ARP1 interacts with the 5′ flanking region of the coagulation factor VII gene
Factor (F)VII plays a critical role in initiation of coagulation. Several segments within the 5′ flanking region of the FVII gene were previously demonstrated to recognize hepatic nuclear proteins, but few have been identified. To identify a regulatory protein binding the nuclear hormone response re...
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Veröffentlicht in: | Journal of thrombosis and haemostasis 2003-06, Vol.1 (6), p.1220-1227 |
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creator | Carew, J. A. Jackson, A. A. Bauer, K. A. |
description | Factor (F)VII plays a critical role in initiation of coagulation. Several segments within the 5′ flanking region of the FVII gene were previously demonstrated to recognize hepatic nuclear proteins, but few have been identified. To identify a regulatory protein binding the nuclear hormone response region (−237 to −200) of the FVII 5′ flanking region and demonstrate that the interaction is functional. Electrophoretic mobility shift assays and mutation analysis showed that ARP1, an orphan nuclear hormone receptor, interacted with two regions of the FVII 5′ flanking region, the hepatic nuclear factor 4 binding region (−77 to −47) and the nuclear hormone response region (−237 to −200). Transfection experiments demonstrated that reporter gene expression was decreased from vectors including the nuclear hormone response segment compared with that containing only the minimal promoter between positions −109 and +1, and that ARP1 also repressed expression through an interaction with the minimal promoter. These data indicate a role for ARP1 in transcriptional modulation of the FVII gene. |
doi_str_mv | 10.1046/j.1538-7836.2003.00227.x |
format | Article |
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A. ; Jackson, A. A. ; Bauer, K. A.</creator><creatorcontrib>Carew, J. A. ; Jackson, A. A. ; Bauer, K. A.</creatorcontrib><description>Factor (F)VII plays a critical role in initiation of coagulation. Several segments within the 5′ flanking region of the FVII gene were previously demonstrated to recognize hepatic nuclear proteins, but few have been identified. To identify a regulatory protein binding the nuclear hormone response region (−237 to −200) of the FVII 5′ flanking region and demonstrate that the interaction is functional. Electrophoretic mobility shift assays and mutation analysis showed that ARP1, an orphan nuclear hormone receptor, interacted with two regions of the FVII 5′ flanking region, the hepatic nuclear factor 4 binding region (−77 to −47) and the nuclear hormone response region (−237 to −200). Transfection experiments demonstrated that reporter gene expression was decreased from vectors including the nuclear hormone response segment compared with that containing only the minimal promoter between positions −109 and +1, and that ARP1 also repressed expression through an interaction with the minimal promoter. 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A.</creatorcontrib><creatorcontrib>Jackson, A. A.</creatorcontrib><creatorcontrib>Bauer, K. A.</creatorcontrib><title>ARP1 interacts with the 5′ flanking region of the coagulation factor VII gene</title><title>Journal of thrombosis and haemostasis</title><addtitle>J Thromb Haemost</addtitle><description>Factor (F)VII plays a critical role in initiation of coagulation. Several segments within the 5′ flanking region of the FVII gene were previously demonstrated to recognize hepatic nuclear proteins, but few have been identified. To identify a regulatory protein binding the nuclear hormone response region (−237 to −200) of the FVII 5′ flanking region and demonstrate that the interaction is functional. Electrophoretic mobility shift assays and mutation analysis showed that ARP1, an orphan nuclear hormone receptor, interacted with two regions of the FVII 5′ flanking region, the hepatic nuclear factor 4 binding region (−77 to −47) and the nuclear hormone response region (−237 to −200). Transfection experiments demonstrated that reporter gene expression was decreased from vectors including the nuclear hormone response segment compared with that containing only the minimal promoter between positions −109 and +1, and that ARP1 also repressed expression through an interaction with the minimal promoter. These data indicate a role for ARP1 in transcriptional modulation of the FVII gene.</description><subject>5' Flanking Region - genetics</subject><subject>Basic Helix-Loop-Helix Leucine Zipper Transcription Factors</subject><subject>Binding Sites</subject><subject>Cell Line, Tumor</subject><subject>coagulation</subject><subject>COUP Transcription Factor II</subject><subject>COUP Transcription Factors</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>DNA-Binding Proteins - physiology</subject><subject>factor VII</subject><subject>Factor VII - genetics</subject><subject>Genes, Reporter</subject><subject>Hepatocyte Nuclear Factor 4</subject><subject>Humans</subject><subject>Phosphoproteins - genetics</subject><subject>Promoter Regions, Genetic</subject><subject>Receptors, Glucocorticoid - genetics</subject><subject>Receptors, Steroid</subject><subject>Response Elements</subject><subject>transcription</subject><subject>Transcription Factors - genetics</subject><subject>Transcription Factors - metabolism</subject><subject>Transcription Factors - physiology</subject><subject>Transcription, Genetic - genetics</subject><subject>Transfection</subject><issn>1538-7933</issn><issn>1538-7836</issn><issn>1538-7836</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkEtOwzAQhi0EouVxBeQVuwa_EicSm6oCWlSpCBW2luPaaUqaFDtR2x1n4kicBKctsGU1o5n_n8cHAMQowIhFN4sAhzTu8ZhGAUGIBggRwoPNEej-No5_8oTSDjhzboEQTkKCTkEHk5hjSmgXTPrPTxjmZa2tVLWD67yew3quYfj18QlNIcu3vMyg1VlelbAyu56qZNYUsm5LxtsqC19HI5jpUl-AEyMLpy8P8Ry83N9NB8PeePIwGvTHPUUjxnsyZMpwhU2UKkVSRVMsOY8SjGQaKv9RQpAmTBoehhRLhmZhgmc8Zcb_pA2m5-B6P3dlq_dGu1osc6d04Q_WVeMEp4xiFjEvjPdCZSvnrDZiZfOltFuBkWhhioVoOYmWmWhhih1MsfHWq8OOJl3q2Z_xQM8LbveCdV7o7b8Hi8fp0Cf0G-vOglk</recordid><startdate>200306</startdate><enddate>200306</enddate><creator>Carew, J. A.</creator><creator>Jackson, A. A.</creator><creator>Bauer, K. A.</creator><general>Blackwell Science 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>7X8</scope></search><sort><creationdate>200306</creationdate><title>ARP1 interacts with the 5′ flanking region of the coagulation factor VII gene</title><author>Carew, J. A. ; Jackson, A. A. ; Bauer, K. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3647-a54cf7c1f6bcc2bc3b1a776910ab5c003920e24af75531a40d591d7b4f153ef13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>5' Flanking Region - genetics</topic><topic>Basic Helix-Loop-Helix Leucine Zipper Transcription Factors</topic><topic>Binding Sites</topic><topic>Cell Line, Tumor</topic><topic>coagulation</topic><topic>COUP Transcription Factor II</topic><topic>COUP Transcription Factors</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>DNA-Binding Proteins - physiology</topic><topic>factor VII</topic><topic>Factor VII - genetics</topic><topic>Genes, Reporter</topic><topic>Hepatocyte Nuclear Factor 4</topic><topic>Humans</topic><topic>Phosphoproteins - genetics</topic><topic>Promoter Regions, Genetic</topic><topic>Receptors, Glucocorticoid - genetics</topic><topic>Receptors, Steroid</topic><topic>Response Elements</topic><topic>transcription</topic><topic>Transcription Factors - genetics</topic><topic>Transcription Factors - metabolism</topic><topic>Transcription Factors - physiology</topic><topic>Transcription, Genetic - genetics</topic><topic>Transfection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Carew, J. A.</creatorcontrib><creatorcontrib>Jackson, A. A.</creatorcontrib><creatorcontrib>Bauer, K. A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of thrombosis and haemostasis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Carew, J. A.</au><au>Jackson, A. A.</au><au>Bauer, K. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ARP1 interacts with the 5′ flanking region of the coagulation factor VII gene</atitle><jtitle>Journal of thrombosis and haemostasis</jtitle><addtitle>J Thromb Haemost</addtitle><date>2003-06</date><risdate>2003</risdate><volume>1</volume><issue>6</issue><spage>1220</spage><epage>1227</epage><pages>1220-1227</pages><issn>1538-7933</issn><issn>1538-7836</issn><eissn>1538-7836</eissn><abstract>Factor (F)VII plays a critical role in initiation of coagulation. Several segments within the 5′ flanking region of the FVII gene were previously demonstrated to recognize hepatic nuclear proteins, but few have been identified. To identify a regulatory protein binding the nuclear hormone response region (−237 to −200) of the FVII 5′ flanking region and demonstrate that the interaction is functional. Electrophoretic mobility shift assays and mutation analysis showed that ARP1, an orphan nuclear hormone receptor, interacted with two regions of the FVII 5′ flanking region, the hepatic nuclear factor 4 binding region (−77 to −47) and the nuclear hormone response region (−237 to −200). Transfection experiments demonstrated that reporter gene expression was decreased from vectors including the nuclear hormone response segment compared with that containing only the minimal promoter between positions −109 and +1, and that ARP1 also repressed expression through an interaction with the minimal promoter. These data indicate a role for ARP1 in transcriptional modulation of the FVII gene.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Inc</pub><pmid>12871323</pmid><doi>10.1046/j.1538-7836.2003.00227.x</doi><tpages>8</tpages></addata></record> |
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subjects | 5' Flanking Region - genetics Basic Helix-Loop-Helix Leucine Zipper Transcription Factors Binding Sites Cell Line, Tumor coagulation COUP Transcription Factor II COUP Transcription Factors DNA-Binding Proteins - metabolism DNA-Binding Proteins - physiology factor VII Factor VII - genetics Genes, Reporter Hepatocyte Nuclear Factor 4 Humans Phosphoproteins - genetics Promoter Regions, Genetic Receptors, Glucocorticoid - genetics Receptors, Steroid Response Elements transcription Transcription Factors - genetics Transcription Factors - metabolism Transcription Factors - physiology Transcription, Genetic - genetics Transfection |
title | ARP1 interacts with the 5′ flanking region of the coagulation factor VII gene |
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