<?xml version="1.0" encoding="UTF-8"?>
<mx:collection xmlns:mx="http://www.loc.gov/MARC21/slim">
    <mx:record id="11518">
        <mx:leader/>
        <datafield tag="022" ind1="" ind2="">
            <subfield code="a">1559-2294</subfield>
        </datafield>
        <datafield tag="100" ind1="" ind2="">
            <subfield code="a">Akiko  Inagaki</subfield>
            <subfield code="a">Sam  Schoenmakers and Willy M. Baarends</subfield>
        </datafield>
        
        <datafield tag="210" ind1="" ind2="">
            <subfield code="a">epigenetics</subfield>
        </datafield>
        
        <datafield tag="245" ind1="" ind2="">
            <subfield code="a">DNA double strand break repair, chromosome synapsis and transcriptional silencing in meiosis</subfield> 
        </datafield>
        
        <datafield tag="260" ind1="3" ind2="">
            <subfield code="b">Landes Bioscience</subfield>
            <subfield code="c">2010-05-16</subfield>
        </datafield>
        
        <datafield tag="302" ind1="" ind2="">
            <subfield code="a">255 - 266</subfield>
        </datafield>
        
        <datafield tag="440" ind1="" ind2="">
            
            <subfield code="a">Epigenetics</subfield>
            <subfield code="v">5-4</subfield>
        </datafield>
        <datafield tag="449" ind1="" ind2="">
            <subfield code="o">Landes Bioscience</subfield>
        </datafield>
        <datafield tag="520" ind1="3" ind2="">
            <subfield code="a">Chromosome pairing and synapsis during meiotic prophase requires the formation and repair of DNA double-strand breaks (DSBs) by the topoisomerase-like enzyme SPO11. Chromosomes, or chromosomal regions, that lack a pairing partner, such as the largely heterologous X and Y chromosomes, show delayed meiotic DSB repair and are transcriptionally silenced. Herein, we review meiosis-specific aspects of DSB repair in relation to homology recognition and meiotic silencing of heterologous regions. We propose a dynamic interplay between progression of synapsis and persistent meiotic DSBs. Signaling from these persistent breaks could inhibit heterologous synapsis and stimulate meiotic silencing of the X and Y chromosomes.</subfield>
        </datafield>
        <datafield tag="856" ind1="4" ind2="">
            
            <subfield code="u">http://dx.doi.org/10.4161/epi.5.4.11518</subfield>
            <subfield code="u">http://www.landesbioscience.com/journals/epigenetics/article/11518/</subfield>
        </datafield>
 
        <datafield tag="949" ind1="" ind2="">
            <subfield code="t">article</subfield>
            <subfield code="n">Point-of-View</subfield>
        </datafield>
    </mx:record>

</mx:collection>