Roles of Brahma and Brahma/SWI2-Related Gene 1 in Hypoxic Induction of the Erythropoietin Gene
Upon hypoxia, the human erythropoietin ( EPO ) gene is transactivated by the heterodimeric hypoxia-inducible factor 1 (HIF-1). Mammalian SWI/SNF is a chromatin-remodeling complex involved in the modulation of gene expression. We demonstrate that Brahma (Brm) and Brahma/SWI2-related gene 1 (Brg-1), a...
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creator | Wang, Feng Zhang, Ruixue Beischlag, Timothy V Muchardt, Christian Yaniv, Moshe Hankinson, Oliver |
description | Upon hypoxia, the human erythropoietin ( EPO ) gene is transactivated by the heterodimeric hypoxia-inducible factor 1 (HIF-1). Mammalian SWI/SNF is a chromatin-remodeling
complex involved in the modulation of gene expression. We demonstrate that Brahma (Brm) and Brahma/SWI2-related gene 1 (Brg-1),
alternative ATPase subunits of SWI/SNF, potentiate reporter gene activation mediated by HIF-1 in an ATPase-dependent manner.
Brm was more potent than Brg-1 in the reporter gene assays. Simultaneous depletion of both Brm and Brg-1 by small interfering
RNAs significantly compromised the transcription of the endogenous EPO gene triggered by hypoxia. Whereas knocking down Brm alone resulted in a moderate reduction in transcription of the EPO gene, depletion of Brg-1 resulted in an augmentation of transcription of both the EPO gene and the Brm gene, indicating that Brm can compensate for loss of Brg-1. Chromatin immunoprecipitation (ChIP) and sequential ChIP (re-ChIP)
analysis showed that both Brm and Brg-1 associate with the enhancer region of the EPO gene in vivo in a hypoxia-dependent fashion and that each is present in a complex with HIF-1. Brm and Brg-1 were also recruited to the
promoter of the vascular endothelial growth factor ( VEGF ) gene in a hypoxia-dependent fashion, although hypoxic induction of VEGF transcription was not affected by depletions of either or both Brm and Brg-1. Together these studies reveal a novel role
for SWI/SNF in the activation of transcription of the EPO gene, indicate an important communication and compensation between Brm and Brg-1, and suggest that the requirement for SWI/SNF
during hypoxic induction is gene-specific. |
doi_str_mv | 10.1074/jbc.M409002200 |
format | Article |
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complex involved in the modulation of gene expression. We demonstrate that Brahma (Brm) and Brahma/SWI2-related gene 1 (Brg-1),
alternative ATPase subunits of SWI/SNF, potentiate reporter gene activation mediated by HIF-1 in an ATPase-dependent manner.
Brm was more potent than Brg-1 in the reporter gene assays. Simultaneous depletion of both Brm and Brg-1 by small interfering
RNAs significantly compromised the transcription of the endogenous EPO gene triggered by hypoxia. Whereas knocking down Brm alone resulted in a moderate reduction in transcription of the EPO gene, depletion of Brg-1 resulted in an augmentation of transcription of both the EPO gene and the Brm gene, indicating that Brm can compensate for loss of Brg-1. Chromatin immunoprecipitation (ChIP) and sequential ChIP (re-ChIP)
analysis showed that both Brm and Brg-1 associate with the enhancer region of the EPO gene in vivo in a hypoxia-dependent fashion and that each is present in a complex with HIF-1. Brm and Brg-1 were also recruited to the
promoter of the vascular endothelial growth factor ( VEGF ) gene in a hypoxia-dependent fashion, although hypoxic induction of VEGF transcription was not affected by depletions of either or both Brm and Brg-1. Together these studies reveal a novel role
for SWI/SNF in the activation of transcription of the EPO gene, indicate an important communication and compensation between Brm and Brg-1, and suggest that the requirement for SWI/SNF
during hypoxic induction is gene-specific.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M409002200</identifier><identifier>PMID: 15347669</identifier><language>eng</language><publisher>United States: American Society for Biochemistry and Molecular Biology</publisher><subject>3' Untranslated Regions ; Cell Cycle Proteins - metabolism ; Cell Cycle Proteins - physiology ; Cell Line ; Cell Line, Tumor ; Chromatin - metabolism ; Cross-Linking Reagents - pharmacology ; Dimerization ; DNA Helicases ; Drosophila Proteins ; Enhancer Elements, Genetic ; Erythropoietin - biosynthesis ; Erythropoietin - genetics ; Genes, Reporter ; Genetic Vectors ; Histones - chemistry ; Histones - metabolism ; Humans ; Hypoxia ; Immunoprecipitation ; Luciferases - metabolism ; Models, Genetic ; Nuclear Proteins - metabolism ; Nuclear Proteins - physiology ; Oxygen - metabolism ; Plasmids - metabolism ; Reverse Transcriptase Polymerase Chain Reaction ; RNA Interference ; RNA, Small Interfering - metabolism ; Trans-Activators - metabolism ; Trans-Activators - physiology ; Transcription Factors - metabolism ; Transcription Factors - physiology ; Transcription, Genetic ; Transcriptional Activation ; Transfection ; Vascular Endothelial Growth Factor A - metabolism</subject><ispartof>The Journal of biological chemistry, 2004-11, Vol.279 (45), p.46733-46741</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c457t-ef45a4c21700e9362ccb9f9b1dd6ab7e316569a78fd3352c8dd0768292809fcd3</citedby><cites>FETCH-LOGICAL-c457t-ef45a4c21700e9362ccb9f9b1dd6ab7e316569a78fd3352c8dd0768292809fcd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15347669$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Feng</creatorcontrib><creatorcontrib>Zhang, Ruixue</creatorcontrib><creatorcontrib>Beischlag, Timothy V</creatorcontrib><creatorcontrib>Muchardt, Christian</creatorcontrib><creatorcontrib>Yaniv, Moshe</creatorcontrib><creatorcontrib>Hankinson, Oliver</creatorcontrib><title>Roles of Brahma and Brahma/SWI2-Related Gene 1 in Hypoxic Induction of the Erythropoietin Gene</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Upon hypoxia, the human erythropoietin ( EPO ) gene is transactivated by the heterodimeric hypoxia-inducible factor 1 (HIF-1). Mammalian SWI/SNF is a chromatin-remodeling
complex involved in the modulation of gene expression. We demonstrate that Brahma (Brm) and Brahma/SWI2-related gene 1 (Brg-1),
alternative ATPase subunits of SWI/SNF, potentiate reporter gene activation mediated by HIF-1 in an ATPase-dependent manner.
Brm was more potent than Brg-1 in the reporter gene assays. Simultaneous depletion of both Brm and Brg-1 by small interfering
RNAs significantly compromised the transcription of the endogenous EPO gene triggered by hypoxia. Whereas knocking down Brm alone resulted in a moderate reduction in transcription of the EPO gene, depletion of Brg-1 resulted in an augmentation of transcription of both the EPO gene and the Brm gene, indicating that Brm can compensate for loss of Brg-1. Chromatin immunoprecipitation (ChIP) and sequential ChIP (re-ChIP)
analysis showed that both Brm and Brg-1 associate with the enhancer region of the EPO gene in vivo in a hypoxia-dependent fashion and that each is present in a complex with HIF-1. Brm and Brg-1 were also recruited to the
promoter of the vascular endothelial growth factor ( VEGF ) gene in a hypoxia-dependent fashion, although hypoxic induction of VEGF transcription was not affected by depletions of either or both Brm and Brg-1. Together these studies reveal a novel role
for SWI/SNF in the activation of transcription of the EPO gene, indicate an important communication and compensation between Brm and Brg-1, and suggest that the requirement for SWI/SNF
during hypoxic induction is gene-specific.</description><subject>3' Untranslated Regions</subject><subject>Cell Cycle Proteins - metabolism</subject><subject>Cell Cycle Proteins - physiology</subject><subject>Cell Line</subject><subject>Cell Line, Tumor</subject><subject>Chromatin - metabolism</subject><subject>Cross-Linking Reagents - pharmacology</subject><subject>Dimerization</subject><subject>DNA Helicases</subject><subject>Drosophila Proteins</subject><subject>Enhancer Elements, Genetic</subject><subject>Erythropoietin - biosynthesis</subject><subject>Erythropoietin - genetics</subject><subject>Genes, Reporter</subject><subject>Genetic Vectors</subject><subject>Histones - chemistry</subject><subject>Histones - metabolism</subject><subject>Humans</subject><subject>Hypoxia</subject><subject>Immunoprecipitation</subject><subject>Luciferases - metabolism</subject><subject>Models, Genetic</subject><subject>Nuclear Proteins - metabolism</subject><subject>Nuclear Proteins - physiology</subject><subject>Oxygen - metabolism</subject><subject>Plasmids - metabolism</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA Interference</subject><subject>RNA, Small Interfering - metabolism</subject><subject>Trans-Activators - metabolism</subject><subject>Trans-Activators - physiology</subject><subject>Transcription Factors - metabolism</subject><subject>Transcription Factors - physiology</subject><subject>Transcription, Genetic</subject><subject>Transcriptional Activation</subject><subject>Transfection</subject><subject>Vascular Endothelial Growth Factor A - metabolism</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkD1v2zAQhokiQeO4XTsGHIJucvglUhzbIB8GUhRwGyRTCIo8RQwk0SVlJP73kWEDGXvLHQ7P-w4PQt8oWVCixMVL7Ra_BNGEMEbIJzSjpOIFL-njEZpNT1poVlYn6DTnFzKN0PQzOqElF0pKPUNPq9hBxrHBP5Nte4vt4A_nxZ-HJStW0NkRPL6BATDFYcC323V8Cw4vB79xY4jDLj22gK_SdmxTXMcA48TtEl_QcWO7DF8Pe47ur6_-Xt4Wd79vlpc_7gonSjUW0IjSCseoIgQ0l8y5Wje6pt5LWyvgVJZSW1U1nvOSucp7omTFNKuIbpznc_R937tO8d8G8mj6kB10nR0gbrKRijBJlfgvSJXSlCs6gYs96FLMOUFj1in0Nm0NJWan3kzqzYf6KXB2aN7UPfgP_OB6As73QBue29eQwNQhuhZ6w5Q2ojRCKs75O3cniXo</recordid><startdate>20041105</startdate><enddate>20041105</enddate><creator>Wang, Feng</creator><creator>Zhang, Ruixue</creator><creator>Beischlag, Timothy V</creator><creator>Muchardt, Christian</creator><creator>Yaniv, Moshe</creator><creator>Hankinson, Oliver</creator><general>American Society for Biochemistry and Molecular Biology</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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20041105</creationdate><title>Roles of Brahma and Brahma/SWI2-Related Gene 1 in Hypoxic Induction of the Erythropoietin Gene</title><author>Wang, Feng ; Zhang, Ruixue ; Beischlag, Timothy V ; Muchardt, Christian ; Yaniv, Moshe ; Hankinson, Oliver</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c457t-ef45a4c21700e9362ccb9f9b1dd6ab7e316569a78fd3352c8dd0768292809fcd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>3' Untranslated Regions</topic><topic>Cell Cycle Proteins - metabolism</topic><topic>Cell Cycle Proteins - physiology</topic><topic>Cell Line</topic><topic>Cell Line, Tumor</topic><topic>Chromatin - metabolism</topic><topic>Cross-Linking Reagents - pharmacology</topic><topic>Dimerization</topic><topic>DNA Helicases</topic><topic>Drosophila Proteins</topic><topic>Enhancer Elements, Genetic</topic><topic>Erythropoietin - biosynthesis</topic><topic>Erythropoietin - genetics</topic><topic>Genes, Reporter</topic><topic>Genetic Vectors</topic><topic>Histones - chemistry</topic><topic>Histones - metabolism</topic><topic>Humans</topic><topic>Hypoxia</topic><topic>Immunoprecipitation</topic><topic>Luciferases - metabolism</topic><topic>Models, Genetic</topic><topic>Nuclear Proteins - metabolism</topic><topic>Nuclear Proteins - physiology</topic><topic>Oxygen - metabolism</topic><topic>Plasmids - metabolism</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA Interference</topic><topic>RNA, Small Interfering - metabolism</topic><topic>Trans-Activators - metabolism</topic><topic>Trans-Activators - physiology</topic><topic>Transcription Factors - metabolism</topic><topic>Transcription Factors - physiology</topic><topic>Transcription, Genetic</topic><topic>Transcriptional Activation</topic><topic>Transfection</topic><topic>Vascular Endothelial Growth Factor A - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Feng</creatorcontrib><creatorcontrib>Zhang, Ruixue</creatorcontrib><creatorcontrib>Beischlag, Timothy V</creatorcontrib><creatorcontrib>Muchardt, Christian</creatorcontrib><creatorcontrib>Yaniv, Moshe</creatorcontrib><creatorcontrib>Hankinson, Oliver</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Feng</au><au>Zhang, Ruixue</au><au>Beischlag, Timothy V</au><au>Muchardt, Christian</au><au>Yaniv, Moshe</au><au>Hankinson, Oliver</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Roles of Brahma and Brahma/SWI2-Related Gene 1 in Hypoxic Induction of the Erythropoietin Gene</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2004-11-05</date><risdate>2004</risdate><volume>279</volume><issue>45</issue><spage>46733</spage><epage>46741</epage><pages>46733-46741</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Upon hypoxia, the human erythropoietin ( EPO ) gene is transactivated by the heterodimeric hypoxia-inducible factor 1 (HIF-1). Mammalian SWI/SNF is a chromatin-remodeling
complex involved in the modulation of gene expression. We demonstrate that Brahma (Brm) and Brahma/SWI2-related gene 1 (Brg-1),
alternative ATPase subunits of SWI/SNF, potentiate reporter gene activation mediated by HIF-1 in an ATPase-dependent manner.
Brm was more potent than Brg-1 in the reporter gene assays. Simultaneous depletion of both Brm and Brg-1 by small interfering
RNAs significantly compromised the transcription of the endogenous EPO gene triggered by hypoxia. Whereas knocking down Brm alone resulted in a moderate reduction in transcription of the EPO gene, depletion of Brg-1 resulted in an augmentation of transcription of both the EPO gene and the Brm gene, indicating that Brm can compensate for loss of Brg-1. Chromatin immunoprecipitation (ChIP) and sequential ChIP (re-ChIP)
analysis showed that both Brm and Brg-1 associate with the enhancer region of the EPO gene in vivo in a hypoxia-dependent fashion and that each is present in a complex with HIF-1. Brm and Brg-1 were also recruited to the
promoter of the vascular endothelial growth factor ( VEGF ) gene in a hypoxia-dependent fashion, although hypoxic induction of VEGF transcription was not affected by depletions of either or both Brm and Brg-1. Together these studies reveal a novel role
for SWI/SNF in the activation of transcription of the EPO gene, indicate an important communication and compensation between Brm and Brg-1, and suggest that the requirement for SWI/SNF
during hypoxic induction is gene-specific.</abstract><cop>United States</cop><pub>American Society for Biochemistry and Molecular Biology</pub><pmid>15347669</pmid><doi>10.1074/jbc.M409002200</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | 3' Untranslated Regions Cell Cycle Proteins - metabolism Cell Cycle Proteins - physiology Cell Line Cell Line, Tumor Chromatin - metabolism Cross-Linking Reagents - pharmacology Dimerization DNA Helicases Drosophila Proteins Enhancer Elements, Genetic Erythropoietin - biosynthesis Erythropoietin - genetics Genes, Reporter Genetic Vectors Histones - chemistry Histones - metabolism Humans Hypoxia Immunoprecipitation Luciferases - metabolism Models, Genetic Nuclear Proteins - metabolism Nuclear Proteins - physiology Oxygen - metabolism Plasmids - metabolism Reverse Transcriptase Polymerase Chain Reaction RNA Interference RNA, Small Interfering - metabolism Trans-Activators - metabolism Trans-Activators - physiology Transcription Factors - metabolism Transcription Factors - physiology Transcription, Genetic Transcriptional Activation Transfection Vascular Endothelial Growth Factor A - metabolism |
title | Roles of Brahma and Brahma/SWI2-Related Gene 1 in Hypoxic Induction of the Erythropoietin Gene |
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