Expression of SRG3, a core component of mouse SWI/SNF chromatin-remodeling complex, is regulated by cooperative interactions between Sp1/Sp3 and Ets transcription factors
SRG3, a mouse homolog of yeast SWI3 and human BAF155, is known to be a core component of SWI/SNF chromatin-remodeling complex. We have previously shown that SRG3 plays essential roles in early mouse embryogenesis, brain development, and T-cell development. SRG3 gene expression was differentially reg...
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Veröffentlicht in: | Biochemical and biophysical research communications 2005-12, Vol.338 (3), p.1435-1446 |
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creator | Ahn, Jeongeun Ko, Myunggon Lee, Kyuyoung Oh, Jaehak Jeon, Sung H. Seong, Rho H. |
description | SRG3, a mouse homolog of yeast SWI3 and human BAF155, is known to be a core component of SWI/SNF chromatin-remodeling complex. We have previously shown that SRG3 plays essential roles in early mouse embryogenesis, brain development, and T-cell development. SRG3 gene expression was differentially regulated depending on the developmental stages and exhibited tissue-specific pattern. In this study, we showed that the functional interactions between Sp and Ets family transcription factors are crucial for the SRG3 expression. Sp1 and Sp3 specifically bound to the two canonical Sp-binding sites (GC boxes) at −152 and −114, and a non-canonical Sp-binding site (CCTCCT motif) at −108 in the SRG3 promoter. Using
Drosophila SL2 cells, we found that various Sp or Ets family members activate the SRG3 promoter through these Sp- or Ets-binding sites, respectively, in a dose-dependent manner. Intriguingly, different combinatorial expression of Ets and Sp factors in SL2 cells resulted in either strong synergistic activation or repression of the SRG3 promoter activity. Moreover, the Sp-mediated activation of SRG3 promoter required the intact Ets-binding element. Taken together, these results suggest that diverse interactions between Sp1/Sp3 and Ets factors are crucial for the SRG3 gene expression. |
doi_str_mv | 10.1016/j.bbrc.2005.10.107 |
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Drosophila SL2 cells, we found that various Sp or Ets family members activate the SRG3 promoter through these Sp- or Ets-binding sites, respectively, in a dose-dependent manner. Intriguingly, different combinatorial expression of Ets and Sp factors in SL2 cells resulted in either strong synergistic activation or repression of the SRG3 promoter activity. Moreover, the Sp-mediated activation of SRG3 promoter required the intact Ets-binding element. Taken together, these results suggest that diverse interactions between Sp1/Sp3 and Ets factors are crucial for the SRG3 gene expression.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2005.10.107</identifier><identifier>PMID: 16288722</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Base Sequence ; Binding Sites ; Cell Line ; Chromatin - chemistry ; Chromatin - metabolism ; Chromatin Assembly and Disassembly ; Drosophila ; Ets transcription factors ; Gene regulation ; Mice ; Mice, Inbred C57BL ; Promoter activity ; Promoter Regions, Genetic - genetics ; Protein Binding ; Proto-Oncogene Protein c-ets-1 - genetics ; Proto-Oncogene Protein c-ets-1 - metabolism ; Sp transcription factors ; Sp1 Transcription Factor - genetics ; Sp1 Transcription Factor - metabolism ; Sp3 Transcription Factor - genetics ; Sp3 Transcription Factor - metabolism ; SRG3 ; SWI/SNF chromatin-remodeling complex ; Transcription Factors - genetics ; Transcription Factors - metabolism</subject><ispartof>Biochemical and biophysical research communications, 2005-12, Vol.338 (3), p.1435-1446</ispartof><rights>2005 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c385t-69f76af17fc43be5508b307288c0a04c33c24af062228b95da0b7149c6b0dc6d3</citedby><cites>FETCH-LOGICAL-c385t-69f76af17fc43be5508b307288c0a04c33c24af062228b95da0b7149c6b0dc6d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0006291X05023594$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16288722$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ahn, Jeongeun</creatorcontrib><creatorcontrib>Ko, Myunggon</creatorcontrib><creatorcontrib>Lee, Kyuyoung</creatorcontrib><creatorcontrib>Oh, Jaehak</creatorcontrib><creatorcontrib>Jeon, Sung H.</creatorcontrib><creatorcontrib>Seong, Rho H.</creatorcontrib><title>Expression of SRG3, a core component of mouse SWI/SNF chromatin-remodeling complex, is regulated by cooperative interactions between Sp1/Sp3 and Ets transcription factors</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>SRG3, a mouse homolog of yeast SWI3 and human BAF155, is known to be a core component of SWI/SNF chromatin-remodeling complex. We have previously shown that SRG3 plays essential roles in early mouse embryogenesis, brain development, and T-cell development. SRG3 gene expression was differentially regulated depending on the developmental stages and exhibited tissue-specific pattern. In this study, we showed that the functional interactions between Sp and Ets family transcription factors are crucial for the SRG3 expression. Sp1 and Sp3 specifically bound to the two canonical Sp-binding sites (GC boxes) at −152 and −114, and a non-canonical Sp-binding site (CCTCCT motif) at −108 in the SRG3 promoter. Using
Drosophila SL2 cells, we found that various Sp or Ets family members activate the SRG3 promoter through these Sp- or Ets-binding sites, respectively, in a dose-dependent manner. Intriguingly, different combinatorial expression of Ets and Sp factors in SL2 cells resulted in either strong synergistic activation or repression of the SRG3 promoter activity. Moreover, the Sp-mediated activation of SRG3 promoter required the intact Ets-binding element. Taken together, these results suggest that diverse interactions between Sp1/Sp3 and Ets factors are crucial for the SRG3 gene expression.</description><subject>Animals</subject><subject>Base Sequence</subject><subject>Binding Sites</subject><subject>Cell Line</subject><subject>Chromatin - chemistry</subject><subject>Chromatin - metabolism</subject><subject>Chromatin Assembly and Disassembly</subject><subject>Drosophila</subject><subject>Ets transcription factors</subject><subject>Gene regulation</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Promoter activity</subject><subject>Promoter Regions, Genetic - genetics</subject><subject>Protein Binding</subject><subject>Proto-Oncogene Protein c-ets-1 - genetics</subject><subject>Proto-Oncogene Protein c-ets-1 - metabolism</subject><subject>Sp transcription factors</subject><subject>Sp1 Transcription Factor - genetics</subject><subject>Sp1 Transcription Factor - metabolism</subject><subject>Sp3 Transcription Factor - genetics</subject><subject>Sp3 Transcription Factor - metabolism</subject><subject>SRG3</subject><subject>SWI/SNF chromatin-remodeling complex</subject><subject>Transcription Factors - genetics</subject><subject>Transcription Factors - metabolism</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFu1DAQhi0EokvhBTggnzg1u2MncRKJC6q2pVJVJAKCW2Q7k-JVYgfbW9pX4ilxuiv1BpfxaOabf-T5CXnLYM2Aic1urZTXaw5Qrh9r1TOyYtBAxhkUz8kKAETGG_bjhLwKYQfAWCGal-SECV7XFecr8md7P3sMwThL3UDbL5f5GZVUO48pTLOzaOPSmdw-IG2_X23amwuqf3o3yWhs5nFyPY7G3j7yI96fUROox9v9KCP2VD2khpvRJ_wOqbExpTqmhYEqjL8RLW1ntmnnnErb020MNHppg_ZmXjA6JNz58Jq8GOQY8M3xPSXfLrZfzz9l158vr84_Xmc6r8uYiWaohBxYNegiV1iWUKscqvRhDRIKneeaF3IAwTmvVVP2ElTFikYLBb0WfX5K3h90Z-9-7THEbjJB4zhKi-kInahrqEVV_xdkTVPWDeMJ5AdQexeCx6GbvZmkf-gYdIuV3a5brOwWKw-1Kg29O6rv1YT908jRuwR8OACYjnFn0HdBG7Qae-NRx6535l_6fwGAJLHF</recordid><startdate>20051223</startdate><enddate>20051223</enddate><creator>Ahn, Jeongeun</creator><creator>Ko, Myunggon</creator><creator>Lee, Kyuyoung</creator><creator>Oh, Jaehak</creator><creator>Jeon, Sung H.</creator><creator>Seong, Rho H.</creator><general>Elsevier Inc</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>7TM</scope><scope>7X8</scope></search><sort><creationdate>20051223</creationdate><title>Expression of SRG3, a core component of mouse SWI/SNF chromatin-remodeling complex, is regulated by cooperative interactions between Sp1/Sp3 and Ets transcription factors</title><author>Ahn, Jeongeun ; Ko, Myunggon ; Lee, Kyuyoung ; Oh, Jaehak ; Jeon, Sung H. ; Seong, Rho H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c385t-69f76af17fc43be5508b307288c0a04c33c24af062228b95da0b7149c6b0dc6d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Base Sequence</topic><topic>Binding Sites</topic><topic>Cell Line</topic><topic>Chromatin - chemistry</topic><topic>Chromatin - metabolism</topic><topic>Chromatin Assembly and Disassembly</topic><topic>Drosophila</topic><topic>Ets transcription factors</topic><topic>Gene regulation</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Promoter activity</topic><topic>Promoter Regions, Genetic - genetics</topic><topic>Protein Binding</topic><topic>Proto-Oncogene Protein c-ets-1 - genetics</topic><topic>Proto-Oncogene Protein c-ets-1 - metabolism</topic><topic>Sp transcription factors</topic><topic>Sp1 Transcription Factor - genetics</topic><topic>Sp1 Transcription Factor - metabolism</topic><topic>Sp3 Transcription Factor - genetics</topic><topic>Sp3 Transcription Factor - metabolism</topic><topic>SRG3</topic><topic>SWI/SNF chromatin-remodeling complex</topic><topic>Transcription Factors - genetics</topic><topic>Transcription Factors - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ahn, Jeongeun</creatorcontrib><creatorcontrib>Ko, Myunggon</creatorcontrib><creatorcontrib>Lee, Kyuyoung</creatorcontrib><creatorcontrib>Oh, Jaehak</creatorcontrib><creatorcontrib>Jeon, Sung H.</creatorcontrib><creatorcontrib>Seong, Rho H.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ahn, Jeongeun</au><au>Ko, Myunggon</au><au>Lee, Kyuyoung</au><au>Oh, Jaehak</au><au>Jeon, Sung H.</au><au>Seong, Rho H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of SRG3, a core component of mouse SWI/SNF chromatin-remodeling complex, is regulated by cooperative interactions between Sp1/Sp3 and Ets transcription factors</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2005-12-23</date><risdate>2005</risdate><volume>338</volume><issue>3</issue><spage>1435</spage><epage>1446</epage><pages>1435-1446</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>SRG3, a mouse homolog of yeast SWI3 and human BAF155, is known to be a core component of SWI/SNF chromatin-remodeling complex. We have previously shown that SRG3 plays essential roles in early mouse embryogenesis, brain development, and T-cell development. SRG3 gene expression was differentially regulated depending on the developmental stages and exhibited tissue-specific pattern. In this study, we showed that the functional interactions between Sp and Ets family transcription factors are crucial for the SRG3 expression. Sp1 and Sp3 specifically bound to the two canonical Sp-binding sites (GC boxes) at −152 and −114, and a non-canonical Sp-binding site (CCTCCT motif) at −108 in the SRG3 promoter. Using
Drosophila SL2 cells, we found that various Sp or Ets family members activate the SRG3 promoter through these Sp- or Ets-binding sites, respectively, in a dose-dependent manner. Intriguingly, different combinatorial expression of Ets and Sp factors in SL2 cells resulted in either strong synergistic activation or repression of the SRG3 promoter activity. Moreover, the Sp-mediated activation of SRG3 promoter required the intact Ets-binding element. Taken together, these results suggest that diverse interactions between Sp1/Sp3 and Ets factors are crucial for the SRG3 gene expression.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>16288722</pmid><doi>10.1016/j.bbrc.2005.10.107</doi><tpages>12</tpages></addata></record> |
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subjects | Animals Base Sequence Binding Sites Cell Line Chromatin - chemistry Chromatin - metabolism Chromatin Assembly and Disassembly Drosophila Ets transcription factors Gene regulation Mice Mice, Inbred C57BL Promoter activity Promoter Regions, Genetic - genetics Protein Binding Proto-Oncogene Protein c-ets-1 - genetics Proto-Oncogene Protein c-ets-1 - metabolism Sp transcription factors Sp1 Transcription Factor - genetics Sp1 Transcription Factor - metabolism Sp3 Transcription Factor - genetics Sp3 Transcription Factor - metabolism SRG3 SWI/SNF chromatin-remodeling complex Transcription Factors - genetics Transcription Factors - metabolism |
title | Expression of SRG3, a core component of mouse SWI/SNF chromatin-remodeling complex, is regulated by cooperative interactions between Sp1/Sp3 and Ets transcription factors |
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