Pbx1 is a co-factor for Cdx-2 in regulating proglucagon gene expression in pancreatic A cells
A number of Hox and Hox-like homeodomain (HD) proteins have been previously shown to utilize members of the TALE HD protein family as co-factors in regulating gene expression. The caudal HD protein Cdx-2 is a transactivator for the proglucagon gene, expressed in pancreatic A cells and intestinal end...
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Veröffentlicht in: | Molecular and cellular endocrinology 2006-04, Vol.249 (1-2), p.140-149 |
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creator | Liu, Tao Branch, Donald R. Jin, Tianru |
description | A number of Hox and Hox-like homeodomain (HD) proteins have been previously shown to utilize members of the TALE HD protein family as co-factors in regulating gene expression. The caudal HD protein Cdx-2 is a transactivator for the proglucagon gene, expressed in pancreatic A cells and intestinal endocrine L cells. We demonstrate here that co-transfection of the TALE homeobox gene Pbx1 enhanced the activation of Cdx-2 on the proglucagon promoter in either the pancreatic A cell line InR1-G9 or BHK fibroblasts. The activation was observed for proglucagon promoter constructs with or without the binding motifs for Pbx1. Furthermore, mutating the penta-peptide motif (binding motif for TALE HD proteins) on Cdx-2 substantially attenuated its activation on proglucagon promoter, but not on the sucrase–isomaltase gene (SI) promoter, or its own (Cdx-2) promoter; suggesting that Cdx-2 utilizes Pbx1 as a co-factor for regulating the expression of selected target genes. Physical interaction between Cdx-2 and Pbx1 was demonstrated by co-immunoprecipitation as well as GST fusion protein pull-down. We suggest that this study reveals a novel function for Pbx1 in pancreatic islet physiology: regulating proglucagon expression by serving as a co-factor for Cdx-2. |
doi_str_mv | 10.1016/j.mce.2006.02.007 |
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The caudal HD protein Cdx-2 is a transactivator for the proglucagon gene, expressed in pancreatic A cells and intestinal endocrine L cells. We demonstrate here that co-transfection of the TALE homeobox gene Pbx1 enhanced the activation of Cdx-2 on the proglucagon promoter in either the pancreatic A cell line InR1-G9 or BHK fibroblasts. The activation was observed for proglucagon promoter constructs with or without the binding motifs for Pbx1. Furthermore, mutating the penta-peptide motif (binding motif for TALE HD proteins) on Cdx-2 substantially attenuated its activation on proglucagon promoter, but not on the sucrase–isomaltase gene (SI) promoter, or its own (Cdx-2) promoter; suggesting that Cdx-2 utilizes Pbx1 as a co-factor for regulating the expression of selected target genes. Physical interaction between Cdx-2 and Pbx1 was demonstrated by co-immunoprecipitation as well as GST fusion protein pull-down. We suggest that this study reveals a novel function for Pbx1 in pancreatic islet physiology: regulating proglucagon expression by serving as a co-factor for Cdx-2.</description><identifier>ISSN: 0303-7207</identifier><identifier>EISSN: 1872-8057</identifier><identifier>DOI: 10.1016/j.mce.2006.02.007</identifier><identifier>PMID: 16574312</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Amino Acid Motifs ; Animals ; Cdx-2 ; CDX2 Transcription Factor ; Cell Line ; Cricetinae ; DNA-Binding Proteins - chemistry ; DNA-Binding Proteins - metabolism ; DNA-Binding Proteins - physiology ; Gene Expression Regulation ; Glucagon-Secreting Cells - metabolism ; GST pull down ; Homeobox gene ; Homeodomain Proteins - chemistry ; Homeodomain Proteins - metabolism ; Humans ; Pbx1 ; Pre-B-Cell Leukemia Transcription Factor 1 ; Proglucagon ; Proglucagon - genetics ; Proglucagon - metabolism ; Promoter Regions, Genetic ; Protein Interaction Mapping ; Proto-Oncogene Proteins - chemistry ; Proto-Oncogene Proteins - metabolism ; Proto-Oncogene Proteins - physiology ; Trans-Activators - chemistry ; Trans-Activators - metabolism</subject><ispartof>Molecular and cellular endocrinology, 2006-04, Vol.249 (1-2), p.140-149</ispartof><rights>2006 Elsevier Ireland Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c382t-a6586f5e3e73fb25784ba40356824fb3673fcd78806676bdcd3a87c1f44e2e533</citedby><cites>FETCH-LOGICAL-c382t-a6586f5e3e73fb25784ba40356824fb3673fcd78806676bdcd3a87c1f44e2e533</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.mce.2006.02.007$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16574312$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Tao</creatorcontrib><creatorcontrib>Branch, Donald R.</creatorcontrib><creatorcontrib>Jin, Tianru</creatorcontrib><title>Pbx1 is a co-factor for Cdx-2 in regulating proglucagon gene expression in pancreatic A cells</title><title>Molecular and cellular endocrinology</title><addtitle>Mol Cell Endocrinol</addtitle><description>A number of Hox and Hox-like homeodomain (HD) proteins have been previously shown to utilize members of the TALE HD protein family as co-factors in regulating gene expression. The caudal HD protein Cdx-2 is a transactivator for the proglucagon gene, expressed in pancreatic A cells and intestinal endocrine L cells. We demonstrate here that co-transfection of the TALE homeobox gene Pbx1 enhanced the activation of Cdx-2 on the proglucagon promoter in either the pancreatic A cell line InR1-G9 or BHK fibroblasts. The activation was observed for proglucagon promoter constructs with or without the binding motifs for Pbx1. Furthermore, mutating the penta-peptide motif (binding motif for TALE HD proteins) on Cdx-2 substantially attenuated its activation on proglucagon promoter, but not on the sucrase–isomaltase gene (SI) promoter, or its own (Cdx-2) promoter; suggesting that Cdx-2 utilizes Pbx1 as a co-factor for regulating the expression of selected target genes. Physical interaction between Cdx-2 and Pbx1 was demonstrated by co-immunoprecipitation as well as GST fusion protein pull-down. We suggest that this study reveals a novel function for Pbx1 in pancreatic islet physiology: regulating proglucagon expression by serving as a co-factor for Cdx-2.</description><subject>Amino Acid Motifs</subject><subject>Animals</subject><subject>Cdx-2</subject><subject>CDX2 Transcription Factor</subject><subject>Cell Line</subject><subject>Cricetinae</subject><subject>DNA-Binding Proteins - chemistry</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>DNA-Binding Proteins - physiology</subject><subject>Gene Expression Regulation</subject><subject>Glucagon-Secreting Cells - metabolism</subject><subject>GST pull down</subject><subject>Homeobox gene</subject><subject>Homeodomain Proteins - chemistry</subject><subject>Homeodomain Proteins - metabolism</subject><subject>Humans</subject><subject>Pbx1</subject><subject>Pre-B-Cell Leukemia Transcription Factor 1</subject><subject>Proglucagon</subject><subject>Proglucagon - genetics</subject><subject>Proglucagon - metabolism</subject><subject>Promoter Regions, Genetic</subject><subject>Protein Interaction Mapping</subject><subject>Proto-Oncogene Proteins - chemistry</subject><subject>Proto-Oncogene Proteins - metabolism</subject><subject>Proto-Oncogene Proteins - physiology</subject><subject>Trans-Activators - chemistry</subject><subject>Trans-Activators - metabolism</subject><issn>0303-7207</issn><issn>1872-8057</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1r3DAQhkVJ6W62_QG9FJ1yszuSrI-lp7CkTSDQHJpjELI8Nlq89layw-bfR9td6C05DMMMz7wMDyFfGZQMmPq-LXceSw6gSuAlgP5AlsxoXhiQ-oIsQYAoNAe9IJcpbSETkptPZMGU1JVgfEmeHuoDoyFRR_1YtM5PY6Rtrk1zKDgNA43Yzb2bwtDRfRy7fvauGwfa4YAUD_uIKYU8Z3LvBh8xo55eU499nz6Tj63rE3459xV5_HnzZ3Nb3P_-dbe5vi-8MHwqnJJGtRIFatHWXGpT1a4CIZXhVVsLlde-0caAUlrVjW-EM9qztqqQoxRiRa5OufnDvzOmye5COn7gBhznZJU2goOR74JsvVaKgc4gO4E-jilFbO0-hp2LL5aBPcq3W5vl26N8C9zCv5tv5_C53mHz_-JsOwM_TgBmF88Bo00-4OCxCRH9ZJsxvBH_Cl7zk3M</recordid><startdate>20060425</startdate><enddate>20060425</enddate><creator>Liu, Tao</creator><creator>Branch, Donald R.</creator><creator>Jin, Tianru</creator><general>Elsevier Ireland Ltd</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>20060425</creationdate><title>Pbx1 is a co-factor for Cdx-2 in regulating proglucagon gene expression in pancreatic A cells</title><author>Liu, Tao ; Branch, Donald R. ; Jin, Tianru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c382t-a6586f5e3e73fb25784ba40356824fb3673fcd78806676bdcd3a87c1f44e2e533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Amino Acid Motifs</topic><topic>Animals</topic><topic>Cdx-2</topic><topic>CDX2 Transcription Factor</topic><topic>Cell Line</topic><topic>Cricetinae</topic><topic>DNA-Binding Proteins - chemistry</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>DNA-Binding Proteins - physiology</topic><topic>Gene Expression Regulation</topic><topic>Glucagon-Secreting Cells - metabolism</topic><topic>GST pull down</topic><topic>Homeobox gene</topic><topic>Homeodomain Proteins - chemistry</topic><topic>Homeodomain Proteins - metabolism</topic><topic>Humans</topic><topic>Pbx1</topic><topic>Pre-B-Cell Leukemia Transcription Factor 1</topic><topic>Proglucagon</topic><topic>Proglucagon - genetics</topic><topic>Proglucagon - metabolism</topic><topic>Promoter Regions, Genetic</topic><topic>Protein Interaction Mapping</topic><topic>Proto-Oncogene Proteins - chemistry</topic><topic>Proto-Oncogene Proteins - metabolism</topic><topic>Proto-Oncogene Proteins - physiology</topic><topic>Trans-Activators - chemistry</topic><topic>Trans-Activators - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Tao</creatorcontrib><creatorcontrib>Branch, Donald R.</creatorcontrib><creatorcontrib>Jin, Tianru</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>Molecular and cellular endocrinology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Tao</au><au>Branch, Donald R.</au><au>Jin, Tianru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pbx1 is a co-factor for Cdx-2 in regulating proglucagon gene expression in pancreatic A cells</atitle><jtitle>Molecular and cellular endocrinology</jtitle><addtitle>Mol Cell Endocrinol</addtitle><date>2006-04-25</date><risdate>2006</risdate><volume>249</volume><issue>1-2</issue><spage>140</spage><epage>149</epage><pages>140-149</pages><issn>0303-7207</issn><eissn>1872-8057</eissn><abstract>A number of Hox and Hox-like homeodomain (HD) proteins have been previously shown to utilize members of the TALE HD protein family as co-factors in regulating gene expression. The caudal HD protein Cdx-2 is a transactivator for the proglucagon gene, expressed in pancreatic A cells and intestinal endocrine L cells. We demonstrate here that co-transfection of the TALE homeobox gene Pbx1 enhanced the activation of Cdx-2 on the proglucagon promoter in either the pancreatic A cell line InR1-G9 or BHK fibroblasts. The activation was observed for proglucagon promoter constructs with or without the binding motifs for Pbx1. Furthermore, mutating the penta-peptide motif (binding motif for TALE HD proteins) on Cdx-2 substantially attenuated its activation on proglucagon promoter, but not on the sucrase–isomaltase gene (SI) promoter, or its own (Cdx-2) promoter; suggesting that Cdx-2 utilizes Pbx1 as a co-factor for regulating the expression of selected target genes. Physical interaction between Cdx-2 and Pbx1 was demonstrated by co-immunoprecipitation as well as GST fusion protein pull-down. We suggest that this study reveals a novel function for Pbx1 in pancreatic islet physiology: regulating proglucagon expression by serving as a co-factor for Cdx-2.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>16574312</pmid><doi>10.1016/j.mce.2006.02.007</doi><tpages>10</tpages></addata></record> |
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subjects | Amino Acid Motifs Animals Cdx-2 CDX2 Transcription Factor Cell Line Cricetinae DNA-Binding Proteins - chemistry DNA-Binding Proteins - metabolism DNA-Binding Proteins - physiology Gene Expression Regulation Glucagon-Secreting Cells - metabolism GST pull down Homeobox gene Homeodomain Proteins - chemistry Homeodomain Proteins - metabolism Humans Pbx1 Pre-B-Cell Leukemia Transcription Factor 1 Proglucagon Proglucagon - genetics Proglucagon - metabolism Promoter Regions, Genetic Protein Interaction Mapping Proto-Oncogene Proteins - chemistry Proto-Oncogene Proteins - metabolism Proto-Oncogene Proteins - physiology Trans-Activators - chemistry Trans-Activators - metabolism |
title | Pbx1 is a co-factor for Cdx-2 in regulating proglucagon gene expression in pancreatic A cells |
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