FOXA3 Is Expressed in Multiple Cell Lineages in the Mouse Testis and Regulates Pdgfra Expression in Leydig Cells
The three FOXA transcription factors are mainly known for their roles in the liver. However, Foxa3-deficient mice become progressively sub/infertile due to germ cell loss. Because no data were available regarding the localization of the FOXA3 protein in the testis, immunohistochemistry was performed...
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Veröffentlicht in: | Endocrinology (Philadelphia) 2017-06, Vol.158 (6), p.1886-1897 |
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creator | Garon, Gabriel Bergeron, Francis Brousseau, Catherine Robert, Nicholas M. Tremblay, Jacques J. |
description | The three FOXA transcription factors are mainly known for their roles in the liver. However, Foxa3-deficient mice become progressively sub/infertile due to germ cell loss. Because no data were available regarding the localization of the FOXA3 protein in the testis, immunohistochemistry was performed on mouse testis sections. In the fetal testis, a weak but consistent staining for FOXA3 is detected in the nucleus of Sertoli cells. In prepubertal and adult life, FOXA3 remains present in Sertoli cells of some but not all seminiferous tubules. FOXA3 is also detected in the nucleus of some peritubular cells. From postnatal day 20 onward, FOXA3 is strongly expressed in the nucleus of Leydig cells. To identify FOXA3 target genes in Leydig cells, MLTC-1 Leydig cells were transfected with a series of Leydig cell gene reporters in the presence of a FOXA3 expression vector. The platelet-derived growth factor receptor α (Pdgfra) promoter was significantly activated by FOXA3. The Pdgfra promoter contains three potential FOX elements and progressive 5′ deletions and site-directed mutagenesis revealed that the most proximal element at −78 bp was sufficient to confer FOXA3 responsiveness. FOXA3 from Leydig cells could bind to this element in vitro (electrophoretic mobility shift assay) and was recruited to the proximal Pdgfra promoter in vivo (chromatin immunoprecipitation). Finally, endogenous Pdgfra messenger RNA levels were reduced in FOXA3-deficient MLTC-1 Leydig cells. Taken together, our data identify FOXA3 as a marker of the Sertoli cell lineage and of the adult Leydig cell population, and as a regulator of Pdgfra transcription in Leydig cells.The FOXA3 transcription factor is differentially expressed in Sertoli and peritubular cells, as well as in the adult population of Leydig cells, and contributes to Pdgfra transcription in Leydig cells. |
doi_str_mv | 10.1210/en.2016-1736 |
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However, Foxa3-deficient mice become progressively sub/infertile due to germ cell loss. Because no data were available regarding the localization of the FOXA3 protein in the testis, immunohistochemistry was performed on mouse testis sections. In the fetal testis, a weak but consistent staining for FOXA3 is detected in the nucleus of Sertoli cells. In prepubertal and adult life, FOXA3 remains present in Sertoli cells of some but not all seminiferous tubules. FOXA3 is also detected in the nucleus of some peritubular cells. From postnatal day 20 onward, FOXA3 is strongly expressed in the nucleus of Leydig cells. To identify FOXA3 target genes in Leydig cells, MLTC-1 Leydig cells were transfected with a series of Leydig cell gene reporters in the presence of a FOXA3 expression vector. The platelet-derived growth factor receptor α (Pdgfra) promoter was significantly activated by FOXA3. The Pdgfra promoter contains three potential FOX elements and progressive 5′ deletions and site-directed mutagenesis revealed that the most proximal element at −78 bp was sufficient to confer FOXA3 responsiveness. FOXA3 from Leydig cells could bind to this element in vitro (electrophoretic mobility shift assay) and was recruited to the proximal Pdgfra promoter in vivo (chromatin immunoprecipitation). Finally, endogenous Pdgfra messenger RNA levels were reduced in FOXA3-deficient MLTC-1 Leydig cells. Taken together, our data identify FOXA3 as a marker of the Sertoli cell lineage and of the adult Leydig cell population, and as a regulator of Pdgfra transcription in Leydig cells.The FOXA3 transcription factor is differentially expressed in Sertoli and peritubular cells, as well as in the adult population of Leydig cells, and contributes to Pdgfra transcription in Leydig cells.</description><identifier>ISSN: 0013-7227</identifier><identifier>EISSN: 1945-7170</identifier><identifier>DOI: 10.1210/en.2016-1736</identifier><identifier>PMID: 28379539</identifier><language>eng</language><publisher>Washington, DC: Endocrine Society</publisher><subject>Animals ; Cell Line ; Cell lineage ; Cell Lineage - genetics ; Chromatin ; Electrophoretic mobility ; Endocrinology ; Fetuses ; Foxa3 protein ; Gene expression ; Gene Expression Regulation ; Growth factors ; Hepatocyte Nuclear Factor 3-gamma - genetics ; Hepatocytes ; Immunohistochemistry ; Immunoprecipitation ; Leydig cells ; Leydig Cells - metabolism ; Liver ; Localization ; Male ; Mice ; mRNA ; Nuclei ; Nuclei (cytology) ; Platelet-derived growth factor ; Platelet-derived growth factor receptors ; Rats ; Receptor, Platelet-Derived Growth Factor alpha - genetics ; Receptor, Platelet-Derived Growth Factor alpha - metabolism ; Ribonucleic acid ; RNA ; Rodents ; Sertoli cells ; Site-directed mutagenesis ; Target recognition ; Testis - cytology ; Testis - metabolism ; Transcription factors ; Tubules</subject><ispartof>Endocrinology (Philadelphia), 2017-06, Vol.158 (6), p.1886-1897</ispartof><rights>Copyright © 2017 Endocrine Society 2017</rights><rights>Copyright © 2017 Endocrine Society.</rights><rights>Copyright © 2017 Endocrine Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c417t-663b4d8e4b766ddcf128a4f5bd04b20948012920d29566606d8ba6af3bcabb863</citedby><cites>FETCH-LOGICAL-c417t-663b4d8e4b766ddcf128a4f5bd04b20948012920d29566606d8ba6af3bcabb863</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28379539$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Garon, Gabriel</creatorcontrib><creatorcontrib>Bergeron, Francis</creatorcontrib><creatorcontrib>Brousseau, Catherine</creatorcontrib><creatorcontrib>Robert, Nicholas M.</creatorcontrib><creatorcontrib>Tremblay, Jacques J.</creatorcontrib><title>FOXA3 Is Expressed in Multiple Cell Lineages in the Mouse Testis and Regulates Pdgfra Expression in Leydig Cells</title><title>Endocrinology (Philadelphia)</title><addtitle>Endocrinology</addtitle><description>The three FOXA transcription factors are mainly known for their roles in the liver. However, Foxa3-deficient mice become progressively sub/infertile due to germ cell loss. Because no data were available regarding the localization of the FOXA3 protein in the testis, immunohistochemistry was performed on mouse testis sections. In the fetal testis, a weak but consistent staining for FOXA3 is detected in the nucleus of Sertoli cells. In prepubertal and adult life, FOXA3 remains present in Sertoli cells of some but not all seminiferous tubules. FOXA3 is also detected in the nucleus of some peritubular cells. From postnatal day 20 onward, FOXA3 is strongly expressed in the nucleus of Leydig cells. To identify FOXA3 target genes in Leydig cells, MLTC-1 Leydig cells were transfected with a series of Leydig cell gene reporters in the presence of a FOXA3 expression vector. The platelet-derived growth factor receptor α (Pdgfra) promoter was significantly activated by FOXA3. The Pdgfra promoter contains three potential FOX elements and progressive 5′ deletions and site-directed mutagenesis revealed that the most proximal element at −78 bp was sufficient to confer FOXA3 responsiveness. FOXA3 from Leydig cells could bind to this element in vitro (electrophoretic mobility shift assay) and was recruited to the proximal Pdgfra promoter in vivo (chromatin immunoprecipitation). Finally, endogenous Pdgfra messenger RNA levels were reduced in FOXA3-deficient MLTC-1 Leydig cells. Taken together, our data identify FOXA3 as a marker of the Sertoli cell lineage and of the adult Leydig cell population, and as a regulator of Pdgfra transcription in Leydig cells.The FOXA3 transcription factor is differentially expressed in Sertoli and peritubular cells, as well as in the adult population of Leydig cells, and contributes to Pdgfra transcription in Leydig cells.</description><subject>Animals</subject><subject>Cell Line</subject><subject>Cell lineage</subject><subject>Cell Lineage - genetics</subject><subject>Chromatin</subject><subject>Electrophoretic mobility</subject><subject>Endocrinology</subject><subject>Fetuses</subject><subject>Foxa3 protein</subject><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>Growth factors</subject><subject>Hepatocyte Nuclear Factor 3-gamma - genetics</subject><subject>Hepatocytes</subject><subject>Immunohistochemistry</subject><subject>Immunoprecipitation</subject><subject>Leydig cells</subject><subject>Leydig Cells - metabolism</subject><subject>Liver</subject><subject>Localization</subject><subject>Male</subject><subject>Mice</subject><subject>mRNA</subject><subject>Nuclei</subject><subject>Nuclei (cytology)</subject><subject>Platelet-derived growth factor</subject><subject>Platelet-derived growth factor receptors</subject><subject>Rats</subject><subject>Receptor, Platelet-Derived Growth Factor alpha - genetics</subject><subject>Receptor, Platelet-Derived Growth Factor alpha - metabolism</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Rodents</subject><subject>Sertoli cells</subject><subject>Site-directed mutagenesis</subject><subject>Target recognition</subject><subject>Testis - cytology</subject><subject>Testis - metabolism</subject><subject>Transcription factors</subject><subject>Tubules</subject><issn>0013-7227</issn><issn>1945-7170</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1r2zAYh8VYWdNut52HYIfuUHf6sj6OITRtIaVlZLCbkKzXmYtje5YNzX8_uUl7KLQnIfTo4QcPQl8puaCMkp_QXDBCZUYVlx_QjBqRZ4oq8hHNCKE8U4ypY3QS40O6CiH4J3TMNFcm52aGuuXdnznHNxFfPnY9xAgBVw2-Heuh6mrAC6hrvKoacBuI08vwF_BtO0bAa4hDFbFrAv4Fm7F2QyLuw6bs3bOsapvpzwp2odo8ueJndFS6OsKXw3mKfi8v14vrbHV3dbOYr7JCUDVkUnIvggbhlZQhFCVl2oky94EIz4gRmlBmGAnM5FJKIoP2TrqS-8J5ryU_RT_23q5v_41pqt1WsUgLXANpvqVaCyGFVCKh31-hD-3YN2md5ZQTRXMt2XsUNdIYwZlSiTrfU0XfxthDabu-2rp-ZymxUy8LjZ162alXwr8dpKPfQniBnwMl4GwPtGP3luopPf8PdWuZxQ</recordid><startdate>20170601</startdate><enddate>20170601</enddate><creator>Garon, Gabriel</creator><creator>Bergeron, Francis</creator><creator>Brousseau, Catherine</creator><creator>Robert, Nicholas M.</creator><creator>Tremblay, Jacques J.</creator><general>Endocrine Society</general><general>Oxford University Press</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>7QG</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20170601</creationdate><title>FOXA3 Is Expressed in Multiple Cell Lineages in the Mouse Testis and Regulates Pdgfra Expression in Leydig Cells</title><author>Garon, Gabriel ; Bergeron, Francis ; Brousseau, Catherine ; Robert, Nicholas M. ; Tremblay, Jacques J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-663b4d8e4b766ddcf128a4f5bd04b20948012920d29566606d8ba6af3bcabb863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Cell Line</topic><topic>Cell lineage</topic><topic>Cell Lineage - genetics</topic><topic>Chromatin</topic><topic>Electrophoretic mobility</topic><topic>Endocrinology</topic><topic>Fetuses</topic><topic>Foxa3 protein</topic><topic>Gene expression</topic><topic>Gene Expression Regulation</topic><topic>Growth factors</topic><topic>Hepatocyte Nuclear Factor 3-gamma - genetics</topic><topic>Hepatocytes</topic><topic>Immunohistochemistry</topic><topic>Immunoprecipitation</topic><topic>Leydig cells</topic><topic>Leydig Cells - metabolism</topic><topic>Liver</topic><topic>Localization</topic><topic>Male</topic><topic>Mice</topic><topic>mRNA</topic><topic>Nuclei</topic><topic>Nuclei (cytology)</topic><topic>Platelet-derived growth factor</topic><topic>Platelet-derived growth factor receptors</topic><topic>Rats</topic><topic>Receptor, Platelet-Derived Growth Factor alpha - genetics</topic><topic>Receptor, Platelet-Derived Growth Factor alpha - metabolism</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>Rodents</topic><topic>Sertoli cells</topic><topic>Site-directed mutagenesis</topic><topic>Target recognition</topic><topic>Testis - cytology</topic><topic>Testis - metabolism</topic><topic>Transcription factors</topic><topic>Tubules</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Garon, Gabriel</creatorcontrib><creatorcontrib>Bergeron, Francis</creatorcontrib><creatorcontrib>Brousseau, Catherine</creatorcontrib><creatorcontrib>Robert, Nicholas M.</creatorcontrib><creatorcontrib>Tremblay, Jacques J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Endocrinology (Philadelphia)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Garon, Gabriel</au><au>Bergeron, Francis</au><au>Brousseau, Catherine</au><au>Robert, Nicholas M.</au><au>Tremblay, Jacques J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>FOXA3 Is Expressed in Multiple Cell Lineages in the Mouse Testis and Regulates Pdgfra Expression in Leydig Cells</atitle><jtitle>Endocrinology (Philadelphia)</jtitle><addtitle>Endocrinology</addtitle><date>2017-06-01</date><risdate>2017</risdate><volume>158</volume><issue>6</issue><spage>1886</spage><epage>1897</epage><pages>1886-1897</pages><issn>0013-7227</issn><eissn>1945-7170</eissn><abstract>The three FOXA transcription factors are mainly known for their roles in the liver. However, Foxa3-deficient mice become progressively sub/infertile due to germ cell loss. Because no data were available regarding the localization of the FOXA3 protein in the testis, immunohistochemistry was performed on mouse testis sections. In the fetal testis, a weak but consistent staining for FOXA3 is detected in the nucleus of Sertoli cells. In prepubertal and adult life, FOXA3 remains present in Sertoli cells of some but not all seminiferous tubules. FOXA3 is also detected in the nucleus of some peritubular cells. From postnatal day 20 onward, FOXA3 is strongly expressed in the nucleus of Leydig cells. To identify FOXA3 target genes in Leydig cells, MLTC-1 Leydig cells were transfected with a series of Leydig cell gene reporters in the presence of a FOXA3 expression vector. The platelet-derived growth factor receptor α (Pdgfra) promoter was significantly activated by FOXA3. The Pdgfra promoter contains three potential FOX elements and progressive 5′ deletions and site-directed mutagenesis revealed that the most proximal element at −78 bp was sufficient to confer FOXA3 responsiveness. FOXA3 from Leydig cells could bind to this element in vitro (electrophoretic mobility shift assay) and was recruited to the proximal Pdgfra promoter in vivo (chromatin immunoprecipitation). Finally, endogenous Pdgfra messenger RNA levels were reduced in FOXA3-deficient MLTC-1 Leydig cells. Taken together, our data identify FOXA3 as a marker of the Sertoli cell lineage and of the adult Leydig cell population, and as a regulator of Pdgfra transcription in Leydig cells.The FOXA3 transcription factor is differentially expressed in Sertoli and peritubular cells, as well as in the adult population of Leydig cells, and contributes to Pdgfra transcription in Leydig cells.</abstract><cop>Washington, DC</cop><pub>Endocrine Society</pub><pmid>28379539</pmid><doi>10.1210/en.2016-1736</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cell Line Cell lineage Cell Lineage - genetics Chromatin Electrophoretic mobility Endocrinology Fetuses Foxa3 protein Gene expression Gene Expression Regulation Growth factors Hepatocyte Nuclear Factor 3-gamma - genetics Hepatocytes Immunohistochemistry Immunoprecipitation Leydig cells Leydig Cells - metabolism Liver Localization Male Mice mRNA Nuclei Nuclei (cytology) Platelet-derived growth factor Platelet-derived growth factor receptors Rats Receptor, Platelet-Derived Growth Factor alpha - genetics Receptor, Platelet-Derived Growth Factor alpha - metabolism Ribonucleic acid RNA Rodents Sertoli cells Site-directed mutagenesis Target recognition Testis - cytology Testis - metabolism Transcription factors Tubules |
title | FOXA3 Is Expressed in Multiple Cell Lineages in the Mouse Testis and Regulates Pdgfra Expression in Leydig Cells |
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