Pax6 controls the expression of critical genes involved in pancreatic {alpha} cell differentiation and function
The paired box homeodomain Pax6 is crucial for endocrine cell development and function and plays an essential role in glucose homeostasis. Indeed, mutations of Pax6 are associated with diabetic phenotype. Importantly, homozygous mutant mice for Pax6 are characterized by markedly decreased β and δ ce...
Gespeichert in:
Veröffentlicht in: | The Journal of biological chemistry 2010-10, Vol.285 (43), p.33381-33393 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 33393 |
---|---|
container_issue | 43 |
container_start_page | 33381 |
container_title | The Journal of biological chemistry |
container_volume | 285 |
creator | Gosmain, Yvan Marthinet, Eric Cheyssac, Claire Guérardel, Audrey Mamin, Aline Katz, Liora S Bouzakri, Karim Philippe, Jacques |
description | The paired box homeodomain Pax6 is crucial for endocrine cell development and function and plays an essential role in glucose homeostasis. Indeed, mutations of Pax6 are associated with diabetic phenotype. Importantly, homozygous mutant mice for Pax6 are characterized by markedly decreased β and δ cells and absent α cells. To better understand the critical role that Pax6 exerts in glucagon-producing cells, we developed a model of primary rat α cells. To study the transcriptional network of Pax6 in adult and differentiated α cells, we generated Pax6-deficient primary rat α cells and glucagon-producing cells, using either specific siRNA or cells expressing constitutively a dominant-negative form of Pax6. In primary rat α cells, we confirm that Pax6 controls the transcription of the Proglucagon and processing enzyme PC2 genes and identify three new target genes coding for MafB, cMaf, and NeuroD1/Beta2, which are all critical for Glucagon gene transcription and α cell differentiation. Furthermore, we demonstrate that Pax6 directly binds and activates the promoter region of the three genes through specific binding sites and that constitutive expression of a dominant-negative form of Pax6 in glucagon-producing cells (InR1G9) inhibits the activities of the promoters. Finally our results suggest that the critical role of Pax6 action on α cell differentiation is independent of those of Arx and Foxa2, two transcription factors that are necessary for α cell development. We conclude that Pax6 is critical for α cell function and differentiation through the transcriptional control of key genes involved in glucagon gene transcription, proglucagon processing, and α cell differentiation. |
doi_str_mv | 10.1074/jbc.M110.147215 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_856760721</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>759130483</sourcerecordid><originalsourceid>FETCH-LOGICAL-p873-d8276e3342f7834b804a7982c7d67552c8a5785fbd43b7a73e214965c9e475253</originalsourceid><addsrcrecordid>eNqFkL1PwzAQxS0EoqUwsyFvTCn-jJ0RVXxJRTB0YKsc50JdpXawk6oI8b-TijJzy93T--np9BC6pGRKiRI369JOn-leCcWoPEJjSjTPuKRvx2hMCKNZwaQeobOU1mQYUdBTNGJEFowwPkbh1exybIPvYmgS7laAYddGSMkFj0ONbXSds6bB7-AhYee3odlCNRy4Nd5GMIONv0zTrsw3ttA0uHJ1DRF85wZvSDG-wnXv7V6co5PaNAkuDnuCFvd3i9ljNn95eJrdzrNWK55VmqkcOBesVpqLUhNhVKGZVVWupGRWG6m0rMtK8FIZxYFRUeTSFiCUZJJP0PVvbBvDRw-pW25c2j9nPIQ-LbXMVU6Gyv4llSwoJ0Lzgbw6kH25gWrZRrcx8XP5Vyb_AVeldwo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>759130483</pqid></control><display><type>article</type><title>Pax6 controls the expression of critical genes involved in pancreatic {alpha} cell differentiation and function</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Gosmain, Yvan ; Marthinet, Eric ; Cheyssac, Claire ; Guérardel, Audrey ; Mamin, Aline ; Katz, Liora S ; Bouzakri, Karim ; Philippe, Jacques</creator><creatorcontrib>Gosmain, Yvan ; Marthinet, Eric ; Cheyssac, Claire ; Guérardel, Audrey ; Mamin, Aline ; Katz, Liora S ; Bouzakri, Karim ; Philippe, Jacques</creatorcontrib><description>The paired box homeodomain Pax6 is crucial for endocrine cell development and function and plays an essential role in glucose homeostasis. Indeed, mutations of Pax6 are associated with diabetic phenotype. Importantly, homozygous mutant mice for Pax6 are characterized by markedly decreased β and δ cells and absent α cells. To better understand the critical role that Pax6 exerts in glucagon-producing cells, we developed a model of primary rat α cells. To study the transcriptional network of Pax6 in adult and differentiated α cells, we generated Pax6-deficient primary rat α cells and glucagon-producing cells, using either specific siRNA or cells expressing constitutively a dominant-negative form of Pax6. In primary rat α cells, we confirm that Pax6 controls the transcription of the Proglucagon and processing enzyme PC2 genes and identify three new target genes coding for MafB, cMaf, and NeuroD1/Beta2, which are all critical for Glucagon gene transcription and α cell differentiation. Furthermore, we demonstrate that Pax6 directly binds and activates the promoter region of the three genes through specific binding sites and that constitutive expression of a dominant-negative form of Pax6 in glucagon-producing cells (InR1G9) inhibits the activities of the promoters. Finally our results suggest that the critical role of Pax6 action on α cell differentiation is independent of those of Arx and Foxa2, two transcription factors that are necessary for α cell development. We conclude that Pax6 is critical for α cell function and differentiation through the transcriptional control of key genes involved in glucagon gene transcription, proglucagon processing, and α cell differentiation.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M110.147215</identifier><identifier>PMID: 20592023</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Cell Differentiation - physiology ; Cell Line ; Eye Proteins - genetics ; Eye Proteins - metabolism ; Gene Expression Regulation - physiology ; Glucagon-Secreting Cells - cytology ; Glucagon-Secreting Cells - metabolism ; Homeodomain Proteins - genetics ; Homeodomain Proteins - metabolism ; Humans ; Mice ; Models, Biological ; Paired Box Transcription Factors - genetics ; Paired Box Transcription Factors - metabolism ; PAX6 Transcription Factor ; Proglucagon - biosynthesis ; Proglucagon - genetics ; Rats ; Repressor Proteins - genetics ; Repressor Proteins - metabolism ; Response Elements - physiology</subject><ispartof>The Journal of biological chemistry, 2010-10, Vol.285 (43), p.33381-33393</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20592023$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gosmain, Yvan</creatorcontrib><creatorcontrib>Marthinet, Eric</creatorcontrib><creatorcontrib>Cheyssac, Claire</creatorcontrib><creatorcontrib>Guérardel, Audrey</creatorcontrib><creatorcontrib>Mamin, Aline</creatorcontrib><creatorcontrib>Katz, Liora S</creatorcontrib><creatorcontrib>Bouzakri, Karim</creatorcontrib><creatorcontrib>Philippe, Jacques</creatorcontrib><title>Pax6 controls the expression of critical genes involved in pancreatic {alpha} cell differentiation and function</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>The paired box homeodomain Pax6 is crucial for endocrine cell development and function and plays an essential role in glucose homeostasis. Indeed, mutations of Pax6 are associated with diabetic phenotype. Importantly, homozygous mutant mice for Pax6 are characterized by markedly decreased β and δ cells and absent α cells. To better understand the critical role that Pax6 exerts in glucagon-producing cells, we developed a model of primary rat α cells. To study the transcriptional network of Pax6 in adult and differentiated α cells, we generated Pax6-deficient primary rat α cells and glucagon-producing cells, using either specific siRNA or cells expressing constitutively a dominant-negative form of Pax6. In primary rat α cells, we confirm that Pax6 controls the transcription of the Proglucagon and processing enzyme PC2 genes and identify three new target genes coding for MafB, cMaf, and NeuroD1/Beta2, which are all critical for Glucagon gene transcription and α cell differentiation. Furthermore, we demonstrate that Pax6 directly binds and activates the promoter region of the three genes through specific binding sites and that constitutive expression of a dominant-negative form of Pax6 in glucagon-producing cells (InR1G9) inhibits the activities of the promoters. Finally our results suggest that the critical role of Pax6 action on α cell differentiation is independent of those of Arx and Foxa2, two transcription factors that are necessary for α cell development. We conclude that Pax6 is critical for α cell function and differentiation through the transcriptional control of key genes involved in glucagon gene transcription, proglucagon processing, and α cell differentiation.</description><subject>Animals</subject><subject>Cell Differentiation - physiology</subject><subject>Cell Line</subject><subject>Eye Proteins - genetics</subject><subject>Eye Proteins - metabolism</subject><subject>Gene Expression Regulation - physiology</subject><subject>Glucagon-Secreting Cells - cytology</subject><subject>Glucagon-Secreting Cells - metabolism</subject><subject>Homeodomain Proteins - genetics</subject><subject>Homeodomain Proteins - metabolism</subject><subject>Humans</subject><subject>Mice</subject><subject>Models, Biological</subject><subject>Paired Box Transcription Factors - genetics</subject><subject>Paired Box Transcription Factors - metabolism</subject><subject>PAX6 Transcription Factor</subject><subject>Proglucagon - biosynthesis</subject><subject>Proglucagon - genetics</subject><subject>Rats</subject><subject>Repressor Proteins - genetics</subject><subject>Repressor Proteins - metabolism</subject><subject>Response Elements - physiology</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkL1PwzAQxS0EoqUwsyFvTCn-jJ0RVXxJRTB0YKsc50JdpXawk6oI8b-TijJzy93T--np9BC6pGRKiRI369JOn-leCcWoPEJjSjTPuKRvx2hMCKNZwaQeobOU1mQYUdBTNGJEFowwPkbh1exybIPvYmgS7laAYddGSMkFj0ONbXSds6bB7-AhYee3odlCNRy4Nd5GMIONv0zTrsw3ttA0uHJ1DRF85wZvSDG-wnXv7V6co5PaNAkuDnuCFvd3i9ljNn95eJrdzrNWK55VmqkcOBesVpqLUhNhVKGZVVWupGRWG6m0rMtK8FIZxYFRUeTSFiCUZJJP0PVvbBvDRw-pW25c2j9nPIQ-LbXMVU6Gyv4llSwoJ0Lzgbw6kH25gWrZRrcx8XP5Vyb_AVeldwo</recordid><startdate>20101022</startdate><enddate>20101022</enddate><creator>Gosmain, Yvan</creator><creator>Marthinet, Eric</creator><creator>Cheyssac, Claire</creator><creator>Guérardel, Audrey</creator><creator>Mamin, Aline</creator><creator>Katz, Liora S</creator><creator>Bouzakri, Karim</creator><creator>Philippe, Jacques</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20101022</creationdate><title>Pax6 controls the expression of critical genes involved in pancreatic {alpha} cell differentiation and function</title><author>Gosmain, Yvan ; Marthinet, Eric ; Cheyssac, Claire ; Guérardel, Audrey ; Mamin, Aline ; Katz, Liora S ; Bouzakri, Karim ; Philippe, Jacques</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p873-d8276e3342f7834b804a7982c7d67552c8a5785fbd43b7a73e214965c9e475253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Cell Differentiation - physiology</topic><topic>Cell Line</topic><topic>Eye Proteins - genetics</topic><topic>Eye Proteins - metabolism</topic><topic>Gene Expression Regulation - physiology</topic><topic>Glucagon-Secreting Cells - cytology</topic><topic>Glucagon-Secreting Cells - metabolism</topic><topic>Homeodomain Proteins - genetics</topic><topic>Homeodomain Proteins - metabolism</topic><topic>Humans</topic><topic>Mice</topic><topic>Models, Biological</topic><topic>Paired Box Transcription Factors - genetics</topic><topic>Paired Box Transcription Factors - metabolism</topic><topic>PAX6 Transcription Factor</topic><topic>Proglucagon - biosynthesis</topic><topic>Proglucagon - genetics</topic><topic>Rats</topic><topic>Repressor Proteins - genetics</topic><topic>Repressor Proteins - metabolism</topic><topic>Response Elements - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gosmain, Yvan</creatorcontrib><creatorcontrib>Marthinet, Eric</creatorcontrib><creatorcontrib>Cheyssac, Claire</creatorcontrib><creatorcontrib>Guérardel, Audrey</creatorcontrib><creatorcontrib>Mamin, Aline</creatorcontrib><creatorcontrib>Katz, Liora S</creatorcontrib><creatorcontrib>Bouzakri, Karim</creatorcontrib><creatorcontrib>Philippe, Jacques</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>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gosmain, Yvan</au><au>Marthinet, Eric</au><au>Cheyssac, Claire</au><au>Guérardel, Audrey</au><au>Mamin, Aline</au><au>Katz, Liora S</au><au>Bouzakri, Karim</au><au>Philippe, Jacques</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pax6 controls the expression of critical genes involved in pancreatic {alpha} cell differentiation and function</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2010-10-22</date><risdate>2010</risdate><volume>285</volume><issue>43</issue><spage>33381</spage><epage>33393</epage><pages>33381-33393</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>The paired box homeodomain Pax6 is crucial for endocrine cell development and function and plays an essential role in glucose homeostasis. Indeed, mutations of Pax6 are associated with diabetic phenotype. Importantly, homozygous mutant mice for Pax6 are characterized by markedly decreased β and δ cells and absent α cells. To better understand the critical role that Pax6 exerts in glucagon-producing cells, we developed a model of primary rat α cells. To study the transcriptional network of Pax6 in adult and differentiated α cells, we generated Pax6-deficient primary rat α cells and glucagon-producing cells, using either specific siRNA or cells expressing constitutively a dominant-negative form of Pax6. In primary rat α cells, we confirm that Pax6 controls the transcription of the Proglucagon and processing enzyme PC2 genes and identify three new target genes coding for MafB, cMaf, and NeuroD1/Beta2, which are all critical for Glucagon gene transcription and α cell differentiation. Furthermore, we demonstrate that Pax6 directly binds and activates the promoter region of the three genes through specific binding sites and that constitutive expression of a dominant-negative form of Pax6 in glucagon-producing cells (InR1G9) inhibits the activities of the promoters. Finally our results suggest that the critical role of Pax6 action on α cell differentiation is independent of those of Arx and Foxa2, two transcription factors that are necessary for α cell development. We conclude that Pax6 is critical for α cell function and differentiation through the transcriptional control of key genes involved in glucagon gene transcription, proglucagon processing, and α cell differentiation.</abstract><cop>United States</cop><pmid>20592023</pmid><doi>10.1074/jbc.M110.147215</doi><tpages>13</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9258 |
ispartof | The Journal of biological chemistry, 2010-10, Vol.285 (43), p.33381-33393 |
issn | 0021-9258 1083-351X |
language | eng |
recordid | cdi_proquest_miscellaneous_856760721 |
source | MEDLINE; EZB-FREE-00999 freely available EZB journals; PubMed Central; Alma/SFX Local Collection |
subjects | Animals Cell Differentiation - physiology Cell Line Eye Proteins - genetics Eye Proteins - metabolism Gene Expression Regulation - physiology Glucagon-Secreting Cells - cytology Glucagon-Secreting Cells - metabolism Homeodomain Proteins - genetics Homeodomain Proteins - metabolism Humans Mice Models, Biological Paired Box Transcription Factors - genetics Paired Box Transcription Factors - metabolism PAX6 Transcription Factor Proglucagon - biosynthesis Proglucagon - genetics Rats Repressor Proteins - genetics Repressor Proteins - metabolism Response Elements - physiology |
title | Pax6 controls the expression of critical genes involved in pancreatic {alpha} cell differentiation and function |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T11%3A48%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pax6%20controls%20the%20expression%20of%20critical%20genes%20involved%20in%20pancreatic%20%7Balpha%7D%20cell%20differentiation%20and%20function&rft.jtitle=The%20Journal%20of%20biological%20chemistry&rft.au=Gosmain,%20Yvan&rft.date=2010-10-22&rft.volume=285&rft.issue=43&rft.spage=33381&rft.epage=33393&rft.pages=33381-33393&rft.issn=0021-9258&rft.eissn=1083-351X&rft_id=info:doi/10.1074/jbc.M110.147215&rft_dat=%3Cproquest_pubme%3E759130483%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=759130483&rft_id=info:pmid/20592023&rfr_iscdi=true |