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Upstream Stimulatory Factor 2 Activates the Mammalian F1F0 ATP Synthase α-Subunit Gene Through an Initiator Element
The F1F0 ATP synthase is the central enzyme complex of the mitochondrial oxidative phosphorylation system synthesizing ATP from ADP and Pi. Our laboratory has been studying the transcriptional regulation of the nuclear gene that encodes the α-subunit of the mammalian mitochondrial ATP synthase compl...
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Published in: | Gene expression 1998-01, Vol.7 (3), p.163-170 |
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creator | BREEN, GAIL A. M. JORDAN, ELZORA M. |
description | The F1F0 ATP synthase is the central enzyme complex of the mitochondrial oxidative phosphorylation system synthesizing ATP from ADP and Pi. Our laboratory has been studying the transcriptional regulation of the nuclear gene that encodes the α-subunit
of the mammalian mitochondrial ATP synthase complex (ATPA). We have previously identified an initiator element in the core promoter that plays an important role in expression of this gene. In this article, we demonstrate that ectopic expression of the transcription factor, upstream
stimulatory factor 2 (USF2), transactivates the ATPA gene through this initiator element. Importantly, cotransfection of a dominant-negative USF2 mutant significantly reduces both the basal activity and the level of activation of the ATPA initiator by coexpressed USF2 demonstrating
the role of endogenous USF2 proteins in this activation. We also identify several nucleotides in the ATPA initiator element that are important for both basal activity and USF2-dependent transactivation. We have also previously determined that the binding of the multifunctional regulatory
protein, YY1, to this initiator element can positively regulate the ATPA gene. Here, we show that expression of YY1 together with USF2 results in a decreased level of activation of the ATPA initiator relative to expression of USF2 alone, suggesting competition between these two
regulatory proteins. |
format | article |
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of the mammalian mitochondrial ATP synthase complex (ATPA). We have previously identified an initiator element in the core promoter that plays an important role in expression of this gene. In this article, we demonstrate that ectopic expression of the transcription factor, upstream
stimulatory factor 2 (USF2), transactivates the ATPA gene through this initiator element. Importantly, cotransfection of a dominant-negative USF2 mutant significantly reduces both the basal activity and the level of activation of the ATPA initiator by coexpressed USF2 demonstrating
the role of endogenous USF2 proteins in this activation. We also identify several nucleotides in the ATPA initiator element that are important for both basal activity and USF2-dependent transactivation. We have also previously determined that the binding of the multifunctional regulatory
protein, YY1, to this initiator element can positively regulate the ATPA gene. Here, we show that expression of YY1 together with USF2 results in a decreased level of activation of the ATPA initiator relative to expression of USF2 alone, suggesting competition between these two
regulatory proteins.</description><identifier>ISSN: 1052-2166</identifier><identifier>EISSN: 1555-3884</identifier><identifier>PMID: 9840809</identifier><language>eng</language><publisher>Elmsford, NY: Cognizant Communication Corporation</publisher><subject>Animals ; Atp Synthase ; Atpa Gene ; Base Sequence ; DNA-Binding Proteins - genetics ; DNA-Binding Proteins - metabolism ; Erythroid-Specific DNA-Binding Factors ; Genes, Dominant ; Humans ; Initiator Element ; Mammals ; Molecular Sequence Data ; Mutation ; Promoter Regions, Genetic ; Proton-Translocating ATPases - genetics ; Proton-Translocating ATPases - metabolism ; Regulatory Sequences, Nucleic Acid ; Trans-Activators - genetics ; Trans-Activators - metabolism ; Transcription Factors - genetics ; Transcription Factors - metabolism ; Upstream Stimulatory Factor 2 ; Upstream Stimulatory Factors ; YY1 Transcription Factor</subject><ispartof>Gene expression, 1998-01, Vol.7 (3), p.163-170</ispartof><rights>Copyright © 1998 Cognizant Comm. Corp. 1998</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151952/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151952/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9840809$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>BREEN, GAIL A. M.</creatorcontrib><creatorcontrib>JORDAN, ELZORA M.</creatorcontrib><title>Upstream Stimulatory Factor 2 Activates the Mammalian F1F0 ATP Synthase α-Subunit Gene Through an Initiator Element</title><title>Gene expression</title><addtitle>Gene Expr</addtitle><description>The F1F0 ATP synthase is the central enzyme complex of the mitochondrial oxidative phosphorylation system synthesizing ATP from ADP and Pi. Our laboratory has been studying the transcriptional regulation of the nuclear gene that encodes the α-subunit
of the mammalian mitochondrial ATP synthase complex (ATPA). We have previously identified an initiator element in the core promoter that plays an important role in expression of this gene. In this article, we demonstrate that ectopic expression of the transcription factor, upstream
stimulatory factor 2 (USF2), transactivates the ATPA gene through this initiator element. Importantly, cotransfection of a dominant-negative USF2 mutant significantly reduces both the basal activity and the level of activation of the ATPA initiator by coexpressed USF2 demonstrating
the role of endogenous USF2 proteins in this activation. We also identify several nucleotides in the ATPA initiator element that are important for both basal activity and USF2-dependent transactivation. We have also previously determined that the binding of the multifunctional regulatory
protein, YY1, to this initiator element can positively regulate the ATPA gene. Here, we show that expression of YY1 together with USF2 results in a decreased level of activation of the ATPA initiator relative to expression of USF2 alone, suggesting competition between these two
regulatory proteins.</description><subject>Animals</subject><subject>Atp Synthase</subject><subject>Atpa Gene</subject><subject>Base Sequence</subject><subject>DNA-Binding Proteins - genetics</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Erythroid-Specific DNA-Binding Factors</subject><subject>Genes, Dominant</subject><subject>Humans</subject><subject>Initiator Element</subject><subject>Mammals</subject><subject>Molecular Sequence Data</subject><subject>Mutation</subject><subject>Promoter Regions, Genetic</subject><subject>Proton-Translocating ATPases - genetics</subject><subject>Proton-Translocating ATPases - metabolism</subject><subject>Regulatory Sequences, Nucleic Acid</subject><subject>Trans-Activators - genetics</subject><subject>Trans-Activators - metabolism</subject><subject>Transcription Factors - genetics</subject><subject>Transcription Factors - metabolism</subject><subject>Upstream Stimulatory Factor 2</subject><subject>Upstream Stimulatory Factors</subject><subject>YY1 Transcription Factor</subject><issn>1052-2166</issn><issn>1555-3884</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNpVkNFq2zAUhs1Y6bK0j1DQ1e4MkhzZ0s0ghKYNZGyQ9FocK8e2ii1nklzIY_VF-kzT1qxbz83_c3TO_0n6kM2YECIvpFx8TJ4KnnNWlp-yzyE8Usqpkvwyu1RyQSVVsyw-HEP0CAPZRTtMPcTRn8gaTFLCydJE-wQRA4kdkm8wDNBbcGTN1pQs9z_I7uRiBwHJy3O-m-rJ2Uju0CHZd36c2o6k4U1q2t_B5LbHAV28yi4a6ANen3WePaxv96v7fPv9brNabnNbsDLmCitZ1UYAUiGaolpwNIbVCg6UNozWTSMlgwMavuCsohTK5pAWS1HWDSjGinn29TX3ONUDHkxCe-j10dsB_EmPYPX7E2c73Y5PumSCKcFTwJdzgB9_ThiiHmww2PfgcJyCTlDJilTz7OZ_0hvi_M__bmJdm1igH8fJu_R2bcZWt6iZUlLT16r-mkKDj39M8Qtgk5Ah</recordid><startdate>19980101</startdate><enddate>19980101</enddate><creator>BREEN, GAIL A. M.</creator><creator>JORDAN, ELZORA M.</creator><general>Cognizant Communication Corporation</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19980101</creationdate><title>Upstream Stimulatory Factor 2 Activates the Mammalian F1F0 ATP Synthase α-Subunit Gene Through an Initiator Element</title><author>BREEN, GAIL A. M. ; JORDAN, ELZORA M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i316t-9e787bc5ae055f3742ecc1b9ad00f10bff881adec2421700a6fd316656bfa9113</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Atp Synthase</topic><topic>Atpa Gene</topic><topic>Base Sequence</topic><topic>DNA-Binding Proteins - genetics</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Erythroid-Specific DNA-Binding Factors</topic><topic>Genes, Dominant</topic><topic>Humans</topic><topic>Initiator Element</topic><topic>Mammals</topic><topic>Molecular Sequence Data</topic><topic>Mutation</topic><topic>Promoter Regions, Genetic</topic><topic>Proton-Translocating ATPases - genetics</topic><topic>Proton-Translocating ATPases - metabolism</topic><topic>Regulatory Sequences, Nucleic Acid</topic><topic>Trans-Activators - genetics</topic><topic>Trans-Activators - metabolism</topic><topic>Transcription Factors - genetics</topic><topic>Transcription Factors - metabolism</topic><topic>Upstream Stimulatory Factor 2</topic><topic>Upstream Stimulatory Factors</topic><topic>YY1 Transcription Factor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BREEN, GAIL A. M.</creatorcontrib><creatorcontrib>JORDAN, ELZORA M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Gene expression</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>BREEN, GAIL A. M.</au><au>JORDAN, ELZORA M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Upstream Stimulatory Factor 2 Activates the Mammalian F1F0 ATP Synthase α-Subunit Gene Through an Initiator Element</atitle><jtitle>Gene expression</jtitle><addtitle>Gene Expr</addtitle><date>1998-01-01</date><risdate>1998</risdate><volume>7</volume><issue>3</issue><spage>163</spage><epage>170</epage><pages>163-170</pages><issn>1052-2166</issn><eissn>1555-3884</eissn><abstract>The F1F0 ATP synthase is the central enzyme complex of the mitochondrial oxidative phosphorylation system synthesizing ATP from ADP and Pi. Our laboratory has been studying the transcriptional regulation of the nuclear gene that encodes the α-subunit
of the mammalian mitochondrial ATP synthase complex (ATPA). We have previously identified an initiator element in the core promoter that plays an important role in expression of this gene. In this article, we demonstrate that ectopic expression of the transcription factor, upstream
stimulatory factor 2 (USF2), transactivates the ATPA gene through this initiator element. Importantly, cotransfection of a dominant-negative USF2 mutant significantly reduces both the basal activity and the level of activation of the ATPA initiator by coexpressed USF2 demonstrating
the role of endogenous USF2 proteins in this activation. We also identify several nucleotides in the ATPA initiator element that are important for both basal activity and USF2-dependent transactivation. We have also previously determined that the binding of the multifunctional regulatory
protein, YY1, to this initiator element can positively regulate the ATPA gene. Here, we show that expression of YY1 together with USF2 results in a decreased level of activation of the ATPA initiator relative to expression of USF2 alone, suggesting competition between these two
regulatory proteins.</abstract><cop>Elmsford, NY</cop><pub>Cognizant Communication Corporation</pub><pmid>9840809</pmid><tpages>8</tpages></addata></record> |
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subjects | Animals Atp Synthase Atpa Gene Base Sequence DNA-Binding Proteins - genetics DNA-Binding Proteins - metabolism Erythroid-Specific DNA-Binding Factors Genes, Dominant Humans Initiator Element Mammals Molecular Sequence Data Mutation Promoter Regions, Genetic Proton-Translocating ATPases - genetics Proton-Translocating ATPases - metabolism Regulatory Sequences, Nucleic Acid Trans-Activators - genetics Trans-Activators - metabolism Transcription Factors - genetics Transcription Factors - metabolism Upstream Stimulatory Factor 2 Upstream Stimulatory Factors YY1 Transcription Factor |
title | Upstream Stimulatory Factor 2 Activates the Mammalian F1F0 ATP Synthase α-Subunit Gene Through an Initiator Element |
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