Shifts in Replication Timing Actively Affect Histone Acetylation during Nucleosome Reassembly
The entire genome is replicated in a programmed manner, with specific regions undergoing DNA synthesis at different times in S phase. Active genes generally replicate in early S phase, while repressed genes replicate late, and for some loci this process is developmentally regulated. Using a nuclear...
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Veröffentlicht in: | Molecular cell 2009-06, Vol.34 (6), p.767-774 |
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description | The entire genome is replicated in a programmed manner, with specific regions undergoing DNA synthesis at different times in S phase. Active genes generally replicate in early S phase, while repressed genes replicate late, and for some loci this process is developmentally regulated. Using a nuclear microinjection system, we demonstrate that DNA sequences originally packaged into nucleosomes containing deacetylated histones during late S become reassembled with acetylated histones after undergoing replication in early S. Conversely, a change from early to late replication timing is accompanied by repackaging into nucleosomes containing deacetylated histones. This is carried out by differential cell-cycle-controlled acetylation and deacetylation of histones H3 and H4. These studies provide strong evidence that switches in replication timing may play a role in the regulation of nucleosome structure during development. |
doi_str_mv | 10.1016/j.molcel.2009.05.027 |
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Active genes generally replicate in early S phase, while repressed genes replicate late, and for some loci this process is developmentally regulated. Using a nuclear microinjection system, we demonstrate that DNA sequences originally packaged into nucleosomes containing deacetylated histones during late S become reassembled with acetylated histones after undergoing replication in early S. Conversely, a change from early to late replication timing is accompanied by repackaging into nucleosomes containing deacetylated histones. This is carried out by differential cell-cycle-controlled acetylation and deacetylation of histones H3 and H4. These studies provide strong evidence that switches in replication timing may play a role in the regulation of nucleosome structure during development.</description><identifier>ISSN: 1097-2765</identifier><identifier>EISSN: 1097-4164</identifier><identifier>DOI: 10.1016/j.molcel.2009.05.027</identifier><identifier>PMID: 19560427</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Acetylation ; Animals ; Cell Line ; CELLCYCLE ; DNA ; DNA Replication - physiology ; Histones - chemistry ; Histones - genetics ; Histones - metabolism ; Microinjections ; Models, Genetic ; Nucleosomes - chemistry ; Nucleosomes - genetics ; Nucleosomes - metabolism ; Protein Processing, Post-Translational ; Rats ; S Phase</subject><ispartof>Molecular cell, 2009-06, Vol.34 (6), p.767-774</ispartof><rights>2009 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c527t-3ab2c134380fd7b4310fd75220dae2119e488c5d8de14c463f6f0bbed9a6e36b3</citedby><cites>FETCH-LOGICAL-c527t-3ab2c134380fd7b4310fd75220dae2119e488c5d8de14c463f6f0bbed9a6e36b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.molcel.2009.05.027$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19560427$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lande-Diner, Laura</creatorcontrib><creatorcontrib>Zhang, Jianmin</creatorcontrib><creatorcontrib>Cedar, Howard</creatorcontrib><title>Shifts in Replication Timing Actively Affect Histone Acetylation during Nucleosome Reassembly</title><title>Molecular cell</title><addtitle>Mol Cell</addtitle><description>The entire genome is replicated in a programmed manner, with specific regions undergoing DNA synthesis at different times in S phase. Active genes generally replicate in early S phase, while repressed genes replicate late, and for some loci this process is developmentally regulated. Using a nuclear microinjection system, we demonstrate that DNA sequences originally packaged into nucleosomes containing deacetylated histones during late S become reassembled with acetylated histones after undergoing replication in early S. Conversely, a change from early to late replication timing is accompanied by repackaging into nucleosomes containing deacetylated histones. This is carried out by differential cell-cycle-controlled acetylation and deacetylation of histones H3 and H4. These studies provide strong evidence that switches in replication timing may play a role in the regulation of nucleosome structure during development.</description><subject>Acetylation</subject><subject>Animals</subject><subject>Cell Line</subject><subject>CELLCYCLE</subject><subject>DNA</subject><subject>DNA Replication - physiology</subject><subject>Histones - chemistry</subject><subject>Histones - genetics</subject><subject>Histones - metabolism</subject><subject>Microinjections</subject><subject>Models, Genetic</subject><subject>Nucleosomes - chemistry</subject><subject>Nucleosomes - genetics</subject><subject>Nucleosomes - metabolism</subject><subject>Protein Processing, Post-Translational</subject><subject>Rats</subject><subject>S Phase</subject><issn>1097-2765</issn><issn>1097-4164</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9v3CAQxVHVqPnTfoOq8qm3dQBjsC-VVlGbRIoSKUmPFcIw3rDCZgt4pf32wdpVN73kNAjevBneD6GvBJcEE365LgfvNLiSYtyWuC4xFR_QGcGtWDDC2cfDmQpen6LzGNcYE1Y37Sd0StqaY0bFGfrz9GL7FAs7Fo-wcVarZP1YPNvBjqtiqZPdgtsVy74HnYobG5MfId9D2rm91Exhlt5P2oGPfoBspGKEoXO7z-ikVy7Cl0O9QL9__Xy-ulncPVzfXi3vFrqmIi0q1VFNKlY1uDeiYxWZa00pNgooIS2wptG1aQwQphmvet7jrgPTKg4V76oL9GPvu5m6AYyGMQXl5CbYQYWd9MrK_19G-yJXfiupIEKwKht8PxgE_3eCmORgYw7XqRH8FCXPIkLELGR7oQ4-xgD9vyEEy5mLXMs9FzlzkbiWmUtu-_Z2wWPTAcTxB5Bj2loIMmoLowZjQ05eGm_fn_AKmcejlQ</recordid><startdate>20090626</startdate><enddate>20090626</enddate><creator>Lande-Diner, Laura</creator><creator>Zhang, Jianmin</creator><creator>Cedar, Howard</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20090626</creationdate><title>Shifts in Replication Timing Actively Affect Histone Acetylation during Nucleosome Reassembly</title><author>Lande-Diner, Laura ; Zhang, Jianmin ; Cedar, Howard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c527t-3ab2c134380fd7b4310fd75220dae2119e488c5d8de14c463f6f0bbed9a6e36b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Acetylation</topic><topic>Animals</topic><topic>Cell Line</topic><topic>CELLCYCLE</topic><topic>DNA</topic><topic>DNA Replication - physiology</topic><topic>Histones - chemistry</topic><topic>Histones - genetics</topic><topic>Histones - metabolism</topic><topic>Microinjections</topic><topic>Models, Genetic</topic><topic>Nucleosomes - chemistry</topic><topic>Nucleosomes - genetics</topic><topic>Nucleosomes - metabolism</topic><topic>Protein Processing, Post-Translational</topic><topic>Rats</topic><topic>S Phase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lande-Diner, Laura</creatorcontrib><creatorcontrib>Zhang, Jianmin</creatorcontrib><creatorcontrib>Cedar, Howard</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lande-Diner, Laura</au><au>Zhang, Jianmin</au><au>Cedar, Howard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Shifts in Replication Timing Actively Affect Histone Acetylation during Nucleosome Reassembly</atitle><jtitle>Molecular cell</jtitle><addtitle>Mol Cell</addtitle><date>2009-06-26</date><risdate>2009</risdate><volume>34</volume><issue>6</issue><spage>767</spage><epage>774</epage><pages>767-774</pages><issn>1097-2765</issn><eissn>1097-4164</eissn><abstract>The entire genome is replicated in a programmed manner, with specific regions undergoing DNA synthesis at different times in S phase. 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subjects | Acetylation Animals Cell Line CELLCYCLE DNA DNA Replication - physiology Histones - chemistry Histones - genetics Histones - metabolism Microinjections Models, Genetic Nucleosomes - chemistry Nucleosomes - genetics Nucleosomes - metabolism Protein Processing, Post-Translational Rats S Phase |
title | Shifts in Replication Timing Actively Affect Histone Acetylation during Nucleosome Reassembly |
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