Multiple Structural Maintenance of Chromosome Complexes at Transcriptional Regulatory Elements
Transcription factors control cell-specific gene expression programs by binding regulatory elements and recruiting cofactors and the transcription apparatus to the initiation sites of active genes. One of these cofactors is cohesin, a structural maintenance of chromosomes (SMC) complex that is neces...
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Veröffentlicht in: | Stem cell reports 2013-11, Vol.1 (5), p.371-378 |
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description | Transcription factors control cell-specific gene expression programs by binding regulatory elements and recruiting cofactors and the transcription apparatus to the initiation sites of active genes. One of these cofactors is cohesin, a structural maintenance of chromosomes (SMC) complex that is necessary for proper gene expression. We report that a second SMC complex, condensin II, is also present at transcriptional regulatory elements of active genes during interphase and is necessary for normal gene activity. Both cohesin and condensin II are associated with genes in euchromatin and not heterochromatin. The two SMC complexes and the SMC loading factor NIPBL are particularly enriched at super-enhancers, and the genes associated with these regulatory elements are especially sensitive to reduced levels of these complexes. Thus, in addition to their well-established functions in chromosome maintenance during mitosis, both cohesin and condensin II make important contributions to the functions of the key transcriptional regulatory elements during interphase.
•Cohesin and condensin II occupancy of enhancers and promoters is NIPBL dependent•Condensin II is recruited to regulatory elements during transcription activation•Cohesin and condensin II occupy super-enhancers and mediate proper gene expression
The SMC complexes cohesin and condensin II occupy enhancers and promoters in a NIPBL-dependent manner. Condensin II is recruited to active regulatory elements during transcription activation in interphase cells. Both cohesin and condensin II occupy super-enhancers and are required for proper gene expression. |
doi_str_mv | 10.1016/j.stemcr.2013.09.002 |
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•Cohesin and condensin II occupancy of enhancers and promoters is NIPBL dependent•Condensin II is recruited to regulatory elements during transcription activation•Cohesin and condensin II occupy super-enhancers and mediate proper gene expression
The SMC complexes cohesin and condensin II occupy enhancers and promoters in a NIPBL-dependent manner. Condensin II is recruited to active regulatory elements during transcription activation in interphase cells. Both cohesin and condensin II occupy super-enhancers and are required for proper gene expression.</description><identifier>ISSN: 2213-6711</identifier><identifier>EISSN: 2213-6711</identifier><identifier>DOI: 10.1016/j.stemcr.2013.09.002</identifier><identifier>PMID: 24286025</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adenosine Triphosphatases - metabolism ; Animals ; Cell Cycle Proteins - metabolism ; Cell Line, Tumor ; Cells, Cultured ; Chromatin - metabolism ; Chromosomal Proteins, Non-Histone - metabolism ; Cohesins ; DNA-Binding Proteins - metabolism ; Embryonic Stem Cells - metabolism ; Enhancer Elements, Genetic ; Gene Expression Regulation, Developmental ; Humans ; Mice ; Mice, Inbred C57BL ; Multiprotein Complexes - metabolism ; Protein Binding ; Transcriptional Activation</subject><ispartof>Stem cell reports, 2013-11, Vol.1 (5), p.371-378</ispartof><rights>2013 The Authors</rights><rights>2013 The Authors 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c529t-29c2dff01d49851376685bc6f669e29478cd4ae32e021141ff7c8512a9aba57a3</citedby><cites>FETCH-LOGICAL-c529t-29c2dff01d49851376685bc6f669e29478cd4ae32e021141ff7c8512a9aba57a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841252/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841252/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24286025$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dowen, Jill M.</creatorcontrib><creatorcontrib>Bilodeau, Steve</creatorcontrib><creatorcontrib>Orlando, David A.</creatorcontrib><creatorcontrib>Hübner, Michael R.</creatorcontrib><creatorcontrib>Abraham, Brian J.</creatorcontrib><creatorcontrib>Spector, David L.</creatorcontrib><creatorcontrib>Young, Richard A.</creatorcontrib><title>Multiple Structural Maintenance of Chromosome Complexes at Transcriptional Regulatory Elements</title><title>Stem cell reports</title><addtitle>Stem Cell Reports</addtitle><description>Transcription factors control cell-specific gene expression programs by binding regulatory elements and recruiting cofactors and the transcription apparatus to the initiation sites of active genes. One of these cofactors is cohesin, a structural maintenance of chromosomes (SMC) complex that is necessary for proper gene expression. We report that a second SMC complex, condensin II, is also present at transcriptional regulatory elements of active genes during interphase and is necessary for normal gene activity. Both cohesin and condensin II are associated with genes in euchromatin and not heterochromatin. The two SMC complexes and the SMC loading factor NIPBL are particularly enriched at super-enhancers, and the genes associated with these regulatory elements are especially sensitive to reduced levels of these complexes. Thus, in addition to their well-established functions in chromosome maintenance during mitosis, both cohesin and condensin II make important contributions to the functions of the key transcriptional regulatory elements during interphase.
•Cohesin and condensin II occupancy of enhancers and promoters is NIPBL dependent•Condensin II is recruited to regulatory elements during transcription activation•Cohesin and condensin II occupy super-enhancers and mediate proper gene expression
The SMC complexes cohesin and condensin II occupy enhancers and promoters in a NIPBL-dependent manner. Condensin II is recruited to active regulatory elements during transcription activation in interphase cells. Both cohesin and condensin II occupy super-enhancers and are required for proper gene expression.</description><subject>Adenosine Triphosphatases - metabolism</subject><subject>Animals</subject><subject>Cell Cycle Proteins - metabolism</subject><subject>Cell Line, Tumor</subject><subject>Cells, Cultured</subject><subject>Chromatin - metabolism</subject><subject>Chromosomal Proteins, Non-Histone - metabolism</subject><subject>Cohesins</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Embryonic Stem Cells - metabolism</subject><subject>Enhancer Elements, Genetic</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Humans</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Multiprotein Complexes - metabolism</subject><subject>Protein Binding</subject><subject>Transcriptional Activation</subject><issn>2213-6711</issn><issn>2213-6711</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kctO3DAUhq0KBIjyBqjKsptJfU4cJ95UqkbQVgIhFdhieZwT8CiJB9tB5e1rNNy6wRtb8n_x8cfYMfASOMhv6zImGm0okUNVclVyjp_YASJUC9kA7Lw777OjGNc8L6UABeyxfRTYSo71Abs5n4fkNgMVlynMNs3BDMW5cVOiyUyWCt8Xy7vgRx_9SMXSj1n7l2JhUnEVzBRtcJvk_JRtf-h2Hkzy4bE4GWikKcXPbLc3Q6Sj5_2QXZ-eXC1_Lc4ufv5e_jhb2BpVWqCy2PU9h06otoaqkbKtV1b2UipCJZrWdsJQhcQRQEDfNzbr0CizMnVjqkP2fZu7mVcjdTZ350H0JrjRhEftjdP_30zuTt_6B121ArDGHPD1OSD4-5li0qOLlobBTOTnqEFIhbytWpmlYiu1wccYqH-tAa6f6Oi13tLRT3Q0VzrTybYv75_4anph8TYD5Y96cBR0tI4yg84Fskl33n3c8A8vdKUQ</recordid><startdate>20131119</startdate><enddate>20131119</enddate><creator>Dowen, Jill M.</creator><creator>Bilodeau, Steve</creator><creator>Orlando, David A.</creator><creator>Hübner, Michael R.</creator><creator>Abraham, Brian J.</creator><creator>Spector, David L.</creator><creator>Young, Richard A.</creator><general>Elsevier Inc</general><general>Elsevier</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>20131119</creationdate><title>Multiple Structural Maintenance of Chromosome Complexes at Transcriptional Regulatory Elements</title><author>Dowen, Jill M. ; Bilodeau, Steve ; Orlando, David A. ; Hübner, Michael R. ; Abraham, Brian J. ; Spector, David L. ; Young, Richard A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c529t-29c2dff01d49851376685bc6f669e29478cd4ae32e021141ff7c8512a9aba57a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adenosine Triphosphatases - metabolism</topic><topic>Animals</topic><topic>Cell Cycle Proteins - metabolism</topic><topic>Cell Line, Tumor</topic><topic>Cells, Cultured</topic><topic>Chromatin - metabolism</topic><topic>Chromosomal Proteins, Non-Histone - metabolism</topic><topic>Cohesins</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Embryonic Stem Cells - metabolism</topic><topic>Enhancer Elements, Genetic</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Humans</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Multiprotein Complexes - metabolism</topic><topic>Protein Binding</topic><topic>Transcriptional Activation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dowen, Jill M.</creatorcontrib><creatorcontrib>Bilodeau, Steve</creatorcontrib><creatorcontrib>Orlando, David A.</creatorcontrib><creatorcontrib>Hübner, Michael R.</creatorcontrib><creatorcontrib>Abraham, Brian J.</creatorcontrib><creatorcontrib>Spector, David L.</creatorcontrib><creatorcontrib>Young, Richard A.</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>Stem cell reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dowen, Jill M.</au><au>Bilodeau, Steve</au><au>Orlando, David A.</au><au>Hübner, Michael R.</au><au>Abraham, Brian J.</au><au>Spector, David L.</au><au>Young, Richard A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multiple Structural Maintenance of Chromosome Complexes at Transcriptional Regulatory Elements</atitle><jtitle>Stem cell reports</jtitle><addtitle>Stem Cell Reports</addtitle><date>2013-11-19</date><risdate>2013</risdate><volume>1</volume><issue>5</issue><spage>371</spage><epage>378</epage><pages>371-378</pages><issn>2213-6711</issn><eissn>2213-6711</eissn><abstract>Transcription factors control cell-specific gene expression programs by binding regulatory elements and recruiting cofactors and the transcription apparatus to the initiation sites of active genes. One of these cofactors is cohesin, a structural maintenance of chromosomes (SMC) complex that is necessary for proper gene expression. We report that a second SMC complex, condensin II, is also present at transcriptional regulatory elements of active genes during interphase and is necessary for normal gene activity. Both cohesin and condensin II are associated with genes in euchromatin and not heterochromatin. The two SMC complexes and the SMC loading factor NIPBL are particularly enriched at super-enhancers, and the genes associated with these regulatory elements are especially sensitive to reduced levels of these complexes. Thus, in addition to their well-established functions in chromosome maintenance during mitosis, both cohesin and condensin II make important contributions to the functions of the key transcriptional regulatory elements during interphase.
•Cohesin and condensin II occupancy of enhancers and promoters is NIPBL dependent•Condensin II is recruited to regulatory elements during transcription activation•Cohesin and condensin II occupy super-enhancers and mediate proper gene expression
The SMC complexes cohesin and condensin II occupy enhancers and promoters in a NIPBL-dependent manner. Condensin II is recruited to active regulatory elements during transcription activation in interphase cells. Both cohesin and condensin II occupy super-enhancers and are required for proper gene expression.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>24286025</pmid><doi>10.1016/j.stemcr.2013.09.002</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenosine Triphosphatases - metabolism Animals Cell Cycle Proteins - metabolism Cell Line, Tumor Cells, Cultured Chromatin - metabolism Chromosomal Proteins, Non-Histone - metabolism Cohesins DNA-Binding Proteins - metabolism Embryonic Stem Cells - metabolism Enhancer Elements, Genetic Gene Expression Regulation, Developmental Humans Mice Mice, Inbred C57BL Multiprotein Complexes - metabolism Protein Binding Transcriptional Activation |
title | Multiple Structural Maintenance of Chromosome Complexes at Transcriptional Regulatory Elements |
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