Epigenetic Regulation of Gene Expression in Keratinocytes
The nucleus is a complex and highly compartmentalized organelle, which undergoes major organization changes during cell differentiation, allowing cells to become specialized and fulfill their functions. During terminal differentiation of the epidermal keratinocytes, the nucleus undergoes a programme...
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Veröffentlicht in: | Journal of investigative dermatology 2012-11, Vol.132 (11), p.2505-2521 |
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creator | Botchkarev, Vladimir A. Gdula, Michal R. Mardaryev, Andrei N. Sharov, Andrei A. Fessing, Michael Y. |
description | The nucleus is a complex and highly compartmentalized organelle, which undergoes major organization changes during cell differentiation, allowing cells to become specialized and fulfill their functions. During terminal differentiation of the epidermal keratinocytes, the nucleus undergoes a programmed transformation from active status, associated with execution of the genetic programs of cornification and epidermal barrier formation, to a fully inactive condition and becomes a part of the keratinized cells of the cornified layer. Tremendous progress achieved within the past two decades in understanding the biology of the nucleus and epigenetic mechanisms controlling gene expression allowed defining several levels in the regulation of cell differentiation–associated gene expression programs, including an accessibility of the gene regulatory regions to DNA–protein interactions, covalent DNA and histone modifications, and ATP-dependent chromatin remodeling, as well as higher-order chromatin remodeling and nuclear compartmentalization of the genes and transcription machinery. Here, we integrate our current knowledge of the mechanisms controlling gene expression during terminal keratinocyte differentiation with distinct levels of chromatin organization and remodeling. We also propose directions to further explore the role of epigenetic mechanisms and their interactions with other regulatory systems in the control of keratinocyte differentiation in normal and diseased skin. |
doi_str_mv | 10.1038/jid.2012.182 |
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During terminal differentiation of the epidermal keratinocytes, the nucleus undergoes a programmed transformation from active status, associated with execution of the genetic programs of cornification and epidermal barrier formation, to a fully inactive condition and becomes a part of the keratinized cells of the cornified layer. Tremendous progress achieved within the past two decades in understanding the biology of the nucleus and epigenetic mechanisms controlling gene expression allowed defining several levels in the regulation of cell differentiation–associated gene expression programs, including an accessibility of the gene regulatory regions to DNA–protein interactions, covalent DNA and histone modifications, and ATP-dependent chromatin remodeling, as well as higher-order chromatin remodeling and nuclear compartmentalization of the genes and transcription machinery. Here, we integrate our current knowledge of the mechanisms controlling gene expression during terminal keratinocyte differentiation with distinct levels of chromatin organization and remodeling. We also propose directions to further explore the role of epigenetic mechanisms and their interactions with other regulatory systems in the control of keratinocyte differentiation in normal and diseased skin.</description><identifier>ISSN: 0022-202X</identifier><identifier>EISSN: 1523-1747</identifier><identifier>DOI: 10.1038/jid.2012.182</identifier><identifier>PMID: 22763788</identifier><identifier>CODEN: JIDEAE</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Animals ; Biological and medical sciences ; Cell Differentiation - physiology ; Cell Nucleus - physiology ; Chromatin remodeling ; Dermatology ; Differentiation ; DNA ; Epigenesis, Genetic - physiology ; epigenetics ; Gene expression ; Gene Expression Regulation - physiology ; Histones ; Humans ; Keratinocytes ; Keratinocytes - cytology ; Keratinocytes - physiology ; Medical sciences ; Nuclei ; Organelles ; Regulatory sequences ; Skin diseases ; Transcription ; Transformation</subject><ispartof>Journal of investigative dermatology, 2012-11, Vol.132 (11), p.2505-2521</ispartof><rights>2012 The Society for Investigative Dermatology, Inc</rights><rights>2015 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Nov 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c522t-c356a31871fb26e72063825f5f2d064e9f10e2a14307a7d41add49d227852bcb3</citedby><cites>FETCH-LOGICAL-c522t-c356a31871fb26e72063825f5f2d064e9f10e2a14307a7d41add49d227852bcb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/1112175529?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,64385,64387,64389,72469</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26506819$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22763788$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Botchkarev, Vladimir A.</creatorcontrib><creatorcontrib>Gdula, Michal R.</creatorcontrib><creatorcontrib>Mardaryev, Andrei N.</creatorcontrib><creatorcontrib>Sharov, Andrei A.</creatorcontrib><creatorcontrib>Fessing, Michael Y.</creatorcontrib><title>Epigenetic Regulation of Gene Expression in Keratinocytes</title><title>Journal of investigative dermatology</title><addtitle>J Invest Dermatol</addtitle><description>The nucleus is a complex and highly compartmentalized organelle, which undergoes major organization changes during cell differentiation, allowing cells to become specialized and fulfill their functions. During terminal differentiation of the epidermal keratinocytes, the nucleus undergoes a programmed transformation from active status, associated with execution of the genetic programs of cornification and epidermal barrier formation, to a fully inactive condition and becomes a part of the keratinized cells of the cornified layer. Tremendous progress achieved within the past two decades in understanding the biology of the nucleus and epigenetic mechanisms controlling gene expression allowed defining several levels in the regulation of cell differentiation–associated gene expression programs, including an accessibility of the gene regulatory regions to DNA–protein interactions, covalent DNA and histone modifications, and ATP-dependent chromatin remodeling, as well as higher-order chromatin remodeling and nuclear compartmentalization of the genes and transcription machinery. Here, we integrate our current knowledge of the mechanisms controlling gene expression during terminal keratinocyte differentiation with distinct levels of chromatin organization and remodeling. We also propose directions to further explore the role of epigenetic mechanisms and their interactions with other regulatory systems in the control of keratinocyte differentiation in normal and diseased skin.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell Differentiation - physiology</subject><subject>Cell Nucleus - physiology</subject><subject>Chromatin remodeling</subject><subject>Dermatology</subject><subject>Differentiation</subject><subject>DNA</subject><subject>Epigenesis, Genetic - physiology</subject><subject>epigenetics</subject><subject>Gene expression</subject><subject>Gene Expression Regulation - physiology</subject><subject>Histones</subject><subject>Humans</subject><subject>Keratinocytes</subject><subject>Keratinocytes - cytology</subject><subject>Keratinocytes - physiology</subject><subject>Medical sciences</subject><subject>Nuclei</subject><subject>Organelles</subject><subject>Regulatory sequences</subject><subject>Skin diseases</subject><subject>Transcription</subject><subject>Transformation</subject><issn>0022-202X</issn><issn>1523-1747</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqNkU2LFDEQhoMo7uzqzbMMiLAHe0xVdz76siDLuIoLgih4C5l09ZihJxmT7sX992accf3Ag6dA1UPlrXoYewJ8AbzWLze-WyAHXIDGe2wGAusKVKPusxnniBVy_HzCTnPecA6yEfohO0FUslZaz1i73Pk1BRq9m3-g9TTY0ccwj_38qlTny2-7RDnvSz7M31Eq7RDd7Uj5EXvQ2yHT4-N7xj69Xn68fFNdv796e_nqunICcaxcLaStQSvoVyhJIZe1RtGLHjsuG2p74IQWmporq7oGbNc1bVcSaoErt6rP2MVh7m5abalzFMZkB7NLfmvTrYnWmz87wX8x63hjail4o7AMOD8OSPHrRHk0W58dDYMNFKdsAFSJh6qF_0ABZQmmm4I--wvdxCmFcokfFCghsC3UiwPlUsw5UX-XG7jZ6zNFn9nrM0VfwZ_-vusd_NNXAZ4fAZudHfpkg_P5F1dWlhr2_8oDR8XMjadksvMUHHU-kRtNF_2_E3wHQ7yzhg</recordid><startdate>20121101</startdate><enddate>20121101</enddate><creator>Botchkarev, Vladimir A.</creator><creator>Gdula, Michal R.</creator><creator>Mardaryev, Andrei N.</creator><creator>Sharov, Andrei A.</creator><creator>Fessing, Michael Y.</creator><general>Elsevier Inc</general><general>Nature Publishing Group</general><general>Elsevier Limited</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</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>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>7TM</scope><scope>5PM</scope></search><sort><creationdate>20121101</creationdate><title>Epigenetic Regulation of Gene Expression in Keratinocytes</title><author>Botchkarev, Vladimir A. ; 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During terminal differentiation of the epidermal keratinocytes, the nucleus undergoes a programmed transformation from active status, associated with execution of the genetic programs of cornification and epidermal barrier formation, to a fully inactive condition and becomes a part of the keratinized cells of the cornified layer. Tremendous progress achieved within the past two decades in understanding the biology of the nucleus and epigenetic mechanisms controlling gene expression allowed defining several levels in the regulation of cell differentiation–associated gene expression programs, including an accessibility of the gene regulatory regions to DNA–protein interactions, covalent DNA and histone modifications, and ATP-dependent chromatin remodeling, as well as higher-order chromatin remodeling and nuclear compartmentalization of the genes and transcription machinery. 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subjects | Animals Biological and medical sciences Cell Differentiation - physiology Cell Nucleus - physiology Chromatin remodeling Dermatology Differentiation DNA Epigenesis, Genetic - physiology epigenetics Gene expression Gene Expression Regulation - physiology Histones Humans Keratinocytes Keratinocytes - cytology Keratinocytes - physiology Medical sciences Nuclei Organelles Regulatory sequences Skin diseases Transcription Transformation |
title | Epigenetic Regulation of Gene Expression in Keratinocytes |
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