The Molecular Revolution in Cutaneous Biology: EDC and Locus Control
The epidermal differentiation complex (EDC) locus consists of a cluster of genes important for the terminal differentiation of the epidermis. While early studies identified the functional importance of individual EDC genes, the recognition of the EDC genes as a cluster with its shared biology, homol...
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Veröffentlicht in: | Journal of investigative dermatology 2017-05, Vol.137 (5), p.e101-e104 |
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description | The epidermal differentiation complex (EDC) locus consists of a cluster of genes important for the terminal differentiation of the epidermis. While early studies identified the functional importance of individual EDC genes, the recognition of the EDC genes as a cluster with its shared biology, homology, and physical linkage was pivotal to later studies that investigated the transcriptional regulation of the locus. Evolutionary conservation of the EDC and the transcriptional activation during epidermal differentiation suggested a cis-regulatory mechanism via conserved noncoding elements or enhancers. This line of pursuit led to the identification of CNE 923, an epidermal-specific enhancer that was found to mediate chromatin remodeling of the EDC in an AP-1 dependent manner. These genomic studies, as well as the advent of high-throughput sequencing and genome engineering techniques, have paved the way for future investigation into enhancer-mediated regulatory networks in cutaneous biology. |
doi_str_mv | 10.1016/j.jid.2016.03.046 |
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These genomic studies, as well as the advent of high-throughput sequencing and genome engineering techniques, have paved the way for future investigation into enhancer-mediated regulatory networks in cutaneous biology.</description><identifier>ISSN: 0022-202X</identifier><identifier>EISSN: 1523-1747</identifier><identifier>DOI: 10.1016/j.jid.2016.03.046</identifier><identifier>PMID: 28411839</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Cell Differentiation - genetics ; Chromatin Assembly and Disassembly - genetics ; Enhancer Elements, Genetic - genetics ; Epidermis - physiology ; Genomics - methods ; High-Throughput Nucleotide Sequencing - methods ; Humans ; Molecular Biology - methods ; Transcription Factor AP-1 - genetics</subject><ispartof>Journal of investigative dermatology, 2017-05, Vol.137 (5), p.e101-e104</ispartof><rights>2016 The Authors</rights><rights>Copyright © 2016 The Authors. Published by Elsevier Inc. 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While early studies identified the functional importance of individual EDC genes, the recognition of the EDC genes as a cluster with its shared biology, homology, and physical linkage was pivotal to later studies that investigated the transcriptional regulation of the locus. Evolutionary conservation of the EDC and the transcriptional activation during epidermal differentiation suggested a cis-regulatory mechanism via conserved noncoding elements or enhancers. This line of pursuit led to the identification of CNE 923, an epidermal-specific enhancer that was found to mediate chromatin remodeling of the EDC in an AP-1 dependent manner. These genomic studies, as well as the advent of high-throughput sequencing and genome engineering techniques, have paved the way for future investigation into enhancer-mediated regulatory networks in cutaneous biology.</description><subject>Animals</subject><subject>Cell Differentiation - genetics</subject><subject>Chromatin Assembly and Disassembly - genetics</subject><subject>Enhancer Elements, Genetic - genetics</subject><subject>Epidermis - physiology</subject><subject>Genomics - methods</subject><subject>High-Throughput Nucleotide Sequencing - methods</subject><subject>Humans</subject><subject>Molecular Biology - methods</subject><subject>Transcription Factor AP-1 - genetics</subject><issn>0022-202X</issn><issn>1523-1747</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kF1r2zAUhsVoWbJuP2A3w5e9iXv0YVvarlon_YCUwchgd0KWjzcFx2olO5B_P5WkveyNJMTzvpzzEPKVQk6BllfbfOvanKVnDjwHUX4gc1owvqCVqM7IHICxBQP2Z0Y-xbiFBIpCfiQzJgWlkqs5WW7-Yfboe7RTb0L2C_e-n0bnh8wNWT2NZkA_xezG-d7_PXzPVss6M0Obrb1N37UfxuD7z-S8M33EL6f7gvy-XW3q-8X6591Dfb1eWFGyMZ2yg6oCKEplpOq6hjMwwnDghUAUpWoMMGo4GmmUMh2whndVhbxoWdNafkEuj71PwT9PGEe9c9Fi3x-n1FRKqQqlmEgoPaI2-BgDdvopuJ0JB01Bv8jTW53k6Rd5GrhO8lLm26l-anbYviVebSXgxxHAtOTeYdDROhwsti6gHXXr3Tv1_wGVr35B</recordid><startdate>201705</startdate><enddate>201705</enddate><creator>Oh, Inez Y.</creator><creator>de Guzman Strong, Cristina</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></search><sort><creationdate>201705</creationdate><title>The Molecular Revolution in Cutaneous Biology: EDC and Locus Control</title><author>Oh, Inez Y. ; de Guzman Strong, Cristina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c462t-c48f07700569a89ffb320a4a30354ee469ba021a3ea8a99af02b3f77e35d2bdc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Cell Differentiation - genetics</topic><topic>Chromatin Assembly and Disassembly - genetics</topic><topic>Enhancer Elements, Genetic - genetics</topic><topic>Epidermis - physiology</topic><topic>Genomics - methods</topic><topic>High-Throughput Nucleotide Sequencing - methods</topic><topic>Humans</topic><topic>Molecular Biology - methods</topic><topic>Transcription Factor AP-1 - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oh, Inez Y.</creatorcontrib><creatorcontrib>de Guzman Strong, Cristina</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><jtitle>Journal of investigative dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oh, Inez Y.</au><au>de Guzman Strong, Cristina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Molecular Revolution in Cutaneous Biology: EDC and Locus Control</atitle><jtitle>Journal of investigative dermatology</jtitle><addtitle>J Invest Dermatol</addtitle><date>2017-05</date><risdate>2017</risdate><volume>137</volume><issue>5</issue><spage>e101</spage><epage>e104</epage><pages>e101-e104</pages><issn>0022-202X</issn><eissn>1523-1747</eissn><abstract>The epidermal differentiation complex (EDC) locus consists of a cluster of genes important for the terminal differentiation of the epidermis. While early studies identified the functional importance of individual EDC genes, the recognition of the EDC genes as a cluster with its shared biology, homology, and physical linkage was pivotal to later studies that investigated the transcriptional regulation of the locus. Evolutionary conservation of the EDC and the transcriptional activation during epidermal differentiation suggested a cis-regulatory mechanism via conserved noncoding elements or enhancers. This line of pursuit led to the identification of CNE 923, an epidermal-specific enhancer that was found to mediate chromatin remodeling of the EDC in an AP-1 dependent manner. 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subjects | Animals Cell Differentiation - genetics Chromatin Assembly and Disassembly - genetics Enhancer Elements, Genetic - genetics Epidermis - physiology Genomics - methods High-Throughput Nucleotide Sequencing - methods Humans Molecular Biology - methods Transcription Factor AP-1 - genetics |
title | The Molecular Revolution in Cutaneous Biology: EDC and Locus Control |
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