Distinct chromatin signature of histone H3 variant H3.3 in human cells

Actively transcribed regions of the genome have been found enriched for the histone H3 variant H3.3. This variant is incorporated into nucleosomes throughout the cell cycle whereas the canonical isoforms are predominately deposited in association with replication. In order to obtain a global picture...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nucleus (Austin, Tex.) Tex.), 2014-09, Vol.5 (5), p.449-461
Hauptverfasser: Snyers, Luc, Zupkovitz, Gordin, Almeder, Marlene, Fliesser, Marianne, Stoisser, Anja, Weipoltshammer, Klara, Schöfer, Christian
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 461
container_issue 5
container_start_page 449
container_title Nucleus (Austin, Tex.)
container_volume 5
creator Snyers, Luc
Zupkovitz, Gordin
Almeder, Marlene
Fliesser, Marianne
Stoisser, Anja
Weipoltshammer, Klara
Schöfer, Christian
description Actively transcribed regions of the genome have been found enriched for the histone H3 variant H3.3. This variant is incorporated into nucleosomes throughout the cell cycle whereas the canonical isoforms are predominately deposited in association with replication. In order to obtain a global picture of the deposition pattern at the single cell level we expressed H3.3 in both normal and malignant human cells and analyzed nuclei using conventional and structured illumination imaging (SIM). We found that the distribution pattern of H3.3 in interphase differs from that of the canonical histone H3 variants and this difference is conveyed to mitotic chromosomes which display a distinct H3.3 banding pattern. Histone H3.3 localization positively correlated with markers for transcriptionally active chromatin and, notably, H3.3 was almost completely absent from the inactive X chromosome. Collectively, our data show that histone variant H3.3 occupies distinct intranuclear chromatin domains and that these genomic loci are associated with gene expression.
doi_str_mv 10.4161/nucl.36229
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2524243141</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1634725614</sourcerecordid><originalsourceid>FETCH-LOGICAL-c402t-a46a62ac106963ba28d4f63e505c6c1b1ebd0cf08b498e32b47641cb8008ced93</originalsourceid><addsrcrecordid>eNqFkF1LwzAUhoMobszd-AMklyJ05uM0bS9lOicMvNHrkKapi7TJTFpl_97OzV0Jnpvzwnl4OTwIXVIyAyroret1M-OCseIEjWkBRUIJsNNj5jBC0xjfyTAAGUnpORqxFHJGi2yMFvc2dtbpDut18K0aMo72zamuDwb7Gq-Hu3cGLzn-VMEq1w1xxvHArftWOaxN08QLdFarJprpYU_Q6-LhZb5MVs-PT_O7VaKBsC5RIJRgSlMiCsFLxfIKasFNSlItNC2pKSuia5KXUOSGsxIyAVSXOSG5NlXBJ-h637sJ_qM3sZOtjbsPlDO-j5KlDBhwCvRflAoOGUsFhQG92aM6-BiDqeUm2FaFraRE7izLnWX5Y3mArw69fdma6oj-Oh2AdA9YV_vQqi8fmkp2atv4UAfltI2S_1H8DQj2iIo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1634725614</pqid></control><display><type>article</type><title>Distinct chromatin signature of histone H3 variant H3.3 in human cells</title><source>Taylor &amp; Francis Open Access</source><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>Snyers, Luc ; Zupkovitz, Gordin ; Almeder, Marlene ; Fliesser, Marianne ; Stoisser, Anja ; Weipoltshammer, Klara ; Schöfer, Christian</creator><creatorcontrib>Snyers, Luc ; Zupkovitz, Gordin ; Almeder, Marlene ; Fliesser, Marianne ; Stoisser, Anja ; Weipoltshammer, Klara ; Schöfer, Christian</creatorcontrib><description>Actively transcribed regions of the genome have been found enriched for the histone H3 variant H3.3. This variant is incorporated into nucleosomes throughout the cell cycle whereas the canonical isoforms are predominately deposited in association with replication. In order to obtain a global picture of the deposition pattern at the single cell level we expressed H3.3 in both normal and malignant human cells and analyzed nuclei using conventional and structured illumination imaging (SIM). We found that the distribution pattern of H3.3 in interphase differs from that of the canonical histone H3 variants and this difference is conveyed to mitotic chromosomes which display a distinct H3.3 banding pattern. Histone H3.3 localization positively correlated with markers for transcriptionally active chromatin and, notably, H3.3 was almost completely absent from the inactive X chromosome. Collectively, our data show that histone variant H3.3 occupies distinct intranuclear chromatin domains and that these genomic loci are associated with gene expression.</description><identifier>ISSN: 1949-1034</identifier><identifier>ISSN: 1949-1042</identifier><identifier>EISSN: 1949-1042</identifier><identifier>DOI: 10.4161/nucl.36229</identifier><identifier>PMID: 25482197</identifier><language>eng</language><publisher>United States: Taylor &amp; Francis</publisher><subject>Cell Nucleus - genetics ; chromatin ; Chromatin - genetics ; Chromosomes, Human, X - genetics ; gene expression ; Gene Expression Regulation ; genome ; Genome, Human ; genomics ; histones ; Histones - genetics ; Humans ; interphase ; lighting ; mitosis ; nuclear architecture ; nucleosomes ; Nucleosomes - genetics ; Single-Cell Analysis ; superresolution imaging ; transcription ; transcription (genetics) ; Transcription, Genetic</subject><ispartof>Nucleus (Austin, Tex.), 2014-09, Vol.5 (5), p.449-461</ispartof><rights>Copyright © 2014 Landes Bioscience 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c402t-a46a62ac106963ba28d4f63e505c6c1b1ebd0cf08b498e32b47641cb8008ced93</citedby><cites>FETCH-LOGICAL-c402t-a46a62ac106963ba28d4f63e505c6c1b1ebd0cf08b498e32b47641cb8008ced93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.4161/nucl.36229$$EPDF$$P50$$Ginformaworld$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.4161/nucl.36229$$EHTML$$P50$$Ginformaworld$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,27479,27901,27902,59116,59117</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25482197$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Snyers, Luc</creatorcontrib><creatorcontrib>Zupkovitz, Gordin</creatorcontrib><creatorcontrib>Almeder, Marlene</creatorcontrib><creatorcontrib>Fliesser, Marianne</creatorcontrib><creatorcontrib>Stoisser, Anja</creatorcontrib><creatorcontrib>Weipoltshammer, Klara</creatorcontrib><creatorcontrib>Schöfer, Christian</creatorcontrib><title>Distinct chromatin signature of histone H3 variant H3.3 in human cells</title><title>Nucleus (Austin, Tex.)</title><addtitle>Nucleus</addtitle><description>Actively transcribed regions of the genome have been found enriched for the histone H3 variant H3.3. This variant is incorporated into nucleosomes throughout the cell cycle whereas the canonical isoforms are predominately deposited in association with replication. In order to obtain a global picture of the deposition pattern at the single cell level we expressed H3.3 in both normal and malignant human cells and analyzed nuclei using conventional and structured illumination imaging (SIM). We found that the distribution pattern of H3.3 in interphase differs from that of the canonical histone H3 variants and this difference is conveyed to mitotic chromosomes which display a distinct H3.3 banding pattern. Histone H3.3 localization positively correlated with markers for transcriptionally active chromatin and, notably, H3.3 was almost completely absent from the inactive X chromosome. Collectively, our data show that histone variant H3.3 occupies distinct intranuclear chromatin domains and that these genomic loci are associated with gene expression.</description><subject>Cell Nucleus - genetics</subject><subject>chromatin</subject><subject>Chromatin - genetics</subject><subject>Chromosomes, Human, X - genetics</subject><subject>gene expression</subject><subject>Gene Expression Regulation</subject><subject>genome</subject><subject>Genome, Human</subject><subject>genomics</subject><subject>histones</subject><subject>Histones - genetics</subject><subject>Humans</subject><subject>interphase</subject><subject>lighting</subject><subject>mitosis</subject><subject>nuclear architecture</subject><subject>nucleosomes</subject><subject>Nucleosomes - genetics</subject><subject>Single-Cell Analysis</subject><subject>superresolution imaging</subject><subject>transcription</subject><subject>transcription (genetics)</subject><subject>Transcription, Genetic</subject><issn>1949-1034</issn><issn>1949-1042</issn><issn>1949-1042</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>0YH</sourceid><sourceid>EIF</sourceid><recordid>eNqFkF1LwzAUhoMobszd-AMklyJ05uM0bS9lOicMvNHrkKapi7TJTFpl_97OzV0Jnpvzwnl4OTwIXVIyAyroret1M-OCseIEjWkBRUIJsNNj5jBC0xjfyTAAGUnpORqxFHJGi2yMFvc2dtbpDut18K0aMo72zamuDwb7Gq-Hu3cGLzn-VMEq1w1xxvHArftWOaxN08QLdFarJprpYU_Q6-LhZb5MVs-PT_O7VaKBsC5RIJRgSlMiCsFLxfIKasFNSlItNC2pKSuia5KXUOSGsxIyAVSXOSG5NlXBJ-h637sJ_qM3sZOtjbsPlDO-j5KlDBhwCvRflAoOGUsFhQG92aM6-BiDqeUm2FaFraRE7izLnWX5Y3mArw69fdma6oj-Oh2AdA9YV_vQqi8fmkp2atv4UAfltI2S_1H8DQj2iIo</recordid><startdate>20140901</startdate><enddate>20140901</enddate><creator>Snyers, Luc</creator><creator>Zupkovitz, Gordin</creator><creator>Almeder, Marlene</creator><creator>Fliesser, Marianne</creator><creator>Stoisser, Anja</creator><creator>Weipoltshammer, Klara</creator><creator>Schöfer, Christian</creator><general>Taylor &amp; Francis</general><scope>0YH</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>7S9</scope><scope>L.6</scope></search><sort><creationdate>20140901</creationdate><title>Distinct chromatin signature of histone H3 variant H3.3 in human cells</title><author>Snyers, Luc ; Zupkovitz, Gordin ; Almeder, Marlene ; Fliesser, Marianne ; Stoisser, Anja ; Weipoltshammer, Klara ; Schöfer, Christian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c402t-a46a62ac106963ba28d4f63e505c6c1b1ebd0cf08b498e32b47641cb8008ced93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Cell Nucleus - genetics</topic><topic>chromatin</topic><topic>Chromatin - genetics</topic><topic>Chromosomes, Human, X - genetics</topic><topic>gene expression</topic><topic>Gene Expression Regulation</topic><topic>genome</topic><topic>Genome, Human</topic><topic>genomics</topic><topic>histones</topic><topic>Histones - genetics</topic><topic>Humans</topic><topic>interphase</topic><topic>lighting</topic><topic>mitosis</topic><topic>nuclear architecture</topic><topic>nucleosomes</topic><topic>Nucleosomes - genetics</topic><topic>Single-Cell Analysis</topic><topic>superresolution imaging</topic><topic>transcription</topic><topic>transcription (genetics)</topic><topic>Transcription, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Snyers, Luc</creatorcontrib><creatorcontrib>Zupkovitz, Gordin</creatorcontrib><creatorcontrib>Almeder, Marlene</creatorcontrib><creatorcontrib>Fliesser, Marianne</creatorcontrib><creatorcontrib>Stoisser, Anja</creatorcontrib><creatorcontrib>Weipoltshammer, Klara</creatorcontrib><creatorcontrib>Schöfer, Christian</creatorcontrib><collection>Taylor &amp; Francis 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>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Nucleus (Austin, Tex.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Snyers, Luc</au><au>Zupkovitz, Gordin</au><au>Almeder, Marlene</au><au>Fliesser, Marianne</au><au>Stoisser, Anja</au><au>Weipoltshammer, Klara</au><au>Schöfer, Christian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Distinct chromatin signature of histone H3 variant H3.3 in human cells</atitle><jtitle>Nucleus (Austin, Tex.)</jtitle><addtitle>Nucleus</addtitle><date>2014-09-01</date><risdate>2014</risdate><volume>5</volume><issue>5</issue><spage>449</spage><epage>461</epage><pages>449-461</pages><issn>1949-1034</issn><issn>1949-1042</issn><eissn>1949-1042</eissn><abstract>Actively transcribed regions of the genome have been found enriched for the histone H3 variant H3.3. This variant is incorporated into nucleosomes throughout the cell cycle whereas the canonical isoforms are predominately deposited in association with replication. In order to obtain a global picture of the deposition pattern at the single cell level we expressed H3.3 in both normal and malignant human cells and analyzed nuclei using conventional and structured illumination imaging (SIM). We found that the distribution pattern of H3.3 in interphase differs from that of the canonical histone H3 variants and this difference is conveyed to mitotic chromosomes which display a distinct H3.3 banding pattern. Histone H3.3 localization positively correlated with markers for transcriptionally active chromatin and, notably, H3.3 was almost completely absent from the inactive X chromosome. Collectively, our data show that histone variant H3.3 occupies distinct intranuclear chromatin domains and that these genomic loci are associated with gene expression.</abstract><cop>United States</cop><pub>Taylor &amp; Francis</pub><pmid>25482197</pmid><doi>10.4161/nucl.36229</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1949-1034
ispartof Nucleus (Austin, Tex.), 2014-09, Vol.5 (5), p.449-461
issn 1949-1034
1949-1042
1949-1042
language eng
recordid cdi_proquest_miscellaneous_2524243141
source Taylor & Francis Open Access; MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Cell Nucleus - genetics
chromatin
Chromatin - genetics
Chromosomes, Human, X - genetics
gene expression
Gene Expression Regulation
genome
Genome, Human
genomics
histones
Histones - genetics
Humans
interphase
lighting
mitosis
nuclear architecture
nucleosomes
Nucleosomes - genetics
Single-Cell Analysis
superresolution imaging
transcription
transcription (genetics)
Transcription, Genetic
title Distinct chromatin signature of histone H3 variant H3.3 in human cells
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T08%3A46%3A48IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Distinct%20chromatin%20signature%20of%20histone%20H3%20variant%20H3.3%20in%20human%20cells&rft.jtitle=Nucleus%20(Austin,%20Tex.)&rft.au=Snyers,%20Luc&rft.date=2014-09-01&rft.volume=5&rft.issue=5&rft.spage=449&rft.epage=461&rft.pages=449-461&rft.issn=1949-1034&rft.eissn=1949-1042&rft_id=info:doi/10.4161/nucl.36229&rft_dat=%3Cproquest_cross%3E1634725614%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1634725614&rft_id=info:pmid/25482197&rfr_iscdi=true