A Conserved Function for the H2A.Z C Terminus
Histone H2A variants generate diversity in chromatin structure and functions, as nucleosomes containing variant H2A histones have altered physical, chemical, and biological properties. H2A.Z is an evolutionarily ancient and highly conserved H2A variant that regulates processes ranging from gene expr...
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Veröffentlicht in: | The Journal of biological chemistry 2012-06, Vol.287 (23), p.19148-19157 |
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creator | Wratting, Daniel Thistlethwaite, Angela Harris, Michael Zeef, Leo A.H. Millar, Catherine B. |
description | Histone H2A variants generate diversity in chromatin structure and functions, as nucleosomes containing variant H2A histones have altered physical, chemical, and biological properties. H2A.Z is an evolutionarily ancient and highly conserved H2A variant that regulates processes ranging from gene expression to the DNA damage response. Here we find that the unstructured portion of the C-terminal tail of H2A.Z is required for the normal functions of this histone variant in budding yeast. We have also identified a novel splice isoform of the human H2A.Z-2 gene that encodes a C-terminally truncated H2A.Z protein that is similar to the truncation mutants we identified in yeast. The short forms of H2A.Z in both yeast and human cells are more loosely associated with chromatin than the full-length proteins, indicating a conserved function for the H2A.Z C-terminal tail in regulating the association of H2A.Z with nucleosomes.
The H2A variant H2A.Z is an important regulatory component of chromatin.
A novel form of human H2A.Z and mutants of yeast H2A.Z that share truncated C termini have altered properties.
The C-terminal tail of histone H2A.Z is important for its stable association with nucleosomes.
The strength of H2A.Z's association with nucleosomes is key to the biological functions of this histone variant. |
doi_str_mv | 10.1074/jbc.M111.317990 |
format | Article |
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The H2A variant H2A.Z is an important regulatory component of chromatin.
A novel form of human H2A.Z and mutants of yeast H2A.Z that share truncated C termini have altered properties.
The C-terminal tail of histone H2A.Z is important for its stable association with nucleosomes.
The strength of H2A.Z's association with nucleosomes is key to the biological functions of this histone variant.</description><identifier>ISSN: 0021-9258</identifier><identifier>ISSN: 1083-351X</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M111.317990</identifier><identifier>PMID: 22493515</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Alternative Splicing - physiology ; Cell Line ; Chromatin ; Chromatin Immunoprecipitation (ChiP) ; Chromatin Regulation ; Chromatin Structure ; DNA and Chromosomes ; Histone Variant ; Histones ; Histones - genetics ; Histones - metabolism ; Humans ; Nucleosomes - genetics ; Nucleosomes - metabolism ; Protein Isoforms - genetics ; Protein Isoforms - metabolism ; Protein Structure, Tertiary ; Saccharomyces cerevisiae - genetics ; Saccharomyces cerevisiae - metabolism ; Saccharomyces cerevisiae Proteins - genetics ; Saccharomyces cerevisiae Proteins - metabolism</subject><ispartof>The Journal of biological chemistry, 2012-06, Vol.287 (23), p.19148-19157</ispartof><rights>2012 © 2012 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><rights>2012 by The American Society for Biochemistry and Molecular Biology, Inc. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-b288c01644145bdb62fd2a38a174fb0a8c6d5f5fe216889ed764117d0e582d203</citedby><cites>FETCH-LOGICAL-c443t-b288c01644145bdb62fd2a38a174fb0a8c6d5f5fe216889ed764117d0e582d203</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/PMC3365947/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3365947/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,883,27907,27908,53774,53776</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22493515$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wratting, Daniel</creatorcontrib><creatorcontrib>Thistlethwaite, Angela</creatorcontrib><creatorcontrib>Harris, Michael</creatorcontrib><creatorcontrib>Zeef, Leo A.H.</creatorcontrib><creatorcontrib>Millar, Catherine B.</creatorcontrib><title>A Conserved Function for the H2A.Z C Terminus</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Histone H2A variants generate diversity in chromatin structure and functions, as nucleosomes containing variant H2A histones have altered physical, chemical, and biological properties. H2A.Z is an evolutionarily ancient and highly conserved H2A variant that regulates processes ranging from gene expression to the DNA damage response. Here we find that the unstructured portion of the C-terminal tail of H2A.Z is required for the normal functions of this histone variant in budding yeast. We have also identified a novel splice isoform of the human H2A.Z-2 gene that encodes a C-terminally truncated H2A.Z protein that is similar to the truncation mutants we identified in yeast. The short forms of H2A.Z in both yeast and human cells are more loosely associated with chromatin than the full-length proteins, indicating a conserved function for the H2A.Z C-terminal tail in regulating the association of H2A.Z with nucleosomes.
The H2A variant H2A.Z is an important regulatory component of chromatin.
A novel form of human H2A.Z and mutants of yeast H2A.Z that share truncated C termini have altered properties.
The C-terminal tail of histone H2A.Z is important for its stable association with nucleosomes.
The strength of H2A.Z's association with nucleosomes is key to the biological functions of this histone variant.</description><subject>Alternative Splicing - physiology</subject><subject>Cell Line</subject><subject>Chromatin</subject><subject>Chromatin Immunoprecipitation (ChiP)</subject><subject>Chromatin Regulation</subject><subject>Chromatin Structure</subject><subject>DNA and Chromosomes</subject><subject>Histone Variant</subject><subject>Histones</subject><subject>Histones - genetics</subject><subject>Histones - metabolism</subject><subject>Humans</subject><subject>Nucleosomes - genetics</subject><subject>Nucleosomes - metabolism</subject><subject>Protein Isoforms - genetics</subject><subject>Protein Isoforms - metabolism</subject><subject>Protein Structure, Tertiary</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Saccharomyces cerevisiae - metabolism</subject><subject>Saccharomyces cerevisiae Proteins - genetics</subject><subject>Saccharomyces cerevisiae Proteins - metabolism</subject><issn>0021-9258</issn><issn>1083-351X</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kD1PwzAQhi0EouVjZkMZWdL6bCdxFqSqohSpiKVIiMVK7At11cbFTirx70nVUsHALTfcc--dHkJugA6AZmK4LPXgGQAGHLI8pyekD1TymCfwdkr6lDKIc5bIHrkIYUm7Ejmckx5jIu-YpE_iUTR2dUC_RRNN2lo31tVR5XzULDCastHgPRpHc_RrW7fhipxVxSrg9aFfktfJw3w8jWcvj0_j0SzWQvAmLpmUmkIqBIikNGXKKsMKLgvIRFXSQurUJFVSIYNUyhxNlgqAzFBMJDOM8ktyv8_dtOUajca68cVKbbxdF_5LucKqv5PaLtSH2yrO0yQXWRdwdwjw7rPF0Ki1DRpXq6JG1wYFFGTKU8p4hw73qPYuBI_V8QxQtZOsOslqJ1ntJXcbt7-_O_I_Vjsg3wPYOdpa9Cpoi7VGYz3qRhln_w3_Bt-fiYE</recordid><startdate>20120601</startdate><enddate>20120601</enddate><creator>Wratting, Daniel</creator><creator>Thistlethwaite, Angela</creator><creator>Harris, Michael</creator><creator>Zeef, Leo A.H.</creator><creator>Millar, Catherine B.</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</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>20120601</creationdate><title>A Conserved Function for the H2A.Z C Terminus</title><author>Wratting, Daniel ; Thistlethwaite, Angela ; Harris, Michael ; Zeef, Leo A.H. ; Millar, Catherine B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-b288c01644145bdb62fd2a38a174fb0a8c6d5f5fe216889ed764117d0e582d203</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Alternative Splicing - physiology</topic><topic>Cell Line</topic><topic>Chromatin</topic><topic>Chromatin Immunoprecipitation (ChiP)</topic><topic>Chromatin Regulation</topic><topic>Chromatin Structure</topic><topic>DNA and Chromosomes</topic><topic>Histone Variant</topic><topic>Histones</topic><topic>Histones - genetics</topic><topic>Histones - metabolism</topic><topic>Humans</topic><topic>Nucleosomes - genetics</topic><topic>Nucleosomes - metabolism</topic><topic>Protein Isoforms - genetics</topic><topic>Protein Isoforms - metabolism</topic><topic>Protein Structure, Tertiary</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Saccharomyces cerevisiae - metabolism</topic><topic>Saccharomyces cerevisiae Proteins - genetics</topic><topic>Saccharomyces cerevisiae Proteins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wratting, Daniel</creatorcontrib><creatorcontrib>Thistlethwaite, Angela</creatorcontrib><creatorcontrib>Harris, Michael</creatorcontrib><creatorcontrib>Zeef, Leo A.H.</creatorcontrib><creatorcontrib>Millar, Catherine B.</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>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wratting, Daniel</au><au>Thistlethwaite, Angela</au><au>Harris, Michael</au><au>Zeef, Leo A.H.</au><au>Millar, Catherine B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Conserved Function for the H2A.Z C Terminus</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2012-06-01</date><risdate>2012</risdate><volume>287</volume><issue>23</issue><spage>19148</spage><epage>19157</epage><pages>19148-19157</pages><issn>0021-9258</issn><issn>1083-351X</issn><eissn>1083-351X</eissn><abstract>Histone H2A variants generate diversity in chromatin structure and functions, as nucleosomes containing variant H2A histones have altered physical, chemical, and biological properties. H2A.Z is an evolutionarily ancient and highly conserved H2A variant that regulates processes ranging from gene expression to the DNA damage response. Here we find that the unstructured portion of the C-terminal tail of H2A.Z is required for the normal functions of this histone variant in budding yeast. We have also identified a novel splice isoform of the human H2A.Z-2 gene that encodes a C-terminally truncated H2A.Z protein that is similar to the truncation mutants we identified in yeast. The short forms of H2A.Z in both yeast and human cells are more loosely associated with chromatin than the full-length proteins, indicating a conserved function for the H2A.Z C-terminal tail in regulating the association of H2A.Z with nucleosomes.
The H2A variant H2A.Z is an important regulatory component of chromatin.
A novel form of human H2A.Z and mutants of yeast H2A.Z that share truncated C termini have altered properties.
The C-terminal tail of histone H2A.Z is important for its stable association with nucleosomes.
The strength of H2A.Z's association with nucleosomes is key to the biological functions of this histone variant.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>22493515</pmid><doi>10.1074/jbc.M111.317990</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alternative Splicing - physiology Cell Line Chromatin Chromatin Immunoprecipitation (ChiP) Chromatin Regulation Chromatin Structure DNA and Chromosomes Histone Variant Histones Histones - genetics Histones - metabolism Humans Nucleosomes - genetics Nucleosomes - metabolism Protein Isoforms - genetics Protein Isoforms - metabolism Protein Structure, Tertiary Saccharomyces cerevisiae - genetics Saccharomyces cerevisiae - metabolism Saccharomyces cerevisiae Proteins - genetics Saccharomyces cerevisiae Proteins - metabolism |
title | A Conserved Function for the H2A.Z C Terminus |
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