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   	<dc:title>Dynamic regulation of histone modifications and long-range chromosomal interactions during postmitotic transcriptional reactivation</dc:title>
   	<dc:creator>Kang, Hyeseon</dc:creator>
   	<dc:creator>Shokhirev, Maxim N.</dc:creator>
   	<dc:creator>Xu, Zhichao</dc:creator>
   	<dc:creator>Chandran, Sahaana</dc:creator>
   	<dc:creator>Dixon, Jesse R.</dc:creator>
   	<dc:creator>HETZER, Martin W ; https://orcid.org/0000-0002-2111-992X</dc:creator>
   	<dc:subject>Developmental Biology</dc:subject>
   	<dc:subject>Genetics</dc:subject>
   	<dc:subject>ddc:570</dc:subject>
   	<dc:description>During mitosis, transcription of genomic DNA is dramatically reduced, before it is reactivated during nuclear reformation in anaphase/telophase. Many aspects of the underlying principles that mediate transcriptional memory and reactivation in the daughter cells remain unclear. Here, we used ChIP-seq on synchronized cells at different stages after mitosis to generate genome-wide maps of histone modifications. Combined with EU-RNA-seq and Hi-C analyses, we found that during prometaphase, promoters, enhancers, and insulators retain H3K4me3 and H3K4me1, while losing H3K27ac. Enhancers globally retaining mitotic H3K4me1 or locally retaining mitotic H3K27ac are associated with cell type-specific genes and their transcription factors for rapid transcriptional activation. As cells exit mitosis, promoters regain H3K27ac, which correlates with transcriptional reactivation. Insulators also gain H3K27ac and CCCTC-binding factor (CTCF) in anaphase/telophase. This increase of H3K27ac in anaphase/telophase is required for posttranscriptional activation and may play a role in the establishment of topologically associating domains (TADs). Together, our results suggest that the genome is reorganized in a sequential order, in which histone methylations occur first in prometaphase, histone acetylation, and CTCF in anaphase/telophase, transcription in cytokinesis, and long-range chromatin interactions in early G1. We thus provide insights into the histone modification landscape that allows faithful reestablishment of the transcriptional program and TADs during cell division.</dc:description>
   	<dc:publisher>Cold Spring Harbor Laboratory Press</dc:publisher>
   	<dc:date>2020</dc:date>
   	<dc:type>info:eu-repo/semantics/article</dc:type>
   	<dc:type>doc-type:article</dc:type>
   	<dc:type>text</dc:type>
   	<dc:type>http://purl.org/coar/resource_type/c_2df8fbb1</dc:type>
   	<dc:identifier>https://research-explorer.ista.ac.at/record/11057</dc:identifier>
   	<dc:identifier>https://research-explorer.ista.ac.at/download/11057/11136</dc:identifier>
   	<dc:source>Kang H, Shokhirev MN, Xu Z, Chandran S, Dixon JR, Hetzer M. Dynamic regulation of histone modifications and long-range chromosomal interactions during postmitotic transcriptional reactivation. &lt;i&gt;Genes &amp;#38; Development&lt;/i&gt;. 2020;34(13-14):913-930. doi:&lt;a href=&quot;https://doi.org/10.1101/gad.335794.119&quot;&gt;10.1101/gad.335794.119&lt;/a&gt;</dc:source>
   	<dc:language>eng</dc:language>
   	<dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1101/gad.335794.119</dc:relation>
   	<dc:relation>info:eu-repo/semantics/altIdentifier/issn/0890-9369</dc:relation>
   	<dc:relation>info:eu-repo/semantics/altIdentifier/issn/1549-5477</dc:relation>
   	<dc:relation>info:eu-repo/semantics/altIdentifier/pmid/32499403</dc:relation>
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