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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Journal of biological chemistry 2012-06, Vol.287 (23), p.19148-19157
Hauptverfasser: Wratting, Daniel, Thistlethwaite, Angela, Harris, Michael, Zeef, Leo A.H., Millar, Catherine B.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 19157
container_issue 23
container_start_page 19148
container_title The Journal of biological chemistry
container_volume 287
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
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3365947</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0021925820499727</els_id><sourcerecordid>1018636023</sourcerecordid><originalsourceid>FETCH-LOGICAL-c443t-b288c01644145bdb62fd2a38a174fb0a8c6d5f5fe216889ed764117d0e582d203</originalsourceid><addsrcrecordid>eNp1kD1PwzAQhi0EouVjZkMZWdL6bCdxFqSqohSpiKVIiMVK7At11cbFTirx70nVUsHALTfcc--dHkJugA6AZmK4LPXgGQAGHLI8pyekD1TymCfwdkr6lDKIc5bIHrkIYUm7Ejmckx5jIu-YpE_iUTR2dUC_RRNN2lo31tVR5XzULDCastHgPRpHc_RrW7fhipxVxSrg9aFfktfJw3w8jWcvj0_j0SzWQvAmLpmUmkIqBIikNGXKKsMKLgvIRFXSQurUJFVSIYNUyhxNlgqAzFBMJDOM8ktyv8_dtOUajca68cVKbbxdF_5LucKqv5PaLtSH2yrO0yQXWRdwdwjw7rPF0Ki1DRpXq6JG1wYFFGTKU8p4hw73qPYuBI_V8QxQtZOsOslqJ1ntJXcbt7-_O_I_Vjsg3wPYOdpa9Cpoi7VGYz3qRhln_w3_Bt-fiYE</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1018636023</pqid></control><display><type>article</type><title>A Conserved Function for the H2A.Z C Terminus</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Wratting, Daniel ; Thistlethwaite, Angela ; Harris, Michael ; Zeef, Leo A.H. ; Millar, Catherine B.</creator><creatorcontrib>Wratting, Daniel ; Thistlethwaite, Angela ; Harris, Michael ; Zeef, Leo A.H. ; Millar, Catherine B.</creatorcontrib><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><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>
fulltext fulltext
identifier ISSN: 0021-9258
ispartof The Journal of biological chemistry, 2012-06, Vol.287 (23), p.19148-19157
issn 0021-9258
1083-351X
1083-351X
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3365947
source MEDLINE; EZB-FREE-00999 freely available EZB journals; PubMed Central; Alma/SFX Local Collection
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T04%3A28%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20Conserved%20Function%20for%20the%20H2A.Z%20C%20Terminus&rft.jtitle=The%20Journal%20of%20biological%20chemistry&rft.au=Wratting,%20Daniel&rft.date=2012-06-01&rft.volume=287&rft.issue=23&rft.spage=19148&rft.epage=19157&rft.pages=19148-19157&rft.issn=0021-9258&rft.eissn=1083-351X&rft_id=info:doi/10.1074/jbc.M111.317990&rft_dat=%3Cproquest_pubme%3E1018636023%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1018636023&rft_id=info:pmid/22493515&rft_els_id=S0021925820499727&rfr_iscdi=true