-restricted chromosome sequence in the zebra finch</title>
            <link>http://www.medworm.com/index.php?rid=2426456&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv8803jx203r24577%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The zebra finch (Taeniopygia guttata) germline-restricted chromosome (GRC) is the largest chromosome and has a unique system of transmission in germ cells. In
 the male, the GRC exists as a single heterochromatic chromosome in the germline and is eliminated from nuclei in late spermatogenesis.
 In the female, the GRC is bivalent and euchromatic and experiences recombination. These characteristics suggest a female-specific
 or female-beneficial function of the GRC. To shed light on the function of GRC, we cloned a portion of the GRC using random
 amplified polymorphic DNA–polymerase chain reaction and analyzed it using molecular genetic and cytogenetic methods. The GRC
 clone hybridized strongly to testis but not blood DNA in genomic Southern blots. In fluorescent in s...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2426456</comments>
            <pubDate>Tue, 19 May 2009 05:54:48 +0100</pubDate>
            <guid isPermaLink="false">2426456</guid>        </item>
        <item>
            <title>Constitutive heterochromatin: a surprising variety of expressed sequences</title>
            <link>http://www.medworm.com/index.php?rid=2395713&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk33512w631767766%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The organization of chromosomes into euchromatin and heterochromatin is amongst the most important and enigmatic aspects of
 genome evolution. Constitutive heterochromatin is a basic yet still poorly understood component of eukaryotic chromosomes,
 and its molecular characterization by means of standard genomic approaches is intrinsically difficult. Although recent evidence
 indicates that the presence of transcribed genes in constitutive heterochromatin is a conserved trait that accompanies the
 evolution of eukaryotic genomes, the term heterochromatin is still considered by many as synonymous of gene silencing. In
 this paper, we comprehensively review data that provide a clearer picture of transcribed sequences within constitutive heterochromatin,
 with a special emp...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2395713</comments>
            <pubDate>Sat, 02 May 2009 06:24:59 +0100</pubDate>
            <guid isPermaLink="false">2395713</guid>        </item>
        <item>
            <title>GAL4 induces transcriptionally active puff in the absence of dSAGA- and ATAC-specific chromatin acetylation in the Drosophila melanogaster polytene chromosome</title>
            <link>http://www.medworm.com/index.php?rid=2395712&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu357057481167476%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Puffs in the polytene chromosome of Drosophila melanogaster are characteristic of sites of high-level active transcription which can be observed directly under the microscope. We studied
 the dependence of puff formation on chromatin modifications at a site where a GAL4-inducible transgene is located in the 61C7
 cytological region. Immunostaining of salivary gland polytene chromosomes indicated no increase of either dSAGA-specific histone
 H3 lysine 14, or ATAC-specific histone H4 lysine 5 and 12 acetylation in the puffed region. Nor did we observe increased levels
 of H4K8ac, H3K18ac, or H4K16ac in the puff. In accordance with the above, puff formation as well as localization of Pol II
 and GAL4 was detectable at the 61C region in dAda2b and dAda2a null homozygotes, w...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2395712</comments>
            <pubDate>Sat, 02 May 2009 06:24:59 +0100</pubDate>
            <guid isPermaLink="false">2395712</guid>        </item>
        <item>
            <title>Cajal’s contribution to the knowledge of the neuronal cell nucleus</title>
            <link>http://www.medworm.com/index.php?rid=2385775&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn57667t10476x2m2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In 1906, the Spanish neurobiologist Santiago Ramón y Cajal was awarded the Nobel Prize in Physiology or Medicine in recognition
 of his work on the structure of neurons and their connections. Cajal is commonly regarded as the father of modern neuroscience.
 What is less well known is that Cajal also had a great interest in intracellular neuronal structures and developed the reduced
 silver nitrate method for the study of neurofibrils (neurofilaments) and nuclear subcompartments. It was in 1903 that Cajal
 discovered the “accessory body” (“Cajal body”) and seven years later, published an article on the organization of the cell
 nucleus in mammalian neurons that represents a masterpiece of nuclear structure at the light microscopy level. In addition
 to the acces...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2385775</comments>
            <pubDate>Thu, 30 Apr 2009 06:03:18 +0100</pubDate>
            <guid isPermaLink="false">2385775</guid>        </item>
        <item>
            <title>Distinct acetylation of Trypanosoma cruzi histone H4 during cell cycle, parasite differentiation, and after DNA damage</title>
            <link>http://www.medworm.com/index.php?rid=2373486&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff18054278l575477%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Histones of trypanosomes are quite divergent when compared to histones of most eukaryotes. Nevertheless, the histone H4 of
 Trypanosoma cruzi, the protozoan that causes Chagas’ disease, is acetylated in the N terminus at lysines 4, 10, and 14. Here, we investigated
 the cellular distribution of histone H4 containing each one of these posttranslational modifications by using specific antibodies.
 Histone H4 acetylated at lysine 4 (H4-K4ac) is found in the entire nuclear space preferentially at dense chromatin regions,
 excluding the nucleolus of replicating epimastigote forms of the parasite. In contrast, histone H4 acetylated either at K10
 or K14 is found at dispersed foci all over the nuclei and at the interface between dense and nondense chromatin areas as observed...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2373486</comments>
            <pubDate>Sat, 25 Apr 2009 07:28:07 +0100</pubDate>
            <guid isPermaLink="false">2373486</guid>        </item>
        <item>
            <title>Meiotic localization of Mre11 and Rad50 in wild type, spo11-1, and MRN complex mutants of Coprinus cinereus</title>
            <link>http://www.medworm.com/index.php?rid=2373487&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F710230t10314r625%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The Mre11-Rad50-Nbs1 (MRN) complex is required for numerous cellular processes that involve interactions with DNA double-strand
 breaks. For the majority of these processes, the MRN complex is thought to act as a unit, with each protein aiding the activity
 of the others. We have examined the relationship between Mre11 and Rad50 during meiosis in the basidiomycete Coprinus cinereus (Coprinopsis cinerea), investigating to what extent activities of Mre11 and Rad50 are interdependent. We showed that mre11-1 is epistatic to rad50-1 with respect to the time of meiotic arrest, indicating that Mre11 activity facilitates the diffuse diplotene arrest of rad50 mutants. Anti-Mre11 and anti-Rad50 antibodies were used to examine MRN complex localization in a wild-type strain and in
...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2373487</comments>
            <pubDate>Sat, 25 Apr 2009 07:28:06 +0100</pubDate>
            <guid isPermaLink="false">2373487</guid>        </item>
        <item>
            <title>An elegant miRror: microRNAs in stem cells, developmental timing and cancer</title>
            <link>http://www.medworm.com/index.php?rid=2321229&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy38376216137p471%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;MicroRNAs (miRNAs) were first discovered in genetic screens for regulators of developmental timing in the stem-cell-like seam
 cell lineage in Caenorhabditis elegans. As members of the heterochronic pathway, the lin-4 and let-7 miRNAs are required in the seam cells for the correct progression of stage-specific events and to ensure that cell cycle
 exit and terminal differentiation occur at the correct time. Other heterochronic genes such as lin-28 and lin-41 are direct targets of the lin-4 and let-7 miRNAs. Recent findings on the functions of the let-7 and lin-4/mir-125 miRNA families and lin-28 and lin-41 orthologs from a variety of organisms suggest that core elements of the heterochronic pathway are retained in mammalian stem
 cells and development. In particular, th...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2321229</comments>
            <pubDate>Thu, 02 Apr 2009 05:51:20 +0100</pubDate>
            <guid isPermaLink="false">2321229</guid>        </item>
        <item>
            <title>The Mi-2/NuRD complex associates with pericentromeric heterochromatin during S phase in rapidly proliferating lymphoid cells</title>
            <link>http://www.medworm.com/index.php?rid=2281686&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw4278w42m1862u22%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Chromosomal replication results in the duplication not only of DNA sequence but also of the patterns of histone modification,
 DNA methylation, and nucleoprotein structure that constitute epigenetic information. Pericentromeric heterochromatin in human
 cells is characterized by unique patterns of histone and DNA modification. Here, we describe association of the Mi-2/NuRD
 complex with specific segments of pericentromeric heterochromatin consisting of Satellite II/III DNA located on human chromosomes
 1, 9, and 16 in some but not all cell types. This association is linked in part to DNA replication and chromatin assembly
 and may suggest a role in these processes. Mi-2/NuRD accumulation is independent of Polycomb association and is characterized
 by a unique pattern of...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2281686</comments>
            <pubDate>Fri, 20 Mar 2009 09:53:08 +0100</pubDate>
            <guid isPermaLink="false">2281686</guid>        </item>
        <item>
            <title>Chromatin dynamics is correlated with replication timing</title>
            <link>http://www.medworm.com/index.php?rid=2281687&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fvtp38770814q5153%2F</link>
            <description>In this study, a bio-computational approach is employed to simultaneously measure
 the translational motion of large populations of ChrD in the cell nucleus of living cells. Both movement and configurational
 changes are strikingly higher in early S-phase replicating ChrD compared to those that replicate in mid and late S-phase.
 The chromatin dynamics was not sensitive to transcription inhibition by α-amanitin but was significantly reduced by actinomycin
 D treatment. Since a majority of active genes replicate in early S-phase, our results suggest a correlation between levels
 of chromatin dynamics and chromatin poised for active transcription. Analysis of ChrD colocalization with transcription sites
 and cDNA with ChrD and transcription sites further supports this proposal.
 
	Content T...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2281687</comments>
            <pubDate>Fri, 20 Mar 2009 09:53:06 +0100</pubDate>
            <guid isPermaLink="false">2281687</guid>        </item>
        <item>
            <title>2C or not 2C: a closer look at cell nuclei and their DNA content</title>
            <link>http://www.medworm.com/index.php?rid=2221391&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl165660728242321%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The life cycle of animals and plants involves changes in chromosome number (nuclear phase) and sometimes even the karyotype,
 and consequently the DNA content of a nuclear genome is not static in time. Thus, in order to interpret DNA content data,
 it is important that the status of the materials from which DNA content is estimated be precisely defined. The previously
 proposed distinction between “holoploid” (C) and “monoploid” (Cx) genome size covers the most frequent states of plant and
 animal nuclear genomes. However, restricting nomenclature to just C and Cx still leaves a number of unresolved problems. Here,
 we propose an extension of the C-value terminology to handle a range of cytogenetic conditions, life cycle segments, and nuclear
 phases. A set of s...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2221391</comments>
            <pubDate>Thu, 26 Feb 2009 10:34:22 +0100</pubDate>
            <guid isPermaLink="false">2221391</guid>        </item>
        <item>
            <title>Monoallelic gene expression in mammals</title>
            <link>http://www.medworm.com/index.php?rid=2221392&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc26u20u01l6v734q%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Three systems of monoallelic gene expression in mammals are known, namely, X-chromosome inactivation, imprinting, and allelic
 exclusion. In all three systems, monoallelic expression is regulated epigenetically and is frequently directed by long non-coding
 RNAs (ncRNAs). This review briefs all three systems of monoallelic gene expression in mammals focusing on chromatin modifications,
 spatial chromosome organization in the nucleus, and the functioning of ncRNAs.
 
	Content Type Journal ArticleCategory ReviewDOI 10.1007/s00412-009-0206-8Authors
		Irina S. Zakharova, Russian Academy of Sciences Siberian Department, Institute of Cytology and Genetics Novosibirsk RussiaAlexander I. Shevchenko, Russian Academy of Sciences Siberian Department, Institute of Cytology and Gene...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2221392</comments>
            <pubDate>Thu, 26 Feb 2009 10:34:21 +0100</pubDate>
            <guid isPermaLink="false">2221392</guid>        </item>
        <item>
            <title>Relationship between incomplete synapsis and chiasma localization</title>
            <link>http://www.medworm.com/index.php?rid=2215556&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fju7685636l291331%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;One of the subjects within the meiotic field that has been actively investigated in the recent years is the temporal and functional
 relationships between meiotic recombination, cohesin loading and synaptonemal complex (SC) assembly. Although the study of
 meiotic mutants has shed some light, many questions remain to be answered. Here, we have studied this topic in the orthopteran
 Paratettix meridionalis, a species with telocentric chromosomes, which shows two unusual cytological features: pairing and synapsis of homologues
 during prophase I are restricted to the non-centromeric distal regions and extremely distal chiasma localization in metaphase
 I bivalents. In order to determine whether there is a relationship between both phenomena, we have used: (1) a spreading ...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2215556</comments>
            <pubDate>Tue, 24 Feb 2009 09:44:38 +0100</pubDate>
            <guid isPermaLink="false">2215556</guid>        </item>
        <item>
            <title>Two new chromodomain-containing proteins that associate with heterochromatin in Sciara coprophila chromosomes</title>
            <link>http://www.medworm.com/index.php?rid=2500644&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu3t05w41j67w2831%2F</link>
            <description>We report here the molecular and cytological characterization of two proteins, ScoHET1 and ScoHET2 (for Sciara coprophila heterochromatin), which associate to constitutive heterochromatin in the dipteran S. coprophila. Both proteins, ScoHET1 of 37&amp;nbsp;kDa and ScoHET2 of 44&amp;nbsp;kDa, display two chromodomain motifs that contain the conserved residues
 essential for the recognition of methylated histone H3 at lysine 9. We raised antibodies to analyze the chromosomal location
 of ScoHET1 and ScoHET2 in somatic and germline cells. In S. coprophila polytene chromosomes, both proteins associate to the pericentromeric regions and to the heterochromatic subterminal bands
 of the chromosomes. In germinal nuclei, ScoHET1 and ScoHET2 proteins distribute to the heterochromatic regions of the regular
...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2500644</comments>
            <pubDate>Wed, 11 Feb 2009 06:57:02 +0100</pubDate>
            <guid isPermaLink="false">2500644</guid>        </item>
        <item>
            <title>Two new chromodomain-containing proteins that associate with heterochromatin in 
 Sciara coprophila
 chromosomes</title>
            <link>http://www.medworm.com/index.php?rid=2181533&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu3t05w41j67w2831%2F</link>
            <description>We report here the molecular and cytological characterization of two proteins, ScoHET1 and ScoHET2 (for Sciara coprophila heterochromatin), which associate to constitutive heterochromatin in the dipteran S. coprophila. Both proteins, ScoHET1 of 37&amp;nbsp;kDa and ScoHET2 of 44&amp;nbsp;kDa, display two chromodomain motifs that contain the conserved residues
 essential for the recognition of methylated histone H3 at lysine 9. We raised antibodies to analyze the chromosomal location
 of ScoHET1 and ScoHET2 in somatic and germline cells. In S. coprophila polytene chromosomes, both proteins associate to the pericentromeric regions and to the heterochromatic subterminal bands
 of the chromosomes. In germinal nuclei, ScoHET1 and ScoHET2 proteins distribute to the heterochromatic regions of the regular
...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2181533</comments>
            <pubDate>Wed, 11 Feb 2009 06:57:02 +0100</pubDate>
            <guid isPermaLink="false">2181533</guid>        </item>
        <item>
            <title>Parental genomes mix in mule and human cell nuclei</title>
            <link>http://www.medworm.com/index.php?rid=2171999&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1342m1n1n4358g85%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Whether chromosome sets inherited from father and mother occupy separate spaces in the cell nucleus is a question first asked
 over 110&amp;nbsp;years ago. Recently, the nuclear organization of the genome has come increasingly into focus as an important level
 of epigenetic regulation. In this context, it is indispensable to know whether or not parental genomes are spatially separated.
 Genome separation had been demonstrated for plant hybrids and for the early mammalian embryo. Conclusive studies for somatic
 mammalian cell nuclei are lacking because homologous chromosomes from the two parents cannot be distinguished within a species.
 We circumvented this problem by investigating the three-dimensional distribution of chromosomes in mule lymphocytes and fibroblasts.
 Genom...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2171999</comments>
            <pubDate>Sat, 07 Feb 2009 10:09:46 +0100</pubDate>
            <guid isPermaLink="false">2171999</guid>        </item>
        <item>
            <title>Cloning and sequencing of the breakpoint regions of inversion 5g fixed in Drosophila buzzatii</title>
            <link>http://www.medworm.com/index.php?rid=3095607&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8627n084hh3564q0%2F</link>
            <description>In this study, we have characterized the breakpoint regions of inversion 5g, fixed in D. buzzatii and absent in Drosophila koepferae and other closely related species. A novel approach comprising four experimental steps was used. First, D. buzzatii BAC clones encompassing the breakpoints were identified and their ends sequenced. Then, breakpoint regions were mapped at
 high resolution in the Drosophila mojavensis genome sequence. Finally, breakpoint regions were isolated by polymerase chain reaction in D. buzzatii and D. koepferae and sequenced. Our aim was to shed light on the mechanism that generated inversion 5g and specifically to test for an implication of the transposon Galileo. No evidence implicates Galileo or other transposable elements in the origin of inversion 5g that was gener...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3095607</comments>
            <pubDate>Sat, 07 Feb 2009 10:09:44 +0100</pubDate>
            <guid isPermaLink="false">3095607</guid>        </item>
        <item>
            <title>Cloning and sequencing of the breakpoint regions of inversion 
 5g
 fixed in 
 Drosophila buzzatii</title>
            <link>http://www.medworm.com/index.php?rid=2172000&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8627n084hh3564q0%2F</link>
            <description>In this study, we have characterized the breakpoint regions of inversion 5g, fixed in D. buzzatii and absent in Drosophila koepferae and other closely related species. A novel approach comprising four experimental steps was used. First, D. buzzatii BAC clones encompassing the breakpoints were identified and their ends sequenced. Then, breakpoint regions were mapped at
 high resolution in the Drosophila mojavensis genome sequence. Finally, breakpoint regions were isolated by polymerase chain reaction in D. buzzatii and D. koepferae and sequenced. Our aim was to shed light on the mechanism that generated inversion 5g and specifically to test for an implication of the transposon Galileo. No evidence implicates Galileo or other transposable elements in the origin of inversion 5g that was gener...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2172000</comments>
            <pubDate>Sat, 07 Feb 2009 10:09:44 +0100</pubDate>
            <guid isPermaLink="false">2172000</guid>        </item>
        <item>
            <title>In memoriam—Evgueni Ananiev</title>
            <link>http://www.medworm.com/index.php?rid=2159849&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa3601p8107633758%2F</link>
            <description>Content Type Journal ArticleCategory ObituaryDOI 10.1007/s00412-009-0202-zAuthors
		Antoni Rafalski, DuPont Co./Pioneer Hi-Bred Wilmington DE 19807 USA
	

	
		Journal ChromosomaOnline ISSN 1432-0886Print ISSN 0009-5915 (Source: Chromosoma)</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2159849</comments>
            <pubDate>Tue, 03 Feb 2009 07:15:14 +0100</pubDate>
            <guid isPermaLink="false">2159849</guid>        </item>
        <item>
            <title>Disruption of FEM1C-W gene in zebra finch: evolutionary insights on avian ZW genes</title>
            <link>http://www.medworm.com/index.php?rid=2103961&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm64v74305252v227%2F</link>
            <description>In this study, we analyzed the gene FEM1C which is highly conserved from Caenorhabditis elegans to higher vertebrates and interacts with the sex determining pathway in C. elegans. We found that FEM1C is located on the Z and W chromosome of zebra finches and probably other Passerine birds, but shows only Z linkage in other
 avian orders. In the zebra finch, FEM1C-W is degraded because of a point mutation and possibly because of loss of the first exon containing the start methionine. Thus,
 FEM1C-W appears to have degenerated or been lost from most bird species. FEM1C-Z is expressed in a cytoplasmic location in zebra finch fibroblast cells, as in C. elegans. FEM1C represents an interesting example of evolutionary degradation of a W chromosome gene.
 
	Content Type Journal ArticleCategory Res...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2103961</comments>
            <pubDate>Tue, 13 Jan 2009 08:23:56 +0100</pubDate>
            <guid isPermaLink="false">2103961</guid>        </item>
        <item>
            <title>Changes in chromatin structure correlate with transcriptional activity of nucleolar rDNA in polytene chromosomes</title>
            <link>http://www.medworm.com/index.php?rid=2032331&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft284u8t1441u0112%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Ribosomal DNA genes (rDNA) are found in tandem arrays of hundreds of repeated genes, but only a fraction of these genes are
 actively transcribed. The regulatory mechanism controlling the transition between active and inactive rDNA in higher eukaryotes
 is vital for cell survival. Here, we show that the nucleolus from Drosophila salivary gland cells contains two levels of chromatin organization reflecting differences in transcriptional activity: Decondensed
 chromatin is highly occupied with TATA-box-binding protein (TBP), phosphorylated H3S10, and acetylated H3K14, suggesting that
 rDNA in decondensed nucleolar areas is actively transcribed. Condensed chromatin lacks TBP, phosphorylated H3S10, or acetylated
 H3K14 and is enriched in the rDNA retrotransposons R1 and R2....</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2032331</comments>
            <pubDate>Wed, 10 Dec 2008 07:55:11 +0100</pubDate>
            <guid isPermaLink="false">2032331</guid>        </item>
        <item>
            <title>CAF-1 is required for efficient replication of euchromatic DNA in 
 Drosophila
 larval endocycling cells</title>
            <link>http://www.medworm.com/index.php?rid=2032330&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb417642hl4631408%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The endocycle constitutes an effective strategy for cell growth during development. In contrast to the mitotic cycle, it consists
 of multiple S-phases with no intervening mitosis and lacks a checkpoint ensuring the replication of the entire genome. Here,
 we report an essential requirement of chromatin assembly factor-1 (CAF-1) for Drosophila larval endocycles. This complex promotes histone H3–H4 deposition onto newly synthesised DNA in vitro. In metazoans, the
 depletion of its large subunit leads to the rapid accumulation of cells in S-phase. However, whether this slower S-phase progression
 results from the activation of cell cycle checkpoints or whether it reflects a more direct requirement of CAF-1 for efficient
 replication in vivo is still debated. Here, we sh...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2032330</comments>
            <pubDate>Wed, 10 Dec 2008 07:55:11 +0100</pubDate>
            <guid isPermaLink="false">2032330</guid>        </item>
        <item>
            <title>A satellite-like sequence, representing a “clone gap” in the human genome, was likely involved in the seeding of a novel centromere in macaque</title>
            <link>http://www.medworm.com/index.php?rid=2010538&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn1w3502074818233%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Although the human genome sequence is generally considered “finished”, the latest assembly (NCBI Build 36.1) still presents
 a number of gaps. Some of them are defined as “clone gaps” because they separate neighboring contigs. Evolutionary new centromeres
 are centromeres that repositioned along the chromosome, without marker order variation, during evolution. We have found that
 one human “clone gap” at 18q21.2 corresponds to an evolutionary new centromere in Old World Monkeys (OWM). The partially sequenced
 gap revealed a satellite-like structure. DNA stretches of the same satellite were found in the macaque (flanking the chromosome
 18 centromere) and in the marmoset (New World Monkey), which was used as an outgroup. These findings strongly suggested that...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2010538</comments>
            <pubDate>Tue, 02 Dec 2008 07:32:12 +0100</pubDate>
            <guid isPermaLink="false">2010538</guid>        </item>
        <item>
            <title>A centromeric DNA sequence colocalized with a centromere-specific histone H3 in tobacco</title>
            <link>http://www.medworm.com/index.php?rid=2010537&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F764434l562416660%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Centromeres play an important role in segregating chromosomes into daughter cells, and centromeric DNA assembles specific
 proteins to form a complex referred to as the kinetochore. Among these proteins, centromere-specific histone H3 (CENH3) is
 one of the most characterized and found to be located only on active centromeres. We isolated four different CENH3-coding
 complementary DNAs (cDNAs), two from Nicotiana tabaccum and one each from the ancestral diploid species, Nicotiana sylvestris and Nicotiana tomentosiformis and raised an antibody against N-terminal amino acid sequences deduced from the cDNAs. Immunostaining with the antibody revealed
 the preferential centromere localization, indicating that the cDNAs cloned in this study encode authentic tobacco CENH3. A
 ...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2010537</comments>
            <pubDate>Tue, 02 Dec 2008 07:32:12 +0100</pubDate>
            <guid isPermaLink="false">2010537</guid>        </item>
        <item>
            <title>Quantitative analysis of NOR expression in a B chromosome of the grasshopper 
 Eyprepocnemi
 s 
 ploran
 s</title>
            <link>http://www.medworm.com/index.php?rid=2010539&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe8143006l5123734%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The B24 chromosome in the Torrox population of the grasshopper Eyprepocnemis plorans is recurrently attached to a nucleolus in diplotene cells, indicating the activity of its distally located ribosomal DNA
 (rDNA). The frequency of males expressing the B chromosome nucleolus organizer region (B-NOR) almost doubled in 4&amp;nbsp;years. The
 likelihood of expressing the B-NOR increased with the B number and, in males expressing it, about 20% of their cells showed
 a nucleolus attached to the B. When active, the B-NOR contributed more than 25% of total cell nucleolar area (NA). Within
 males expressing the B-NOR, total cell NA did not differ between cells showing the active or inactive B-NOR, suggesting that
 total cell NA is tightly regulated in this species. However, this pa...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2010539</comments>
            <pubDate>Tue, 02 Dec 2008 07:32:11 +0100</pubDate>
            <guid isPermaLink="false">2010539</guid>        </item>
        <item>
            <title>Protein SYCP2 provides a link between transverse filaments and lateral elements of mammalian synaptonemal complexes</title>
            <link>http://www.medworm.com/index.php?rid=1995570&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr3j2011210736n14%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Synaptonemal complexes (SCs) are evolutionarily conserved meiosis-specific nuclear structures critically involved in synapsis,
 recombination, and segregation of homologous chromosomes. SCs are proteinaceous structures composed of (a) two lateral elements
 (LEs), to which the chromatin of the homologs is attached, (b) numerous transverse filaments (TFs) that link the LEs, and
 (c) a central element (CE). Major protein components of mammalian SCs are the TF protein SYCP1 and the LE proteins SYCP2 and
 SCYP3. How SCs become assembled is presently poorly understood, in particular, it is not known how TFs assemble at the plane
 of LEs to interconnect the homologous chromosomes. Therefore, we have investigated possible interactions between SYCP1 and
 other SC proteins. In im...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1995570</comments>
            <pubDate>Wed, 26 Nov 2008 19:58:43 +0100</pubDate>
            <guid isPermaLink="false">1995570</guid>        </item>
        <item>
            <title>RNA turnover and chromatin-dependent gene silencing</title>
            <link>http://www.medworm.com/index.php?rid=1984266&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp5714853q50t84mm%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Over the last few years, there has been a convergence of two seemingly disparate fields of study: chromatin-dependent gene
 silencing and RNA turnover. In contrast to RNA turnover mechanisms that operate on a truly posttranscriptional level, we are
 at the beginning of studies leading the way toward a model in which RNA turnover mechanisms are also involved in chromatin-dependent
 gene regulation. In particular, data from a variety of organisms have shown that the assembly of silent chromatin coincides
 with the presence or absence of non-protein-coding RNAs (ncRNAs). These range from long ncRNAs that have been classically
 implicated in the regulation of dosage compensation and genomic imprinting to small ncRNAs which are involved in heterochromatin
 assembly via the R...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1984266</comments>
            <pubDate>Fri, 21 Nov 2008 06:55:42 +0100</pubDate>
            <guid isPermaLink="false">1984266</guid>        </item>
        <item>
            <title>Artificial chromosome formation in maize (
 Zea mays
 L.)</title>
            <link>http://www.medworm.com/index.php?rid=1974198&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx878n064082r4436%2F</link>
            <description>We report on the construction of maize minichromosomes using shuttle vectors harboring native centromeric segments, origins
 of replication, selectable marker genes, and telomeric repeats. These vectors were introduced into scutellar cells of maize
 immature embryos by microprojectile bombardment. Several independent transformation events were identified containing minichromosomes
 in addition to the normal diploid complement of 20 maize chromosomes. Immunostaining indicated that the minichromosomes recruited
 centromeric protein C, which is a specific component of the centromere/kinetochore complex. Minichromosomes were estimated
 to be 15–30&amp;nbsp;Mb in size based on cytological measurements. Fluorescent in situ hybridization (FISH) showed that minichromosomes
 contain the centromeric, ...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1974198</comments>
            <pubDate>Tue, 18 Nov 2008 08:00:37 +0100</pubDate>
            <guid isPermaLink="false">1974198</guid>        </item>
        <item>
            <title>DNA bridging of yeast chromosomes VIII leads to near-reciprocal translocation and loss of heterozygosity with minor cellular defects</title>
            <link>http://www.medworm.com/index.php?rid=1974197&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7476457th18w2182%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Loss of heterozygosity (LOH) of tumor suppressor genes in somatic cells is a major process leading to several types of cancer;
 however, its underlying molecular mechanism is still poorly understood. In the present work, we demonstrate that a linear
 DNA molecule bridging two homologous chromosomes in diploid yeast cells via homologous recombination produce LOH-generating
 regions of hemizygosity by deletion. The result is a near-reciprocal translocation mutant that is characterized by slight
 cell cycle defects and increased expression of the multidrug-resistant gene VMR1. When the distance between target regions is approximately 40&amp;nbsp;kb, the specificity of gene targeting becomes less stringent
 and an ensemble of gross chromosomal rearrangements arises. These heter...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1974197</comments>
            <pubDate>Tue, 18 Nov 2008 08:00:37 +0100</pubDate>
            <guid isPermaLink="false">1974197</guid>        </item>
        <item>
            <title>ATRX marks the inactive X chromosome (Xi) in somatic cells and during imprinted X chromosome inactivation in trophoblast stem cells</title>
            <link>http://www.medworm.com/index.php?rid=1959331&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk00121284k035685%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Mammalian X chromosome inactivation (XCI) is an essential mechanism to compensate for dosage imbalances between male and female
 embryos. Although the molecular pathways are not fully understood, heterochromatinization of the Xi requires the coordinate
 recruitment of multiple epigenetic marks. Using fluorescence in situ hybridization analysis combined with immunocytochemistry,
 we demonstrate that the chromatin remodeling protein ATRX decorates the chromatids of a single, late replicating X chromosome
 in female somatic cells and co-localizes with the bona fide marker of the Xi, macroH2A1.2. Chromatin immunoprecipitation using
 somatic, embryonic stem (ES) cells and trophoblast stem (TS) cells as model for random and imprinted XCI, respectively, revealed
 that, in soma...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1959331</comments>
            <pubDate>Thu, 13 Nov 2008 15:45:16 +0100</pubDate>
            <guid isPermaLink="false">1959331</guid>        </item>
        <item>
            <title>Shugoshin regulates cohesion by driving relocalization of PP2A in Xenopus extracts</title>
            <link>http://www.medworm.com/index.php?rid=1944695&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj96g35t6128nv283%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Sister chromatid cohesion is mediated by cohesin. At the onset of mitosis, most cohesin dissociates from chromatin with the
 exception of a small population, present along chromosome arms and enriched at centromeres. A protein known as shugoshin (Sgo)
 is essential to maintain arm and centromeric cohesion until the onset of anaphase in transformed human cells, but not in other
 organisms like Drosophila or mouse. We have used Xenopus egg extracts to further explore this issue. Chromosomes assembled
 in extracts depleted of Sgo have little or no cohesin at centromeres and display centromeric cohesion defects. Unlike transformed
 human cells, however, arm cohesion is maintained in the absence of Sgo. Furthermore, Sgo depletion impairs the prophase dissociation
 of cohesin...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1944695</comments>
            <pubDate>Thu, 06 Nov 2008 07:04:43 +0100</pubDate>
            <guid isPermaLink="false">1944695</guid>        </item>
        <item>
            <title>Subnuclear compartmentalization and function of actin and nuclear Myosin I in plants</title>
            <link>http://www.medworm.com/index.php?rid=1938031&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fnl4478uu518823q7%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Actins are highly conserved proteins that serve as the basic building blocks of cytoskeletal microfilaments. In animal cells,
 specific nuclear actin adopts unconventional conformations that are involved in multiple nuclear functions and that associate
 with nuclear actin binding proteins. However, there is practically no information available about nuclear actin in plants.
 Indeed, actin has not been detected in the nuclear proteomes of many plants, and orthologs of the main structural nuclear
 actin-binding proteins have yet to be identified. Here, we have investigated the characteristics, intranuclear compartmentalization,
 and function of actin in isolated Allium cepa nuclei as well as that of its motor protein nuclear myosin I (NMI). Using conformation-specific ant...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1938031</comments>
            <pubDate>Tue, 04 Nov 2008 07:10:10 +0100</pubDate>
            <guid isPermaLink="false">1938031</guid>        </item>
        <item>
            <title>Reorganization of chromatin is an early response to nitrogen starvation in 
 Schizosaccharomyces pombe</title>
            <link>http://www.medworm.com/index.php?rid=1900331&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F45852557852220t1%2F</link>
            <description>In this study, the subnuclear localization
 of two gene clusters repressed by nitrogen was investigated. During normal growth conditions, the gene clusters localized
 to the nuclear periphery at the opposite side of the nucleus as compared to the spindle pole body. This constrained localization
 was dependent on the histone deacetylase Clr3, known to transcriptionally repress genes in these clusters. Already 20&amp;nbsp;min
 after nitrogen depletion, drastic changes in subnuclear localization of the two loci were observed, away from the NM toward
 the nuclear interior. At least for one of the clusters, the movement was clearly transcription dependent. Data presented in
 this paper illustrates how interconnected events of gene activation and nuclear reorganization are as well as provides a sugg...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1900331</comments>
            <pubDate>Tue, 21 Oct 2008 06:12:16 +0100</pubDate>
            <guid isPermaLink="false">1900331</guid>        </item>
        <item>
            <title>Chromatin: linking structure and function in the nucleolus</title>
            <link>http://www.medworm.com/index.php?rid=1887851&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F96r228660223p848%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The nucleolus is an informative model structure for studying how chromatin-regulated transcription relates to nuclear organisation.
 In this review, we describe how chromatin controls nucleolar structure through both the modulation of rDNA activity by convergently-evolved
 remodelling complexes and by direct effects upon rDNA packaging. This packaging not only regulates transcription but may also
 be important for suppressing internal recombination between tandem rDNA repeats. The identification of nucleolar histone chaperones
 and novel chromatin proteins by mass spectrometry suggests that structure-specific chromatin components remain to be characterised
 and may regulate the nucleolus in novel ways. However, it also suggests that there is considerable overlap between...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1887851</comments>
            <pubDate>Fri, 17 Oct 2008 08:51:49 +0100</pubDate>
            <guid isPermaLink="false">1887851</guid>        </item>
        <item>
            <title>Chromatin domains in higher eukaryotes: insights from genome-wide mapping studies</title>
            <link>http://www.medworm.com/index.php?rid=1879279&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw5qg7n861748j536%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In genomes of higher eukaryotes, adjacent genes often show coordinated regulation of their expression. Compartmentalization
 of multiple neighboring genes into a shared chromatin environment can facilitate this coordinated expression. New mapping
 techniques have begun to reveal that such multigene chromatin domains are a common feature of fly and mammalian genomes. Many
 different types of chromatin domains have been identified based on the genomic binding patterns of various proteins and histone
 modifications. In addition, maps of genome–nuclear lamina associations and of looping interactions between loci provide the
 first systematic views of the three-dimensional folding of interphase chromosomes. These genome-wide datasets uncover new
 architectural principles o...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1879279</comments>
            <pubDate>Tue, 14 Oct 2008 11:24:26 +0100</pubDate>
            <guid isPermaLink="false">1879279</guid>        </item>
        <item>
            <title>Coprinus cinereus
 Mer3 is required for synaptonemal complex formation during meiosis</title>
            <link>http://www.medworm.com/index.php?rid=1865063&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk87241r366g6050k%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Mer3 is an evolutionarily conserved DNA helicase that has crucial roles in meiotic recombination and crossover formation.
 We have identified the MER3 homolog in Coprinus cinereus (Ccmer3) and show that it is expressed in zygotene and pachytene meiocytes. Immunostaining analysis indicated that CcMer3 was localized
 on chromosomes at zygotene and pachytene and CcMer3 foci were more frequent on paired than unpaired chromosomes. We generated
 a C. cinereus mer3 mutant (#1) and found that it showed abnormal meiosis progression and underwent apoptosis after prophase I. Basidiospore
 production in #1 was reduced to 0.8% of the wild-type level; the spores showed slower germination at 25°C but were similar
 to the wild type at 37°C. Electron microscopic analysis of chromosome...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1865063</comments>
            <pubDate>Wed, 08 Oct 2008 12:14:03 +0100</pubDate>
            <guid isPermaLink="false">1865063</guid>        </item>
        <item>
            <title>A new class of retroviral and satellite encoded small RNAs emanates from mammalian centromeres</title>
            <link>http://www.medworm.com/index.php?rid=1865065&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr662713351177513%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The transcriptional framework of the eukaryotic centromere core has been described in budding yeast and rice, but for most
 eukaryotes and all vertebrates it remains largely unknown. The lack of large pericentric repeats in the tammar wallaby has
 made it possible to map and identify the transcriptional units at the centromere in a mammalian species for the first time.
 We show that these transcriptional units, comprised of satellites and a retrovirus, are bound by centromere proteins and that
 they are the source of a novel class of small RNA. The endogenous retrovirus from which these small RNAs are derived is now
 known to be in the centromere domain of several vertebrate classes. The discovery of this new RNA form brings together several
 independent lines of eviden...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1865065</comments>
            <pubDate>Wed, 08 Oct 2008 09:50:20 +0100</pubDate>
            <guid isPermaLink="false">1865065</guid>        </item>
        <item>
            <title>DNA demethylation: a lesson from the garden</title>
            <link>http://www.medworm.com/index.php?rid=1865064&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F28688637346r3586%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Gene silencing by DNA methylation is well documented and known to be essential for various biological phenomena in many organisms.
 In contrast, the processes that convert the silent state of a gene whose DNA is methylated and predicted to form facultative
 heterochromatin to the actively transcribed state remain elusive. In Arabidopsis, recent studies have shown that the DNA glycosylases DEMETER (DME) and REPRESSOR OF SILENCING1 (ROS1) participate in DNA
 demethylation. DME is necessary for genomic imprinting in the endosperm, while ROS1 is involved in pruning DNA methylation
 patterns in transposons and genic regions of vegetative tissues. These findings provide us with molecular clues for understanding
 the underlying mechanisms of DNA demethylation and gene activati...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1865064</comments>
            <pubDate>Wed, 08 Oct 2008 09:50:20 +0100</pubDate>
            <guid isPermaLink="false">1865064</guid>        </item>
        <item>
            <title>Promoter proximal pausing on genes in metazoans</title>
            <link>http://www.medworm.com/index.php?rid=1850358&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fwl13806508805wm2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The past two decades of research into transcriptional control of protein-encoding genes in eukaryotes have focused on regulatory
 mechanisms that act by controlling the recruitment of Pol II to a gene’s promoter. Recent genome-wide analyses of the distribution
 of Pol II indicates that Pol II is concentrated in the promoter regions of thousands of genes in human and Drosophila cells. In many cases, Pol II may have initiated transcription but paused in the promoter proximal region. Hence, release
 of Pol II from the promoter region into the body of a gene is now recognized as a common rate-limiting step in the control
 of gene expression. Notably, most genes with paused Pol II are expressed indicating that the pause can be transient. What
 causes Pol II to concentrate ...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1850358</comments>
            <pubDate>Thu, 02 Oct 2008 09:27:23 +0100</pubDate>
            <guid isPermaLink="false">1850358</guid>        </item>
        <item>
            <title>Perturbation of Incenp function impedes anaphase chromatid movements and chromosomal passenger protein flux at centromeres</title>
            <link>http://www.medworm.com/index.php?rid=1789870&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg772333619203g38%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Incenp is an essential mitotic protein that, together with Aurora B, Survivin, and Borealin, forms the core of the chromosomal
 passenger protein complex (CPC). The CPC regulates various mitotic processes and functions to maintain genomic stability.
 The proper subcellular localization of the CPC and its full catalytic activity require the presence of each core subunit in
 the complex. We have investigated the mitotic tasks of the CPC using a function blocking antibody against Incenp microinjected
 into cells at different mitotic phases. This method allowed temporal analysis of CPC functions without perturbation of complex
 assembly or activity prior to injection. We have also studied the dynamic properties of Incenp and Aurora B using fusion protein
 photobleaching. We...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1789870</comments>
            <pubDate>Thu, 11 Sep 2008 08:50:41 +0100</pubDate>
            <guid isPermaLink="false">1789870</guid>        </item>
        <item>
            <title>Linkage of 35S and 5S rRNA genes in 
 Artemisia
 (family Asteraceae): first evidence from angiosperms</title>
            <link>http://www.medworm.com/index.php?rid=1782003&amp;cid=s_33449_50_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu517x77571tm0l22%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Typically in plants, the 5S and 35S ribosomal DNA (rDNA) encoding two major ribosomal RNA species occur at separate loci.
 However, in some algae, bryophytes and ferns, they are at the same locus (linked arranged). Southern blot hybridisation, polymerase
 chain reactions (PCR), fluorescent in situ hybridisation, cloning and sequencing were used to reveal 5S and 35S rDNA genomic
 organisation in Artemisia. We observed thousands of rDNA units at two–three loci containing 5S rDNA in an inverted orientation within the inter-genic
 spacer (IGS) of 35S rDNA. The sequenced clones of 26–18S IGS from Artemisia absinthium appeared to contain a conserved 5S gene insertion proximal to the 26S gene terminus (5S rDNA-1) and a second less conserved
 5S insertion (5S rDNA-2) furthe...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1782003</comments>
            <pubDate>Tue, 09 Sep 2008 09:05:52 +0100</pubDate>
            <guid isPermaLink="false">1782003</guid>        </item>
        <item>
            <title>Higher-order genome organization in platypus and chicken sperm and repositioning of sex chromosomes during mammalian evolution</title>
            <link>http://www.medworm.com/index.php?rid=1741876&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk6971j536h7x7777%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In mammals, chromosomes occupy defined positions in sperm, whereas previous work in chicken showed random chromosome distribution.
 Monotremes (platypus and echidnas) are the most basal group of living mammals. They have elongated sperm like chicken and
 a complex sex chromosome system with homology to chicken sex chromosomes. We used platypus and chicken genomic clones to investigate
 genome organization in sperm. In chicken sperm, about half of the chromosomes investigated are organized non-randomly, whereas
 in platypus chromosome organization in sperm is almost entirely non-random. The use of genomic clones allowed us to determine
 chromosome orientation and chromatin compaction in sperm. We found that in both species chromosomes maintain orientation of
 chromosomes...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1741876</comments>
            <pubDate>Tue, 26 Aug 2008 08:16:27 +0100</pubDate>
            <guid isPermaLink="false">1741876</guid>        </item>
        <item>
            <title>The ZW sex chromosomes of 
 Gekko hokouensis
 (Gekkonidae, Squamata) represent highly conserved homology with those of avian species</title>
            <link>http://www.medworm.com/index.php?rid=1691412&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fhp77252g0v136u20%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Populations of the gecko lizard Gekko hokouensis (Gekkonidae, Squamata) on Okinawajima Island and a few other islands of the Ryukyu Archipelago, Japan, have the morphologically
 differentiated sex chromosomes, the acrocentric Z chromosome and the subtelocentric W chromosome, although the continental
 representative of this species reportedly shows no sex chromosome heteromorphism. To investigate the origin of sex chromosomes
 and the process of sex chromosomal differentiation in this species, we molecularly cloned the homologues of six chicken Z-linked
 genes and mapped them to the metaphase chromosomes of the Okinawajima sample. They were all localized to the Z and W chromosomes
 in the order ACO1/IREBP–RPS6–DMRT1–CHD1–GHR–ATP5A1, indicating that the origin o...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1691412</comments>
            <pubDate>Thu, 07 Aug 2008 09:59:44 +0100</pubDate>
            <guid isPermaLink="false">1691412</guid>        </item>
        <item>
            <title>Unexpected behavior of an inverted rye chromosome arm in wheat</title>
            <link>http://www.medworm.com/index.php?rid=1685692&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe26x31u011002756%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Distal location of chiasmata in chromosome arms is thought to be a consequence of the distal initiation of synapsis. Observations
 of meiotic behavior of a rye chromosome with an inverted arm show that patterns of chiasma distribution and frequency are
 also inverted; therefore, the patterns of synapsis and chiasma distribution are independent, and recombination frequency along
 a chromosome is position-independent and segment-specific. Since cases of random distribution of chiasmata and recombination
 are known in rye, a genetic mechanism must be present that licenses specific chromosome regions for recombination. Large differences
 in the metaphase I pairing of the inversion in various combinations of two armed and telocentric chromosomes confirm the major
 role of th...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1685692</comments>
            <pubDate>Tue, 05 Aug 2008 07:11:07 +0100</pubDate>
            <guid isPermaLink="false">1685692</guid>        </item>
        <item>
            <title>Bi-orienting chromosomes: acrobatics on the mitotic spindle</title>
            <link>http://www.medworm.com/index.php?rid=1678887&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn448425051472407%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To maintain their genetic integrity, eukaryotic cells must segregate their chromosomes properly to opposite poles during mitosis.
 This process mainly depends on the forces generated by microtubules that attach to kinetochores. During prometaphase, kinetochores
 initially interact with a single microtubule that extends from a spindle pole and then move towards a spindle pole. Subsequently,
 microtubules that extend from the other spindle pole also interact with kinetochores and, eventually, each sister kinetochore
 attaches to microtubules that extend from opposite poles (sister kinetochore bi-orientation). If sister kinetochores interact
 with microtubules in wrong orientation, this must be corrected before the onset of anaphase. Here, I discuss the processes
 leading ...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1678887</comments>
            <pubDate>Sat, 02 Aug 2008 06:54:39 +0100</pubDate>
            <guid isPermaLink="false">1678887</guid>        </item>
        <item>
            <title>Positioning of human chromosomes in murine cell hybrids according to synteny</title>
            <link>http://www.medworm.com/index.php?rid=1654912&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fgx8662622140j485%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Chromosomes occupy non-random spatial positions in interphase nuclei. It remains unclear what orchestrates this high level
 of organisation. To determine how the nuclear environment influences the spatial positioning of chromosomes, we utilised a
 panel of stable mouse hybrid cell lines carrying a single, intact human chromosome. Eleven of 22 human chromosomes revealed
 an alternative location in hybrid nuclei compared to that of human fibroblasts, with the majority becoming more internally
 localised. Human chromosomes in mouse nuclei position according to neither their gene density nor size, but rather the position
 of human chromosomes in hybrid nuclei appears to mimic that of syntenic mouse chromosomes. These results suggest that chromosomes
 adopt the behaviour of ...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1654912</comments>
            <pubDate>Thu, 24 Jul 2008 08:57:29 +0100</pubDate>
            <guid isPermaLink="false">1654912</guid>        </item>
        <item>
            <title>Spatio-temporal dynamics of replication and transcription sites in the mammalian cell nucleus</title>
            <link>http://www.medworm.com/index.php?rid=1581619&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9732p457640873nj%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To study when and where active genes replicated in early S phase are transcribed, a series of pulse-chase experiments are
 performed to label replicating chromatin domains (RS) in early S phase and subsequently transcription sites (TS) after chase
 periods of 0 to 24&amp;nbsp;h. Surprisingly, transcription activity throughout these chase periods did not show significant colocalization
 with early RS chromatin domains. Application of novel image segmentation and proximity algorithms, however, revealed close
 proximity of TS with the labeled chromatin domains independent of chase time. In addition, RNA polymerase II was highly proximal
 and showed significant colocalization with both TS and the chromatin domains. Based on these findings, we propose that chromatin
 activated f...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1581619</comments>
            <pubDate>Fri, 04 Jul 2008 05:56:03 +0100</pubDate>
            <guid isPermaLink="false">1581619</guid>        </item>
        <item>
            <title>Three-dimensional positioning of genes in mouse cell nuclei</title>
            <link>http://www.medworm.com/index.php?rid=1576946&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu13563633101521w%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To understand the regulation of the genome, it is necessary to understand its three-dimensional organization in the nucleus.
 We investigated the positioning of eight gene loci on four different chromosomes, including the β-globin gene, in mouse embryonic
 stem cells and in in vitro differentiated macrophages by fluorescence in situ hybridization on structurally preserved nuclei,
 confocal microscopy, and 3D quantitative image analysis. We found that gene loci on the same chromosome can significantly
 differ from each other and from their chromosome territory in their average radial nuclear position. Radial distribution of
 a given gene locus can change significantly between cell types, excluding the possibility that positioning is determined solely
 by the DNA sequenc...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1576946</comments>
            <pubDate>Thu, 03 Jul 2008 08:17:12 +0100</pubDate>
            <guid isPermaLink="false">1576946</guid>        </item>
        <item>
            <title>Quality control of mRNP in the nucleus</title>
            <link>http://www.medworm.com/index.php?rid=1534849&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft8365428702600k6%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Formation of functional mRNA–protein particles requires a plethora of nuclear cotranscriptional and posttranscriptional RNA
 processing and packaging steps. Faithful execution of these events is closely monitored by surveillance systems that prevent
 nuclear export of, and/or rapidly degrade, faulty transcripts. Parts of this quality control also serve to eliminate a large
 number of noncoding RNAs produced by RNA polymerase II. Here, we discuss which aberrant features trigger messenger ribonucleoprotein
 quality control, how the process is executed, and how it is connected to the transcription machinery and the nuclear pore
 complex.
 
	Content Type Journal ArticleCategory ReviewDOI 10.1007/s00412-008-0166-4Authors
		Manfred Schmid, University of Aarhus Centre for mR...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1534849</comments>
            <pubDate>Thu, 19 Jun 2008 07:01:11 +0100</pubDate>
            <guid isPermaLink="false">1534849</guid>        </item>
        <item>
            <title>Regulation of the meiotic prophase I to metaphase I transition in mouse spermatocytes</title>
            <link>http://www.medworm.com/index.php?rid=1534851&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F21621556w3k17428%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The meiotic prophase I to metaphase I transition (G2/MI) involves disassembly of synaptonemal complex (SC), chromatin condensation,
 and final compaction of morphologically distinct MI bivalent chromosomes. Control of these processes is poorly understood.
 The G2/MI transition was experimentally induced in mouse pachytene spermatocytes by okadaic acid (OA), and kinetic analysis
 revealed that disassembly of the central element of the SC occurred very rapidly after OA treatment, before histone H3 phosphorylation
 on Ser10. These events were followed by relocalization of SYCP3 and final condensation of bivalents. Enzymatic control of
 these G2/MI transition events was studied using small molecule inhibitors: butyrolactone I (BLI), an inhibitor of cyclin-dependent
 kinases...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1534851</comments>
            <pubDate>Thu, 19 Jun 2008 07:01:10 +0100</pubDate>
            <guid isPermaLink="false">1534851</guid>        </item>
        <item>
            <title>Position of human chromosomes is conserved in mouse nuclei indicating a species-independent mechanism for maintaining genome organization</title>
            <link>http://www.medworm.com/index.php?rid=1534850&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa351218011j8pn66%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The nonrandom positioning of chromosome territories in eukaryotic cells is largely correlated with gene density and is conserved
 throughout evolution. Gene-rich chromosomes are predominantly central, while gene-poor chromosomes are peripherally localized
 in interphase nuclei. We previously demonstrated that artificially introduced human chromosomes assume a position equivalent
 to their endogenous homologues in the diploid colon cancer cell line DLD-1. These chromosomal aneuploidies result in a significant
 increase in transcript levels, suggesting a relationship between genomic copy number, gene expression, and chromosome position.
 We previously proposed that each chromosome is marked by a “zip code” that determines its nonrandom position in the nucleus.
 In thi...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1534850</comments>
            <pubDate>Thu, 19 Jun 2008 07:01:10 +0100</pubDate>
            <guid isPermaLink="false">1534850</guid>        </item>
        <item>
            <title>Pontin is localized in nucleolar fibrillar centers</title>
            <link>http://www.medworm.com/index.php?rid=1517896&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk1823464w47u3hrk%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Pontin is a multifunctional protein having roles in various cellular processes including regulation of gene expression. Here,
 we addressed Pontin intracellular localization using two different monoclonal antibodies directed against different Pontin
 epitopes. For the first time, Pontin was directly visualized in nucleoli where it co-localizes with Upstream Binding Factor
 and RNA polymerase I. Nucleolar localization of Pontin was confirmed by its detection in nucleolar extracts and by electron
 microscopy, which revealed Pontin accumulation specifically in the nucleolar fibrillar centers. Pontin localization in the
 nucleolus was dynamic and Pontin accumulated in large nucleolar dots mainly during S-phase. Pontin concentration in the large
 nucleolar dots correlated wi...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1517896</comments>
            <pubDate>Thu, 12 Jun 2008 06:23:32 +0100</pubDate>
            <guid isPermaLink="false">1517896</guid>        </item>
        <item>
            <title>Classification of chromosome segregation errors in cancer</title>
            <link>http://www.medworm.com/index.php?rid=1499225&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F327q527778911m43%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Abnormal chromosome segregation at mitosis is one way by which neoplastic cells accumulate the many genetic abnormalities
 required for tumour development. In this paper, a straightforward morphology-based classification of chromosome segregation
 errors in cancer is suggested. This classification distinguishes between abnormalities in spindle symmetry (spindle multipolarity,
 size-asymmetry of ana-telophase poles) and abnormalities in sister chromatid segregation (chromosome bridges, chromatid bridges,
 chromosome lagging, acentric fragment lagging). Often, these categories of errors must be combined to accurately describe
 the events in a single abnormal mitotic cell. The suggested categories can to some extent be distinguished by standard chromatin
 staining. However...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1499225</comments>
            <pubDate>Thu, 05 Jun 2008 09:52:28 +0100</pubDate>
            <guid isPermaLink="false">1499225</guid>        </item>
        <item>
            <title>Plk1 regulates mitotic Aurora A function through βTrCP-dependent degradation of hBora</title>
            <link>http://www.medworm.com/index.php?rid=1493914&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa57717026545p04m%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Polo-like kinase 1 (Plk1) and Aurora A play key roles in centrosome maturation, spindle assembly, and chromosome segregation
 during cell division. Here we show that the functions of these kinases during early mitosis are coordinated through Bora,
 a partner of Aurora A first identified in Drosophila. Depletion of human Bora (hBora) results in spindle defects, accompanied by increased spindle recruitment of Aurora A and
 its partner TPX2. Conversely, hBora overexpression induces mislocalization of Aurora A and monopolar spindle formation, reminiscent
 of the phenotype seen in Plk1-depleted cells. Indeed, Plk1 regulates hBora. Following Cdk1-dependent recruitment, Plk1 triggers
 hBora destruction by phosphorylating a recognition site for $${\text{SCF}}^{{\text{ $ \beta $...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1493914</comments>
            <pubDate>Tue, 03 Jun 2008 06:18:55 +0100</pubDate>
            <guid isPermaLink="false">1493914</guid>        </item>
        <item>
            <title>Structure and dynamics of retrotransposons at wheat centromeres and pericentromeres</title>
            <link>http://www.medworm.com/index.php?rid=1466688&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu7x577g84655v338%2F</link>
            <description>We report the sequences of two centromere-associated
 bacterial artificial chromosome clones from a Triticum boeoticum library. Both autonomous and non-autonomous wheat centromeric retrotransposons (CRWs) were identified, both being closely associated with the centromeres of wheat. Fiber-fluorescence in situ hybridization and
 chromatin immunoprecipitation analysis showed that wheat centromeric retrotransposons (CRWs) represent a dominant component of the wheat centromere and are associated with centromere function. CRW copy number showed variation among different genomes: the D genome chromosomes contained fewer copies than either the A or B genome chromosomes. The frequency of lengthy continuous CRW arrays was higher than that in either rice or maize. The dynamics of CRWs and other retro...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1466688</comments>
            <pubDate>Thu, 22 May 2008 05:52:04 +0100</pubDate>
            <guid isPermaLink="false">1466688</guid>        </item>
        <item>
            <title>Intercalary heterochromatin in polytene chromosomes of 
 Drosophila melanogaster</title>
            <link>http://www.medworm.com/index.php?rid=1463148&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5p0u8p77k7466463%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Intercalary heterochromatin consists of extended chromosomal domains which are interspersed throughout the euchromatin and
 contain silent genetic material. These domains comprise either clusters of functionally unrelated genes or tandem gene duplications
 and possibly stretches of noncoding sequences. Strong repression of genetic activity means that intercalary heterochromatin
 displays properties that are normally attributable to classic pericentric heterochromatin: high compaction, late replication
 and underreplication in polytene chromosomes, and the presence of heterochromatin-specific proteins. Late replication and
 underreplication occurs when the suppressor of underreplication protein is present in intercalary heterochromatic regions.
 Intercalary heterochromat...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1463148</comments>
            <pubDate>Tue, 20 May 2008 06:16:43 +0100</pubDate>
            <guid isPermaLink="false">1463148</guid>        </item>
        <item>
            <title>Sites of strong Rec12/Spo11 binding in the fission yeast genome are associated with meiotic recombination and with centromeres</title>
            <link>http://www.medworm.com/index.php?rid=1417392&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb11t0m2010510765%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Meiotic recombination arises from Rec12/Spo11-dependent formation of DNA double-strand breaks (DSBs) and their subsequent
 repair. We identified Rec12-binding peaks across the Schizosaccharomyces pombe genome using chromatin immunoprecipitation after reversible formaldehyde cross-linking combined with whole-genome DNA microarrays.
 Strong Rec12 binding coincided with previously identified DSBs at the recombination hotspots ura4A, mbs1, and mbs2 and correlated with DSB formation at a new site. In addition, Rec12 binding corresponded to eight novel conversion hotspots
 and correlated with crossover density in segments of chromosome I. Notably, Rec12 binding inversely correlated with guanine–cytosine
 (GC) content, contrary to findings in Saccharomyces cerevisiae. Althou...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1417392</comments>
            <pubDate>Thu, 01 May 2008 06:28:09 +0100</pubDate>
            <guid isPermaLink="false">1417392</guid>        </item>
        <item>
            <title>Biogenesis of mRNPs: integrating different processes in the eukaryotic nucleus</title>
            <link>http://www.medworm.com/index.php?rid=1394739&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F56n51432v1984658%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Transcription is a central function occurring in the nucleus of eukaryotic cells in coordination with other nuclear processes.
 During transcription, the nascent pre-mRNA associates with mRNA-binding proteins and undergoes a series of processing steps,
 resulting in export-competent mRNA ribonucleoprotein complexes (mRNPs) that are transported into the cytoplasm. Experimental
 evidence increasingly indicates that the different processing steps (5′-end capping, splicing, 3′-end cleavage) and mRNP export
 are connected to each other as well as to transcription, both functionally and physically. Here, we review the overall process
 of mRNP biogenesis with particular emphasis on the functional coupling of transcription with mRNP biogenesis and export and
 its relationsh...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1394739</comments>
            <pubDate>Tue, 22 Apr 2008 13:59:44 +0100</pubDate>
            <guid isPermaLink="false">1394739</guid>        </item>
        <item>
            <title>The radial arrangement of the human chromosome 7 in the lymphocyte cell nucleus is associated with chromosomal band gene density</title>
            <link>http://www.medworm.com/index.php?rid=1383193&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F73262j802625544g%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In the nuclei of human lymphocytes, chromosome territories are distributed according to the average gene density of each chromosome.
 However, chromosomes are very heterogeneous in size and base composition, and can contain both very gene-dense and very gene-poor
 regions. Thus, a precise analysis of chromosome organisation in the nuclei should consider also the distribution of DNA belonging
 to the chromosomal bands in each chromosome. To improve our understanding of the chromatin organisation, we localised chromosome
 7 DNA regions, endowed with different gene densities, in the nuclei of human lymphocytes. Our results showed that this chromosome
 in cell nuclei is arranged radially with the gene-dense/GC-richest regions exposed towards the nuclear interior and the gen...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1383193</comments>
            <pubDate>Thu, 17 Apr 2008 15:14:40 +0100</pubDate>
            <guid isPermaLink="false">1383193</guid>        </item>
        <item>
            <title>Transcription-dependent spatial arrangements of CFTR and conserved adjacent loci are not conserved in human and murine nuclei</title>
            <link>http://www.medworm.com/index.php?rid=1371593&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff822383308617l23%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The human genes CFTR, ASZ1/GASZ, and CTTNBP2/CORTBP2 map to adjacent loci on chromosome 7q31 and display characteristic patterns
 of nuclear positioning, which strictly correlate with the state of activity. To address the evolutionary conservation of gene
 positioning, we investigated transcriptional activity and nuclear positioning of the highly conserved murine orthologs and
 of additional murine genes mapping to the region of conserved synteny on mouse chromosome 6. The results showed that all murine
 loci investigated constitutively localized in the nuclear interior irrespective of their functional state. Silenced loci did
 not display preferential association with the nuclear periphery or with chromocenters, respectively, and no differential positioning
 with respe...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1371593</comments>
            <pubDate>Sat, 12 Apr 2008 09:28:56 +0100</pubDate>
            <guid isPermaLink="false">1371593</guid>        </item>
        <item>
            <title>Production of diploid and triploid offspring by inbreeding of the triploid planarian 
 Dugesia ryukyuensis</title>
            <link>http://www.medworm.com/index.php?rid=1345855&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr23552508447873w%2F</link>
            <description>Content Type Journal ArticleCategory ErratumDOI 10.1007/s00412-008-0156-6Authors
		Kazuya Kobayashi, Keio University Department of Biosciences and Informatics Hiyoshi 3-14-1 Kouhoku-ku Yokohama 223-8522 JapanHirotsugu Ishizu, Keio University Department of Biosciences and Informatics Hiyoshi 3-14-1 Kouhoku-ku Yokohama 223-8522 JapanSachiko Arioka, Keio University Department of Biosciences and Informatics Hiyoshi 3-14-1 Kouhoku-ku Yokohama 223-8522 JapanJocelyn Padilla Cabrera, University of the Philippines Institute of Biology Diliman, Quezon City 1101 Manila PhilippinesMotonori Hoshi, Keio University Department of Biosciences and Informatics Hiyoshi 3-14-1 Kouhoku-ku Yokohama 223-8522 JapanMidori Matsumoto, Keio University Department of Biosciences and Informatics Hiyoshi 3-14-1 Kouhoku-...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1345855</comments>
            <pubDate>Tue, 01 Apr 2008 07:01:29 +0100</pubDate>
            <guid isPermaLink="false">1345855</guid>        </item>
        <item>
            <title>ZNF397, a new class of interphase to early prophase-specific, SCAN-zinc-finger, mammalian centromere protein</title>
            <link>http://www.medworm.com/index.php?rid=1336033&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft8697050602tp648%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The centromere is a complex structure required for equal segregation of newly synthesised sister chromatids at mitosis. One
 of the significant objectives in centromere research is to determine the complete repertoire of protein components that constitute
 the kinetochore. Here, we identify a novel centromere protein using a centromere-positive autoimmune serum from a patient
 with watermelon stomach disease. Western blot and screening of a lambda phage expression library revealed a 60-kDa protein,
 ZNF397. This protein belongs to the classical Cys2His2 group of the zinc-finger protein superfamily and contains two conserved domains: a leucine-rich SCAN domain and nine Cys2His2 zinc fingers. Bioinformatic analysis shows that ZNF397 is conserved in placental mammals. Stab...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1336033</comments>
            <pubDate>Fri, 28 Mar 2008 08:29:02 +0100</pubDate>
            <guid isPermaLink="false">1336033</guid>        </item>
        <item>
            <title>Recognition of DNA double strand breaks by the BRCA1 tumor suppressor network</title>
            <link>http://www.medworm.com/index.php?rid=1336034&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2x64162277544540%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;DNA double-strand breaks (DSBs) occur in response to both endogenous and exogenous genotoxic stress. Inappropriate repair
 of DSBs can lead to either loss of viability or to chromosomal alterations that increase the likelihood of cancer development.
 In strong support of this assertion, many cancer predisposition syndromes stem from germline mutations in genes involved in
 DNA DSB repair. Among the most prominent of such tumor suppressor genes are the Breast Cancer 1 and Breast Cancer 2 genes
 (BRCA1 and BRCA2), which are mutated in familial forms of breast and ovarian cancer. Recent findings implicate BRCA1 as a
 central component of several distinct macromolecular protein complexes, each dedicated to distinct elements of DNA DSB repair
 and tumor suppression. Emerging...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1336034</comments>
            <pubDate>Fri, 28 Mar 2008 08:29:01 +0100</pubDate>
            <guid isPermaLink="false">1336034</guid>        </item>
        <item>
            <title>Mre11 nuclease and C-terminal tail-mediated DDR functions are required for initiating yeast telomere healing</title>
            <link>http://www.medworm.com/index.php?rid=1301554&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj46230282038131h%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Mre11 is a central factor in creating an optimal substrate for telomerase loading and elongation. We have used a G2/M synchronized
 telomere-healing assay as a tool to separate different functions of Mre11 that are not apparent in null alleles. An analysis
 of healing efficiencies of several mre11 alleles revealed that both nuclease and C-terminal mutations led to a loss of healing. Interestingly, trans-complementation
 of the 49 amino acid C-terminal deletion (ΔC49) and the D16A mutant, deficient in nuclease activity and partially defective in MRX complex formation, restores healing. ΔC49 provokes
 Rad53 phosphorylation after treatment with the radiomimetic agent MMS exclusively through the Tel1 pathway, suggesting that
 a Tel1-mediated function is initiated through ...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1301554</comments>
            <pubDate>Wed, 12 Mar 2008 07:16:39 +0100</pubDate>
            <guid isPermaLink="false">1301554</guid>        </item>
        <item>
            <title>Integrated cytogenetic map of mitotic metaphase chromosome 9 of maize: resolution, sensitivity, and banding paint development</title>
            <link>http://www.medworm.com/index.php?rid=1281693&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6k541g3n8t161438%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To study the correlation of the sequence positions on the physical DNA finger print contig (FPC) map and cytogenetic maps
 of pachytene and somatic maize chromosomes, sequences located along the chromosome 9 FPC map approximately every 10&amp;nbsp;Mb were
 selected to place on maize chromosomes using fluorescent in situ hybridization (FISH). The probes were produced as pooled
 polymerase chain reaction products based on sequences of genetic markers or repeat-free portions of mapped bacterial artificial
 chromosome (BAC) clones. Fifteen probes were visualized on chromosome 9. The cytological positions of most sequences correspond
 on the pachytene, somatic, and FPC maps except some probes at the pericentromeric regions. Because of unequal condensation
 of mitotic metaphase c...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1281693</comments>
            <pubDate>Tue, 04 Mar 2008 08:45:15 +0100</pubDate>
            <guid isPermaLink="false">1281693</guid>        </item>
        <item>
            <title>Defining the role of Emi1 in the DNA replication–segregation cycle</title>
            <link>http://www.medworm.com/index.php?rid=1281694&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm467jr2283407777%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Ordered progression through the cell cycle is essential to maintain genomic stability, and fundamental to this is ubiquitin-mediated
 proteolysis. In particular, the anaphase-promoting complex/cyclosome (APC/C) ubiquitin ligase destabilises specific regulators
 at defined times in the cycle to ensure that each round of DNA replication is followed by cell division. Thus, the proper
 regulation of the APC/C is crucial in each cell cycle. There are several APC/C regulators that restrict its activity to specific
 cell cycle phases, and amongst these the early mitotic inhibitor 1 (Emi1) protein has recently come to prominence. Emi1 has
 been proposed to control APC/C in early mitosis; however, recent evidence questions this role. In this review we discuss new
 evidence that ...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1281694</comments>
            <pubDate>Tue, 04 Mar 2008 08:45:13 +0100</pubDate>
            <guid isPermaLink="false">1281694</guid>        </item>
        <item>
            <title>Cytological analysis of MRE11 protein during early meiotic prophase I in Arabidopsis and tomato</title>
            <link>http://www.medworm.com/index.php?rid=1257588&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq6721410m2124757%2F</link>
            <description>In this study, we describe the cytological
 behavior of a possible EN component, MRE11, a protein that is important for the repair of the numerous, programmed deoxyribonucleic
 acid double-strand breaks (DSBs) that occur early in the meiotic prophase. By immunofluorescence, many MRE11 foci were associated
 with chromosomal axes during early prophase I in both wild-type Arabidopsis and tomato primary microsporocytes. Similar patterns
 of MRE11 foci were observed in two Arabidopsis mutants (Atspo11-1 and Atprd1) that are defective in DSB formation and synapsis. In tomato chromosomes, MRE11 foci were more common in distal euchromatin
 than in proximal heterochromatin, consistent with known EN patterns. However, electron microscopic immunogold localization
 demonstrated that only about 10% of ...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1257588</comments>
            <pubDate>Fri, 22 Feb 2008 15:53:20 +0100</pubDate>
            <guid isPermaLink="false">1257588</guid>        </item>
        <item>
            <title>Evolutionary and clinical neocentromeres: two faces of the same coin?</title>
            <link>http://www.medworm.com/index.php?rid=1236681&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm278882441q51477%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;It has been hypothesized that human clinical neocentromeres and evolutionary novel centromeres (ENC) represent two faces of
 the same phenomenon. However, there are only two reports of loci harboring both a novel centromere and a clinical neocentromere.
 We suggest that only the tip of the iceberg has been scratched because most neocentromerization events have a very low chance
 of being observed. In support of this view, we report here on a neocentromere at 9q33.1 that emerged in a ring chromosome
 of about 12&amp;nbsp;Mb. The ring was produced by a balanced rearrangement that was fortuitously discovered because of its malsegregation
 in the propositus. Chromatin-immunoprecipitation-on-chip experiments using anti-centromere protein (CENP)-A and anti-CENP-C
 antibodies stro...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1236681</comments>
            <pubDate>Fri, 15 Feb 2008 18:03:25 +0100</pubDate>
            <guid isPermaLink="false">1236681</guid>        </item>
        <item>
            <title>Lim15/Dmc1 enhances DNA topoisomerase II catenation activity independent of sequence homology</title>
            <link>http://www.medworm.com/index.php?rid=1236682&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd728757039k6h532%2F</link>
            <description>In this study, the interaction between CcTopII and CcLim15, especially during catenation,
 was investigated in detail using atomic force microscopy. We demonstrated earlier that CcLim15 enhanced the catenation activity
 of CcTopII in a dose-dependent manner. When using two different-sized plasmid rings (5.4 and 3&amp;nbsp;kbp), which did not have any
 homologous sequence regions, equal proportions of homologous and heterologous catenanes were produced, suggesting that CcLim15
 causes an increase in catenation activity irrespective of the presence of homologous sequences between the rings. We also
 showed that CcLim15 works as a DNA-condensing agent. Therefore, we speculate that CcLim15 may work as a DNA-condensing factor
 specific to the zygotene event and that CcTopII is likely to resolve tan...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1236682</comments>
            <pubDate>Fri, 15 Feb 2008 18:03:24 +0100</pubDate>
            <guid isPermaLink="false">1236682</guid>        </item>
        <item>
            <title>Production of diploid and triploid offspring by inbreeding of the triploid planarian 
 Dugesia ryukyuensis</title>
            <link>http://www.medworm.com/index.php?rid=1192533&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8g03n77758745130%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Triploidy has generally been considered to be an evolutionary dead end due to problems of chromosomal pairing and segregation
 during meiosis. Thus, the formation of tetraploids and diploids from triploid types is a rare phenomenon. In the present study,
 we demonstrated that inbreeding of the triploid planarian Dugesia ryukyuensis resulted in both diploid and triploid offspring in nature. In the triploids of D. ryukyuensis, chiasmata between homologous chromosomes were observed in both female and male germ lines. This result suggests that both
 diploid and triploid offspring of this species are produced bisexually by zygotic fusion between sperm and eggs. Hence, this
 phenomenon may be a novel mechanism in planarian for escaping the triploid state.
 
	Content Type Jour...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1192533</comments>
            <pubDate>Tue, 29 Jan 2008 15:47:35 +0100</pubDate>
            <guid isPermaLink="false">1192533</guid>        </item>
        <item>
            <title>Size and number of tandem repeat arrays can determine somatic homologous pairing of transgene loci mediated by epigenetic modifications in 
 Arabidopsis thaliana
 nuclei</title>
            <link>http://www.medworm.com/index.php?rid=1160806&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F90v5p7256628p422%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The chromosomal arrangement of different transgenic repeat arrays inserted at various chromosomal positions was tested by
 FISH in Arabidopsis 2C leaf and root nuclei. Large lacO (∼10&amp;nbsp;kb) but not tetO (4.8&amp;nbsp;kb) or small lacO (∼2&amp;nbsp;kb) arrays were, in general, more often spatially associated with heterochromatic chromocenters (CC) than flanking regions
 (that either overlap the array insert position or are between 5 and 163&amp;nbsp;kb apart from the insert site). Allelic and ectopic
 pairing frequencies of lacO arrays were significantly increased only in nuclei of lines with two large lacO arrays inserted at different positions on the same chromosome arm. Within the same lines, root nuclei showed a significantly
 lower increase of pairing frequencies at the ...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1160806</comments>
            <pubDate>Thu, 17 Jan 2008 15:44:09 +0100</pubDate>
            <guid isPermaLink="false">1160806</guid>        </item>
        <item>
            <title>Global regulation of genome duplication in eukaryotes: an overview from the epifluorescence microscope</title>
            <link>http://www.medworm.com/index.php?rid=1157928&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1hg0458643486m12%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In eukaryotes, DNA replication is initiated along each chromosome at multiple sites called replication origins. Locally, each
 replication origin is “licensed” or specified at the end of the M and the beginning of the G1 phases of the cell cycle. During
 the S phase when DNA synthesis takes place, origins are activated in stages corresponding to early and late-replicating domains.
 The staged and progressive activation of replication origins reflects the need to maintain a strict balance between the number
 of active replication forks and the rate at which DNA synthesis proceeds. This suggests that origin densities (frequency of
 initiation) and replication fork movement (rates of elongation) must be coregulated to guarantee the efficient and complete
 duplication o...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1157928</comments>
            <pubDate>Wed, 16 Jan 2008 15:49:08 +0100</pubDate>
            <guid isPermaLink="false">1157928</guid>        </item>
        <item>
            <title>Telomere capping in Drosophila: dealing with chromosome ends that most resemble DNA breaks</title>
            <link>http://www.medworm.com/index.php?rid=1151970&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7wl3uw438g7226w3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Telomere caps prevent chromosome ends from being recognized as DNA double-strand breaks (DSBs). Unlike most organisms studied,
 the telomere-capping function of Drosophila does not require a specific sequence. Without this sequence component, Drosophila
 telomeres most resemble DNA breaks and, thus, represent a simpler system for the study of telomere capping. I review recent
 progress in Drosophila telomere studies, and challenge the notion that Drosophila may not be a relevant model for the study
 of telomere maintenance.
 
	Content Type Journal ArticleCategory ReviewDOI 10.1007/s00412-007-0144-2Authors
		Yikang S. Rong, National Institutes of Health Laboratory of Biochemistry and Molecular Biology, National Cancer Institute Bethesda Maryland 20892 USA
	

	
		Journal ...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1151970</comments>
            <pubDate>Mon, 14 Jan 2008 03:46:06 +0100</pubDate>
            <guid isPermaLink="false">1151970</guid>        </item>
        <item>
            <title>Arabidopsis
 sister chromatids often show complete alignment or separation along a 1.2-Mb euchromatic region but no cohesion “hot spots”</title>
            <link>http://www.medworm.com/index.php?rid=1149313&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F028086uw825520u3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Sister chromatid cohesion is a prerequisite for correct segregation and possibly other functions of replicated chromosomes.
 Except for yeast, no details are known about arrangement of cohesion sites along interphase chromosomes. Within nuclei of
 several higher plants, sister chromatids are frequently not aligned at various positions along chromosome arms. Therefore,
 we tested whether preferential alignment positions (“cohesion hot spots”) and constant extension of and distances between
 aligned sites occur in plants. Along a ~1.2-Mb contig from the bottom arm of chromosome 1, the sister chromatid positions
 of 13 individual BAC inserts were found to be aligned for ~67–77% of homologues in 4C Arabidopsis thaliana nuclei. The differences between the 13 BAC positi...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1149313</comments>
            <pubDate>Sat, 12 Jan 2008 16:33:29 +0100</pubDate>
            <guid isPermaLink="false">1149313</guid>        </item>
        <item>
            <title>RecQ helicases: guardian angels of the DNA replication fork</title>
            <link>http://www.medworm.com/index.php?rid=1145240&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F466151501425x762%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Since the original observations made in James German’s Laboratory that Bloom’s syndrome cells lacking BLM exhibit a decreased
 rate of both DNA chain elongation and maturation of replication intermediates, a large body of evidence has supported the
 idea that BLM, and other members of the RecQ helicase family to which BLM belongs, play important roles in DNA replication.
 More recent evidence indicates roles for RecQ helicases in what can broadly be defined as replication fork ‘repair’ processes
 when, for example, forks encounter lesions or adducts in the template, or when forks stall due to lack of nucleotide precursors.
 More specifically, several roles in repair of damaged forks via homologous recombination pathways have been proposed. RecQ
 helicases are ge...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1145240</comments>
            <pubDate>Fri, 11 Jan 2008 16:23:02 +0100</pubDate>
            <guid isPermaLink="false">1145240</guid>        </item>
        <item>
            <title>Dissection of a Y-autosome translocation in 
 Cryptomys hottentotus
 (Rodentia, Bathyergidae) and implications for the evolution of a meiotic sex chromosome chain</title>
            <link>http://www.medworm.com/index.php?rid=1111174&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F84476629656jx478%2F</link>
            <description>We describe the outcome of a comprehensive cytogenetic survey of the common mole-rat, Cryptomys hottentotus, based on G and C banding, fluorescence in situ hybridisation and the analysis of meiotic chromosomes using immunostaining
 of proteins involved in the formation of synaptonemal complex (SCP1 and SCP3). We identified the presence of a Y-autosome
 translocation that is responsible for a fixed diploid number difference between males (2n = 53) and females (2n = 54), a character that likely defines the C. hottentotus lineage. Immunostaining, combined with C banding of spermatocytes, revealed a linearised sex trivalent with X1 at one end and X2 at the other, with evidence of reduced recombination between Y and X2 that seems to be heterochromatin dependant in the C. hottentotus lin...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1111174</comments>
            <pubDate>Thu, 20 Dec 2007 16:24:14 +0100</pubDate>
            <guid isPermaLink="false">1111174</guid>        </item>
        <item>
            <title>The Suv39h–HP1 histone methylation pathway is dispensable for enrichment and protection of cohesin at centromeres in mammalian cells</title>
            <link>http://www.medworm.com/index.php?rid=1096966&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fhh6060738252877m%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Sister chromatids are physically connected by cohesin complexes. This sister chromatid cohesion is essential for the biorientation
 of chromosomes on the mitotic and meiotic spindle. In many species, cohesion between chromosome arms is partly dissolved in
 prophase of mitosis, whereas cohesion is protected at centromeres until the onset of anaphase. In vertebrates, the protein
 Sgo1, protein phosphatase 2A, and several other proteins are required for protection of centromeric cohesin in early mitosis.
 In fission yeast, the recruitment of heterochromatin protein Swi6/HP1 to centromeres by the histone-methyltransferase Clr4/Suv39h
 is required for enrichment of cohesin at centromeres already in interphase. We have tested if the Suv39h–HP1 histone methylation
 pathway i...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1096966</comments>
            <pubDate>Thu, 13 Dec 2007 17:20:39 +0100</pubDate>
            <guid isPermaLink="false">1096966</guid>        </item>
        <item>
            <title>Molecular and cytogenetic evidence for an allotetraploid origin of 
 Trifolium dubium
 (Leguminosae)</title>
            <link>http://www.medworm.com/index.php?rid=1079234&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2534162351360860%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Suckling clover, Trifolium dubium Sibth., is a European grassland legume that has spread to many parts of the world. The present work shows that it is an allotetraploid
 (2n = 4x = 30) combining the genomes of T. campestre Schreb. (2n = 2x = 14) and T. micranthum Viv. (2n = 2x = 16), two diploid species of similar geographic distribution. T. dubium has two nuclear ITS sequences that closely match those of T. campestre and T. micranthum. Genomic in situ hybridisation using genomic DNA of T. campestre and T. micranthum as probes has differentiated the ancestral sets of chromosomes in T. dubium cells. Comparative fluorescence in situ hybridisation analyses of 5S and 18S-26S rDNA loci were also consistent with an allotetraploid
 structure of the T. d...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1079234</comments>
            <pubDate>Thu, 06 Dec 2007 16:20:06 +0100</pubDate>
            <guid isPermaLink="false">1079234</guid>        </item>
        <item>
            <title>Multiple mechanisms of chromosome movement in vertebrate cells mediated through the Ndc80 complex and dynein/dynactin</title>
            <link>http://www.medworm.com/index.php?rid=1074235&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F035w3185l36772r3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Kinetochores bind microtubules laterally in a transient fashion and stably, by insertion of plus ends. These pathways may
 exist to carry out distinct tasks during different stages of mitosis and likely depend on distinct molecular mechanisms. On
 isolated chromosomes, we found microtubule nucleation/binding depended additively on both dynein/dynactin and on the Ndc80/Hec1
 complex. Studying chromosome movement in living Xenopus cells within the simplified geometry of monopolar spindles, we quantified the relative contributions of dynein/dynactin and
 the Ndc80/Hec1 complex. Inhibition of dynein/dynactin alone had minor effects but did suppress transient, rapid, poleward
 movements. In contrast, inhibition of the Ndc80 complex blocked normal end-on attachments of microt...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1074235</comments>
            <pubDate>Wed, 05 Dec 2007 16:36:37 +0100</pubDate>
            <guid isPermaLink="false">1074235</guid>        </item>
        <item>
            <title>Beyond the code: the mechanical properties of DNA as they relate to mitosis</title>
            <link>http://www.medworm.com/index.php?rid=1074236&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbk13014103hhuv11%2F</link>
            <description>Content Type Journal ArticleCategory Mini-ReviewDOI 10.1007/s00412-007-0138-0Authors
		Kerry S. Bloom, University of North Carolina at Chapel Hill Department of Biology 623 Fordham Hall CB#3280 Chapel Hill NC 27599–3280 USA
	

	
		Journal ChromosomaOnline ISSN 1432-0886Print ISSN 0009-5915 (Source: Chromosoma)</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1074236</comments>
            <pubDate>Mon, 03 Dec 2007 18:16:09 +0100</pubDate>
            <guid isPermaLink="false">1074236</guid>        </item>
        <item>
            <title>Fluorescence in situ hybridization (FISH) on maize metaphase chromosomes with quantum dot-labeled DNA conjugates</title>
            <link>http://www.medworm.com/index.php?rid=1062309&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw761805326r22w52%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Semiconductor nanocrystals, also called quantum dots (QDs), are novel inorganic fluorophores which are brighter and more photostable
 than organic fluorophores. In the present study, highly dispersive QD-labeled oligonucleotide (TAG)8 (QD-deoxyribonucleic acid [DNA]) conjugates were constructed via the metal-thiol bond, which can be used as fluorescence
 in situ hybridization (FISH) probes. FISH analysis of maize metaphase chromosomes using the QD-DNA probes showed that the
 probes could penetrate maize chromosomes and nuclei and solely hybridized to complementary target DNAs. Compared with the
 conventional organic dyes such as Cy3 and fluorescein isothiocyanate, this class of luminescent labels bound with oligonucleotides
 is brighter and more stable against photoblea...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1062309</comments>
            <pubDate>Thu, 29 Nov 2007 16:39:00 +0100</pubDate>
            <guid isPermaLink="false">1062309</guid>        </item>
        <item>
            <title>In vivo modeling of polysumoylation uncovers targeting of Topoisomerase II to the nucleolus via optimal level of SUMO modification</title>
            <link>http://www.medworm.com/index.php?rid=1062308&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm7t6k27p2211625k%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Conjugation of SUMO to target proteins is an essential eukaryotic regulatory pathway. Multiple potential SUMO substrates were
 identified among nuclear and chromatin proteins by proteomic approaches. However, the functional roles of SUMO-modified pools
 of individual proteins remain largely obscure, as only a small fraction of a given target is sumoylated and therefore is experimentally
 inaccessible. To overcome this technical difficulty in case of Topoisomerase II, we employed constitutive SUMO modification,
 enabling tracking of modified Top2p, not only biochemically but also cytologically and genetically. Topoisomerase II fused
 to a critical number of SUMO repeats is concentrated at the specific intranuclear domain, the nucleolus, when more than four
 SUMO moieties...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1062308</comments>
            <pubDate>Thu, 29 Nov 2007 16:39:00 +0100</pubDate>
            <guid isPermaLink="false">1062308</guid>        </item>
        <item>
            <title>Sodium arsenite modulates histone acetylation, histone deacetylase activity and HMGN protein dynamics in human cells</title>
            <link>http://www.medworm.com/index.php?rid=1026671&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg801m7834672q42g%2F</link>
            <description>In this study,
 we investigated the effects of sodium arsenite (NaAsO2) on global histone modifications and nucleosome-associated proteins. Our findings revealed that NaAsO2 exposure significantly increases global histone acetylation. This effect was related to the inhibition of histone deacetylase
 (HDAC) activity because NaAsO2 was able to inhibit HDACs comparable to the well-known HDAC inhibitor trichostatin A (TSA). Furthermore, analyses of the
 dynamic properties of the nucleosome-associated high mobility group N proteins demonstrate that NaAsO2 elevates their mobility. Thus, our data suggest that NaAsO2 induces chromatin opening by histone hyperacetylation due to HDAC inhibition and increase of the mobility of nucleosome-associated
 proteins. As the chromatin compaction is crucial fo...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1026671</comments>
            <pubDate>Tue, 13 Nov 2007 16:12:08 +0100</pubDate>
            <guid isPermaLink="false">1026671</guid>        </item>
        <item>
            <title>Drosophila gypsy
 insulator and 
 yellow
 enhancers regulate activity of 
 yellow
 promoter through the same regulatory element</title>
            <link>http://www.medworm.com/index.php?rid=1023991&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd521r472p4293x7w%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;There is ample evidence that the enhancers of a promoterless yellow locus in one homologous chromosome can activate the yellow promoter in the other chromosome where the enhancers are inactive or deleted, which is indicative of a high specificity of
 the enhancer–promoter interaction in yellow. In this paper, we have found that the yellow sequence from −100 to −69 is essential for stimulation of the heterologous eve (TATA-containing) and white (TATA-less) promoters by the yellow enhancers from a distance. However, the presence of this sequence is not required when the yellow enhancers are directly fused to the heterologous promoters or are activated by the yeast GAL4 activator. Unexpectedly, the
 same promoter proximal region defines previously described promoter-...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1023991</comments>
            <pubDate>Mon, 12 Nov 2007 08:21:43 +0100</pubDate>
            <guid isPermaLink="false">1023991</guid>        </item>
        <item>
            <title>Persistence of DNA threads in human anaphase cells suggests late completion of sister chromatid decatenation</title>
            <link>http://www.medworm.com/index.php?rid=1016844&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc62417414881l3j3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;PICH (Plk1-interacting checkpoint helicase) was recently identified as an essential component of the spindle assembly checkpoint
 and shown to localize to kinetochores, inner centromeres, and thin threads connecting separating chromosomes even during anaphase.
 In this paper, we have used immuno-fiber fluorescence in situ hybridization and chromatin-immunoprecipitation to demonstrate
 that PICH associates with centromeric chromatin during anaphase. Furthermore, by careful analysis of PICH-positive anaphase
 threads through FISH as well as bromo-deoxyurdine and CREST labeling, we strengthen the evidence that these threads comprise
 mainly alphoid centromere deoxyribonucleic acid. Finally, by timing the addition of ICRF-193 (a specific inhibitor of topoisomerase-II
 alpha...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1016844</comments>
            <pubDate>Thu, 08 Nov 2007 16:08:36 +0100</pubDate>
            <guid isPermaLink="false">1016844</guid>        </item>
        <item>
            <title>Molecular cloning of zebra finch W chromosome repetitive sequences: evolution of the avian W chromosome</title>
            <link>http://www.medworm.com/index.php?rid=998166&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ftp35qx98835u4070%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The zebra finch (Taeniopygia guttata) has a large Z chromosome and highly condensed W chromosome. We used the random amplified polymorphic DNA (RAPD) polymerase
 chain reaction (PCR) technique to isolate female-specific sequences ZBM1 and ZBM2. Southern blot hybridization to male and
 female zebra finch genomic DNA suggested that these sequences were located on the W chromosome, although homologous sequences
 appeared to be autosomal or Z-linked. Fluorescent in situ hybridization (FISH) using bacterial artificial chromosome (BAC)
 clones corresponding to ZBM sequences showed hybridization to the whole W chromosome, suggesting that the BACs encode sequences
 that are repeated across the entire W chromosome. Based on the sequencing of a ZBM repetitive sequence and Z chrom...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=998166</comments>
            <pubDate>Wed, 31 Oct 2007 14:45:11 +0100</pubDate>
            <guid isPermaLink="false">998166</guid>        </item>
        <item>
            <title>Differential distribution and association of repeat DNA sequences in the lateral element of the synaptonemal complex in rat spermatocytes</title>
            <link>http://www.medworm.com/index.php?rid=994492&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu436750938451h8n%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The synaptonemal complex (SC) is an evolutionarily conserved structure that mediates synapsis of homologous chromosomes during
 meiotic prophase I. Previous studies have established that the chromatin of homologous chromosomes is organized in loops that
 are attached to the lateral elements (LEs) of the SC. The characterization of the genomic sequences associated with LEs of
 the SC represents an important step toward understanding meiotic chromosome organization and function. To isolate these genomic
 sequences, we performed chromatin immunoprecipitation assays in rat spermatocytes using an antibody against SYCP3, a major
 structural component of the LEs of the SC. Our results demonstrated the reproducible and exclusive isolation of repeat deoxyribonucleic
 acid (DNA) ...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=994492</comments>
            <pubDate>Tue, 30 Oct 2007 14:43:26 +0100</pubDate>
            <guid isPermaLink="false">994492</guid>        </item>
        <item>
            <title>Association of cohesin and Nipped-B with transcriptionally active regions of the 
 Drosophila melanogaster
 genome</title>
            <link>http://www.medworm.com/index.php?rid=991256&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh15264x52223316n%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The cohesin complex is a chromosomal component required for sister chromatid cohesion that is conserved from yeast to man.
 The similarly conserved Nipped-B protein is needed for cohesin to bind to chromosomes. In higher organisms, Nipped-B and cohesin
 regulate gene expression and development by unknown mechanisms. Using chromatin immunoprecipitation, we find that Nipped-B
 and cohesin bind to the same sites throughout the entire non-repetitive Drosophila genome. They preferentially bind transcribed regions and overlap with RNA polymerase II. This contrasts sharply with yeast,
 where cohesin binds almost exclusively between genes. Differences in cohesin and Nipped-B binding between Drosophila cell lines often correlate with differences in gene expression. For example, ...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=991256</comments>
            <pubDate>Sat, 27 Oct 2007 17:34:31 +0100</pubDate>
            <guid isPermaLink="false">991256</guid>        </item>
        <item>
            <title>Inositol polyphosphates: a new frontier for regulating gene expression</title>
            <link>http://www.medworm.com/index.php?rid=963927&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm2774h6246200405%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Highly phosphorylated, soluble inositides are an emerging family of potential eukaryotic second messengers. The mechanisms
 for generating an outstanding diversity of mono- and pyrophosphorylated inositides have been recently elucidated and require
 a series of conserved lipases, kinases, and phosphatases. With several of the inositol kinases and the phospholipase C having
 access to the nucleus, roles for inositides in nuclear functions have been suggested. In support of this hypothesis, multiple
 studies have revealed the protein machines that are modulated by these inositides and found specific roles in nuclear physiology.
 In this paper, we review a novel paradigm for regulating gene expression at distinct steps by different inositide isomers.
 We discuss discoverie...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=963927</comments>
            <pubDate>Thu, 18 Oct 2007 16:14:58 +0100</pubDate>
            <guid isPermaLink="false">963927</guid>        </item>
        <item>
            <title>Topological constraints on the possible structures of the 30 nm chromatin fibre</title>
            <link>http://www.medworm.com/index.php?rid=955711&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F47tk591g125t6vt6%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The packing of mammalian DNA into chromatin plays an important role in cell differentiation and selection of epigenetically
 marked genes for expression or silencing. The first level of folding, the nucleosome, is evolutionary conserved. It allows
 transcription, after remodeling and/or histone modifications. The second level, the transcriptionally dormant 30&amp;nbsp;nm fibre,
 exhibits species and tissue variations in the chromatin repeat length. Nevertheless, very similar structures of fibres have
 been observed in all metazoans, and therefore, have to accommodate variable linker lengths with a corresponding change of
 tilt of the nucleosomes, which is defined by the DNA helical periodicity. So far, none of the models for a regular fibre structure
 has considered this re...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=955711</comments>
            <pubDate>Sat, 13 Oct 2007 17:13:33 +0100</pubDate>
            <guid isPermaLink="false">955711</guid>        </item>
        <item>
            <title>Functional links between 
 Drosophila
 Nipped-B and cohesin in somatic and meiotic cells</title>
            <link>http://www.medworm.com/index.php?rid=930047&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F63861x622n152315%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Drosophila Nipped-B is an essential protein that has multiple functions. It facilitates expression of homeobox genes and is also required
 for sister chromatid cohesion. Nipped-B is conserved from yeast to man, and its orthologs also play roles in deoxyribonucleic
 acid repair and meiosis. Mutation of the human ortholog, Nipped-B-Like (NIPBL), causes Cornelia de Lange syndrome (CdLS),
 associated with multiple developmental defects. The Nipped-B protein family is required for the cohesin complex that mediates
 sister chromatid cohesion to bind to chromosomes. A key question, therefore, is whether the Nipped-B family regulates gene
 expression, meiosis, and development by controlling cohesin. To gain insights into Nipped-B’s functions, we compared the effects
 of sev...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=930047</comments>
            <pubDate>Tue, 02 Oct 2007 16:12:59 +0100</pubDate>
            <guid isPermaLink="false">930047</guid>        </item>
        <item>
            <title>Long-distance interactions between regulatory elements are suppressed at the end of a terminally deficient chromosome in 
 Drosophila melanogaster</title>
            <link>http://www.medworm.com/index.php?rid=887669&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk3446632957r8446%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In Drosophila melanogaster, broken chromosome ends behave as real telomeres and are believed to be covered with telomere-specific chromatin. It has
 been shown previously that the telomeric chromatin represses normal activity of enhancers that regulate yellow expression in wings and body cuticle. In this paper, we have found that a modified yellow promoter is fully active in the wing and body cuticle when it is located at the chromosome end, which is evidence that the
 telomeric chromatin does not repress transcription. Substitution of the yellow core promoter region, including TATA and Inr, with the promoter regions of the eve, hsp70 (TATA-containing), and white (TATA-less) promoters does not affect the ability of the promoter to be cis- or trans-activated by the yello...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=887669</comments>
            <pubDate>Tue, 18 Sep 2007 19:38:40 +0100</pubDate>
            <guid isPermaLink="false">887669</guid>        </item>
        <item>
            <title>The trithorax group and Pc group proteins are differentially involved in heterochromatin formation in 
 Drosophila</title>
            <link>http://www.medworm.com/index.php?rid=852884&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc03p41x377888568%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In Drosophila, the Polycomb group and trithorax group proteins play a critical role in controlling the expression states of homeotic gene
 complexes during development. The common view is that these two classes of proteins bind to the homeotic complexes and regulate
 transcription at the level of chromatin. In the present work, we tested the involvement of both groups in mitotic heterochromatin
 formation in Drosophila. Using specific antibodies, we show that some of the tested Pc-G proteins are present in heterochromatin, while all the tested
 trx-G proteins localize to specific regions of heterochromatin in both mitotic chromosomes and interphase nuclei. We also
 observed that mutations in trx-G genes are recessive enhancers of position-effect variegation and are able...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=852884</comments>
            <pubDate>Fri, 07 Sep 2007 21:50:03 +0100</pubDate>
            <guid isPermaLink="false">852884</guid>        </item>
        <item>
            <title>Loading time of the centromeric histone H3 variant differs between plants and animals</title>
            <link>http://www.medworm.com/index.php?rid=845416&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2112k5660q44v537%2F</link>
            <description>Content TypeJournal Article

	
		JournalChromosomaOnline ISSN 1432-0886Print ISSN 0009-5915 (Source: Chromosoma)</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=845416</comments>
            <pubDate>Wed, 05 Sep 2007 07:04:45 +0100</pubDate>
            <guid isPermaLink="false">845416</guid>        </item>
        <item>
            <title>Displacement and re-accumulation of centromeric cohesin during transient pre-anaphase centromere splitting</title>
            <link>http://www.medworm.com/index.php?rid=841369&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx3t2411860289464%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The ring-shaped cohesin complex links sister chromatids until their timely segregation during mitosis. Cohesin is enriched
 at centromeres where it provides the cohesive counterforce to bipolar tension produced by the mitotic spindle. As a consequence
 of spindle tension, centromeric sequences transiently split in pre-anaphase cells, in some organisms up to several micrometers.
 This ‘centromere breathing’ presents a paradox, how sister sequences separate where cohesin is most enriched. We now show
 that in the budding yeast Saccharomyces cerevisiae, cohesin binding diminishes over centromeric sequences that split during breathing. We see no evidence for cohesin translocation
 to surrounding sequences, suggesting that cohesin is removed from centromeres during breat...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=841369</comments>
            <pubDate>Tue, 04 Sep 2007 14:48:45 +0100</pubDate>
            <guid isPermaLink="false">841369</guid>        </item>
        <item>
            <title>Two X family DNA polymerases, λ and μ, in meiotic tissues of the basidiomycete, 
 Coprinus cinereus</title>
            <link>http://www.medworm.com/index.php?rid=841368&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn2538q7m7185n277%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The X family DNA polymerases λ (CcPolλ) and μ (CcPolμ) were shown to be expressed during meiotic prophase in the basidiomycete, Coprinus cinereus. These two polymerases are the only members of the X family in the C. cinereus genome. The open reading frame of CcPolλ encoded a predicted product of 800 amino acid residues and that of CcPolμ of 621 amino acid residues. Both CcPolλ and CcPolμ required Mn2+ ions for activity, and both were strongly inhibited by dideoxythymidine triphosphate. Unlike their mammalian counterparts,
 CcPolλ and CcPolμ had no terminal deoxynucleotidyl transferase activity. Immunostaining analysis revealed that CcPolλ was
 present at meiotic prophase nuclei in zygotene and pachytene cells, which is the period when homologous chromosomes p...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=841368</comments>
            <pubDate>Tue, 04 Sep 2007 14:48:45 +0100</pubDate>
            <guid isPermaLink="false">841368</guid>        </item>
        <item>
            <title>Triplex configuration in the nick-free DNAs that constitute the chromosomal scaffolds in grasshopper spermatids</title>
            <link>http://www.medworm.com/index.php?rid=841367&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Feuh7462700181vx1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;After applying proper deoxyribonucleic acid (DNA) probes, fluorescence in situ hybridization (FISH) showed that the 8/9 centromeres—one
 per chromatid of the male haploid complement (X0) of Pyrgomorpha conica grasshopper—colocalized at the spermatid blunt end, where the spermatozoa flagellum inserts. A bundle of aligned 4′,6-diamidino-2-phenylindole-positive
 chromatid scaffolds, which formed the central spermatid core, was observed after DNA breakage detection followed by FISH.
 Modular nature of scaffold DNA was occasionally evident. The technique also showed that in the early spermatid, the chromatid
 scaffolds lacked any DNA nick, whereas abundant breaks accumulated in the surrounding loops. Moreover, immunodetection showed
 that scaffold DNA participated in t...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=841367</comments>
            <pubDate>Tue, 04 Sep 2007 14:48:45 +0100</pubDate>
            <guid isPermaLink="false">841367</guid>        </item>
        <item>
            <title>Microtubule breakage is not a major mechanism for resolving end-to-end chromosome fusions generated by telomere dysfunction during the early process of immortalization</title>
            <link>http://www.medworm.com/index.php?rid=830686&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Frm382h77q70w3nw2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Telomeres, the terminal chromosomal structure crucial for maintaining genomic integrity, shorten with deoxyribonucleic acid
 replications in most human somatic cells. Chromosomes carrying critically short telomeres tend to form end-to-end fusions,
 which are subject to breakage during cell division. However, it remains obscure how such telomere-mediated fusions are resolved
 during the process of immortalization, which is an early and indispensable step toward cancer. It has been hypothesized that
 the breakage could occur at either the microtubule or chromatid, causing numerical or structural chromosome instability, respectively.
 In this paper, we show that although the distributions of chromosomal segment losses or gains involved in structural aberrations
 were signi...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=830686</comments>
            <pubDate>Wed, 29 Aug 2007 07:03:56 +0100</pubDate>
            <guid isPermaLink="false">830686</guid>        </item>
        <item>
            <title>Another way to move chromosomes</title>
            <link>http://www.medworm.com/index.php?rid=744390&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fet8112481h3ug3h8%2F</link>
            <description>In this study, we highlight another way of moving chromosomes remotely from outside the nucleus, which
 involves SUN and KASH domain nuclear envelope proteins. SUN and KASH domain protein families are known to connect the nucleus
 to cytoskeletal networks and play a role in migration and positioning of the nucleus. Recent studies in the fission yeast
 Schizossacharomyces pombe demonstrated an additional role for the SUN–KASH protein complex in chromosome movements. During meiotic prophase, telomeres
 are moved to rearrange chromosomes within the nucleus. The SUN–KASH protein complex located in the nuclear envelope is involved
 in this process. Telomeres are connected to the SUN protein on the nucleoplasmic side, and the dynein motor complex binds
 to the KASH protein on the cytoplasmic...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=744390</comments>
            <pubDate>Wed, 18 Jul 2007 06:47:36 +0100</pubDate>
            <guid isPermaLink="false">744390</guid>        </item>
        <item>
            <title>Tandem 41-bp repeats in chicken and Japanese quail genomes: FISH mapping and transcription analysis on lampbrush chromosomes</title>
            <link>http://www.medworm.com/index.php?rid=729468&amp;cid=s_33449_176_f&amp;fid=33449&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg6n915472n474m2w%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The chromosomal distribution of 41-bp repeats, known as CNM and PO41 repeats in the chicken genome and BglII repeats in the Japanese quail, was analyzed precisely using giant lampbrush chromosomes (LBC) from chicken, Japanese quail,
 and turkey growing oocytes. The PO41 repeat is conserved in all galliform species, whereas the other repeats are species specific.
 In chicken and quail, the centromere and subtelomere regions share homologous satellite sequences. RNA polymerase II transcribes
 the 41-bp repeats in both centromere and subtelomere regions. Ongoing transcription of these repeats was demonstrated by incorporation
 of BrUTP injected into oocytes at the lampbrush stage. RNA complementary to both strands of CNM and PO41 repeats is present
 on chicken LBC loops, w...</description>
            <author>Chromosoma</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=729468</comments>
            <pubDate>Tue, 10 Jul 2007 07:18:41 +0100</pubDate>
            <guid isPermaLink="false">729468</guid>        </item>
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