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Microarray Analysis Reveals Potential Biological Functions of Histone H2B Monoubiquitination
Histone H2B monoubiquitination is a key histone modification that has significant effects on chromatin higher-order structure and gene transcription. Multiple biological processes have been suggested to be tightly related to the dynamics of H2B monoubiquitination. However, a comprehensive understand...
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Published in: | PloS one 2015-07, Vol.10 (7), p.e0133444-e0133444 |
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creator | Wu, You Chen, Ping Jing, Yuanya Wang, Chen Men, Yu-Long Zhan, Wang Wang, Qiang Gan, Zhixue Huang, Jin Xie, Kun Mi, Jiangsheng Yu, Chenghua Yu, Xiuqing Chen, Pei-Chao Chang, Jian-Feng Cai, Fengfeng Chen, Su |
description | Histone H2B monoubiquitination is a key histone modification that has significant effects on chromatin higher-order structure and gene transcription. Multiple biological processes have been suggested to be tightly related to the dynamics of H2B monoubiquitination. However, a comprehensive understanding of biological roles of H2B monoubiquitination is still poorly understood. In the present study, we developed an efficient tool to disrupt endogenous H2B monoubiquitination levels by using an H2BK120R mutant construct expressed in human cells. Genome-wide microarray analysis of these cells revealed a potential global view of biological functions of H2B monoubiquitination. Bioinformatics analysis of our data demonstrated that while H2B monoubiquitination expectedly affected a number of previously reported biological pathways, we also uncovered the influence of this histone modification on many novel biological processes. Therefore, our work provided valuable information for understanding the role of H2B monoubiquitination and indicated potential directions for its further studies. |
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Multiple biological processes have been suggested to be tightly related to the dynamics of H2B monoubiquitination. However, a comprehensive understanding of biological roles of H2B monoubiquitination is still poorly understood. In the present study, we developed an efficient tool to disrupt endogenous H2B monoubiquitination levels by using an H2BK120R mutant construct expressed in human cells. Genome-wide microarray analysis of these cells revealed a potential global view of biological functions of H2B monoubiquitination. Bioinformatics analysis of our data demonstrated that while H2B monoubiquitination expectedly affected a number of previously reported biological pathways, we also uncovered the influence of this histone modification on many novel biological processes. Therefore, our work provided valuable information for understanding the role of H2B monoubiquitination and indicated potential directions for its further studies.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0133444</identifier><identifier>PMID: 26177367</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Bioinformatics ; Biological activity ; Biological effects ; Breast cancer ; Cell cycle ; Cell Differentiation - genetics ; Chromatin ; Chromatin - metabolism ; Data processing ; Deoxyribonucleic acid ; DNA ; DNA Damage - genetics ; DNA methylation ; DNA microarrays ; DNA Repair - genetics ; Education ; Gene Expression Profiling ; Gene Expression Regulation ; Gene Knockdown Techniques ; Genes ; Genomes ; HEK293 Cells ; HeLa Cells ; Histone H2B ; Histones - genetics ; Histones - metabolism ; Humans ; Life sciences ; Mammals ; Medicine ; Mice ; Mouse Embryonic Stem Cells - cytology ; Mutant Proteins - metabolism ; Mutation - genetics ; Oligonucleotide Array Sequence Analysis ; Stem cells ; Surgery ; Transcription ; Tumorigenesis ; Ubiquitin - metabolism ; Ubiquitination</subject><ispartof>PloS one, 2015-07, Vol.10 (7), p.e0133444-e0133444</ispartof><rights>2015 Wu et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Wu et al 2015 Wu et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-7fea30f495c12f72abea9235ae811e72645a6f6004a83eb12a569f54aa5544623</citedby><cites>FETCH-LOGICAL-c526t-7fea30f495c12f72abea9235ae811e72645a6f6004a83eb12a569f54aa5544623</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1696687427/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1696687427?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26177367$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Mantovani, Roberto</contributor><creatorcontrib>Wu, You</creatorcontrib><creatorcontrib>Chen, Ping</creatorcontrib><creatorcontrib>Jing, Yuanya</creatorcontrib><creatorcontrib>Wang, Chen</creatorcontrib><creatorcontrib>Men, Yu-Long</creatorcontrib><creatorcontrib>Zhan, Wang</creatorcontrib><creatorcontrib>Wang, Qiang</creatorcontrib><creatorcontrib>Gan, Zhixue</creatorcontrib><creatorcontrib>Huang, Jin</creatorcontrib><creatorcontrib>Xie, Kun</creatorcontrib><creatorcontrib>Mi, Jiangsheng</creatorcontrib><creatorcontrib>Yu, Chenghua</creatorcontrib><creatorcontrib>Yu, Xiuqing</creatorcontrib><creatorcontrib>Chen, Pei-Chao</creatorcontrib><creatorcontrib>Chang, Jian-Feng</creatorcontrib><creatorcontrib>Cai, Fengfeng</creatorcontrib><creatorcontrib>Chen, Su</creatorcontrib><title>Microarray Analysis Reveals Potential Biological Functions of Histone H2B Monoubiquitination</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Histone H2B monoubiquitination is a key histone modification that has significant effects on chromatin higher-order structure and gene transcription. Multiple biological processes have been suggested to be tightly related to the dynamics of H2B monoubiquitination. However, a comprehensive understanding of biological roles of H2B monoubiquitination is still poorly understood. In the present study, we developed an efficient tool to disrupt endogenous H2B monoubiquitination levels by using an H2BK120R mutant construct expressed in human cells. Genome-wide microarray analysis of these cells revealed a potential global view of biological functions of H2B monoubiquitination. Bioinformatics analysis of our data demonstrated that while H2B monoubiquitination expectedly affected a number of previously reported biological pathways, we also uncovered the influence of this histone modification on many novel biological processes. Therefore, our work provided valuable information for understanding the role of H2B monoubiquitination and indicated potential directions for its further studies.</description><subject>Animals</subject><subject>Bioinformatics</subject><subject>Biological activity</subject><subject>Biological effects</subject><subject>Breast cancer</subject><subject>Cell cycle</subject><subject>Cell Differentiation - genetics</subject><subject>Chromatin</subject><subject>Chromatin - metabolism</subject><subject>Data processing</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA Damage - genetics</subject><subject>DNA methylation</subject><subject>DNA microarrays</subject><subject>DNA Repair - genetics</subject><subject>Education</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation</subject><subject>Gene Knockdown Techniques</subject><subject>Genes</subject><subject>Genomes</subject><subject>HEK293 Cells</subject><subject>HeLa Cells</subject><subject>Histone H2B</subject><subject>Histones - genetics</subject><subject>Histones - metabolism</subject><subject>Humans</subject><subject>Life sciences</subject><subject>Mammals</subject><subject>Medicine</subject><subject>Mice</subject><subject>Mouse Embryonic Stem Cells - cytology</subject><subject>Mutant Proteins - metabolism</subject><subject>Mutation - genetics</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Stem cells</subject><subject>Surgery</subject><subject>Transcription</subject><subject>Tumorigenesis</subject><subject>Ubiquitin - metabolism</subject><subject>Ubiquitination</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkl1rFDEUhoMotlb_geiAN97smu9kboS2WLfQoojeCeFMNlmzZCfbZKaw_95sd1pa8SqH5D3P-ciL0FuC54Qp8mmdxtxDnG9T7-aYMMY5f4aOScvoTFLMnj-Kj9CrUtYYC6alfImOqCRKMamO0e_rYHOCnGHXnFbcroTS_HC3DmJpvqfB9UOA2JyFFNMq2BpejL0dQupLk3yzCGWo9ZsFPWuuU5_GLtyMYQg97CWv0QtfOe7NdJ6gXxdffp4vZlffvl6en17NrKBymCnvgGHPW2EJ9YpC56ClTIDThDhFJRcgvcSYg2auIxSEbL3gAEJwLik7Qe8P3G1MxUyLKYbIVkqtOFVVcXlQLBOszTaHDeSdSRDM3UXKKwN5CDY60ynPtNLOOr_kmDHgngis5bLlQoDWlfV5qjZ2G7e0dUUZ4hPo05c-_DGrdGu4qDjBK-DjBMjpZnRlMJtQrIsRepfGu76VEoLxtko__CP9_3T8oKpfWUp2_qEZgs3eLPdZZm8WM5mlpr17PMhD0r072F-HF727</recordid><startdate>20150715</startdate><enddate>20150715</enddate><creator>Wu, You</creator><creator>Chen, Ping</creator><creator>Jing, Yuanya</creator><creator>Wang, Chen</creator><creator>Men, Yu-Long</creator><creator>Zhan, Wang</creator><creator>Wang, Qiang</creator><creator>Gan, Zhixue</creator><creator>Huang, Jin</creator><creator>Xie, Kun</creator><creator>Mi, Jiangsheng</creator><creator>Yu, Chenghua</creator><creator>Yu, Xiuqing</creator><creator>Chen, Pei-Chao</creator><creator>Chang, Jian-Feng</creator><creator>Cai, Fengfeng</creator><creator>Chen, Su</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><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>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20150715</creationdate><title>Microarray Analysis Reveals Potential Biological Functions of Histone H2B Monoubiquitination</title><author>Wu, You ; Chen, Ping ; Jing, Yuanya ; Wang, Chen ; Men, Yu-Long ; Zhan, Wang ; Wang, Qiang ; Gan, Zhixue ; Huang, Jin ; Xie, Kun ; Mi, Jiangsheng ; Yu, Chenghua ; Yu, Xiuqing ; Chen, Pei-Chao ; Chang, Jian-Feng ; Cai, Fengfeng ; Chen, Su</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c526t-7fea30f495c12f72abea9235ae811e72645a6f6004a83eb12a569f54aa5544623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Bioinformatics</topic><topic>Biological activity</topic><topic>Biological effects</topic><topic>Breast cancer</topic><topic>Cell cycle</topic><topic>Cell Differentiation - 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Multiple biological processes have been suggested to be tightly related to the dynamics of H2B monoubiquitination. However, a comprehensive understanding of biological roles of H2B monoubiquitination is still poorly understood. In the present study, we developed an efficient tool to disrupt endogenous H2B monoubiquitination levels by using an H2BK120R mutant construct expressed in human cells. Genome-wide microarray analysis of these cells revealed a potential global view of biological functions of H2B monoubiquitination. Bioinformatics analysis of our data demonstrated that while H2B monoubiquitination expectedly affected a number of previously reported biological pathways, we also uncovered the influence of this histone modification on many novel biological processes. Therefore, our work provided valuable information for understanding the role of H2B monoubiquitination and indicated potential directions for its further studies.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26177367</pmid><doi>10.1371/journal.pone.0133444</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animals Bioinformatics Biological activity Biological effects Breast cancer Cell cycle Cell Differentiation - genetics Chromatin Chromatin - metabolism Data processing Deoxyribonucleic acid DNA DNA Damage - genetics DNA methylation DNA microarrays DNA Repair - genetics Education Gene Expression Profiling Gene Expression Regulation Gene Knockdown Techniques Genes Genomes HEK293 Cells HeLa Cells Histone H2B Histones - genetics Histones - metabolism Humans Life sciences Mammals Medicine Mice Mouse Embryonic Stem Cells - cytology Mutant Proteins - metabolism Mutation - genetics Oligonucleotide Array Sequence Analysis Stem cells Surgery Transcription Tumorigenesis Ubiquitin - metabolism Ubiquitination |
title | Microarray Analysis Reveals Potential Biological Functions of Histone H2B Monoubiquitination |
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