The Zinc Finger Ikaros Transcription Factor Regulates Pituitary Growth Hormone and Prolactin Gene Expression through Distinct Effects on Chromatin Accessibility
The Ikaros transcription factors perform critical functions in the control of lymphohematopoiesis and immune regulation. Family members contain multiple zinc fingers that mediate DNA binding but have also been implicated as part of a complex chromatin-remodeling network. We show here that Ikaros is...
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Veröffentlicht in: | Molecular endocrinology (Baltimore, Md.) Md.), 2005-04, Vol.19 (4), p.1004-1011 |
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description | The Ikaros transcription factors perform critical functions in the control of lymphohematopoiesis and immune regulation. Family members contain multiple zinc fingers that mediate DNA binding but have also been implicated as part of a complex chromatin-remodeling network. We show here that Ikaros is expressed in pituitary mammosomatotrophs where it regulates the GH and prolactin (PRL) genes. Ikaros was detected by Northern and Western blotting in GH4 pituitary mammosomatotroph cells. Wild-type Ikaros (Ik1) inhibits GH mRNA and protein expression but stimulates PRL mRNA and protein levels. Ikaros does not bind directly to the proximal GH promoter but abrogates the effect of the histone deacetylation inhibitor trichostatin A on this region. Ikaros selectively deacetylates histone 3 residues on the proximal transfected or endogenous GH promoter and limits access of the Pit1 activator. In contrast, Ikaros acetylates histone 3 on the proximal PRL promoter and facilitates Pit1 binding to this region in the same cells. These data provide evidence for Ikaros-mediated histone acetylation and chromatin remodeling in the selective regulation of pituitary GH and PRL hormone gene expression. |
doi_str_mv | 10.1210/me.2004-0432 |
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Family members contain multiple zinc fingers that mediate DNA binding but have also been implicated as part of a complex chromatin-remodeling network. We show here that Ikaros is expressed in pituitary mammosomatotrophs where it regulates the GH and prolactin (PRL) genes. Ikaros was detected by Northern and Western blotting in GH4 pituitary mammosomatotroph cells. Wild-type Ikaros (Ik1) inhibits GH mRNA and protein expression but stimulates PRL mRNA and protein levels. Ikaros does not bind directly to the proximal GH promoter but abrogates the effect of the histone deacetylation inhibitor trichostatin A on this region. Ikaros selectively deacetylates histone 3 residues on the proximal transfected or endogenous GH promoter and limits access of the Pit1 activator. In contrast, Ikaros acetylates histone 3 on the proximal PRL promoter and facilitates Pit1 binding to this region in the same cells. These data provide evidence for Ikaros-mediated histone acetylation and chromatin remodeling in the selective regulation of pituitary GH and PRL hormone gene expression.</description><identifier>ISSN: 0888-8809</identifier><identifier>EISSN: 1944-9917</identifier><identifier>DOI: 10.1210/me.2004-0432</identifier><identifier>PMID: 15618287</identifier><language>eng</language><publisher>United States: Endocrine Society</publisher><subject>Acetylation - drug effects ; Animals ; Cells, Cultured ; Chromatin - metabolism ; DNA-Binding Proteins - genetics ; DNA-Binding Proteins - metabolism ; DNA-Binding Proteins - physiology ; Female ; Gene Expression Regulation ; Growth Hormone - genetics ; Growth Hormone - metabolism ; Histone Deacetylase Inhibitors ; Histones - metabolism ; Hydroxamic Acids - pharmacology ; Ikaros Transcription Factor ; Mice ; Pituitary Gland - cytology ; Pituitary Gland - metabolism ; Prolactin - genetics ; Prolactin - metabolism ; Promoter Regions, Genetic ; Rats ; RNA, Messenger - analysis ; RNA, Messenger - metabolism ; Transcription Factor Pit-1 ; Transcription Factors - genetics ; Transcription Factors - metabolism ; Transcription Factors - physiology ; Zinc Fingers</subject><ispartof>Molecular endocrinology (Baltimore, Md.), 2005-04, Vol.19 (4), p.1004-1011</ispartof><rights>Copyright © 2005 by The Endocrine Society 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-93d7a4daa8bfa1fadc04d1c088e37a2000dfad0e9d7102ab85eea93acb87c4293</citedby><cites>FETCH-LOGICAL-c396t-93d7a4daa8bfa1fadc04d1c088e37a2000dfad0e9d7102ab85eea93acb87c4293</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/15618287$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ezzat, Shereen</creatorcontrib><creatorcontrib>Yu, Shunjiang</creatorcontrib><creatorcontrib>Asa, Sylvia L</creatorcontrib><title>The Zinc Finger Ikaros Transcription Factor Regulates Pituitary Growth Hormone and Prolactin Gene Expression through Distinct Effects on Chromatin Accessibility</title><title>Molecular endocrinology (Baltimore, Md.)</title><addtitle>Mol Endocrinol</addtitle><description>The Ikaros transcription factors perform critical functions in the control of lymphohematopoiesis and immune regulation. Family members contain multiple zinc fingers that mediate DNA binding but have also been implicated as part of a complex chromatin-remodeling network. We show here that Ikaros is expressed in pituitary mammosomatotrophs where it regulates the GH and prolactin (PRL) genes. Ikaros was detected by Northern and Western blotting in GH4 pituitary mammosomatotroph cells. Wild-type Ikaros (Ik1) inhibits GH mRNA and protein expression but stimulates PRL mRNA and protein levels. Ikaros does not bind directly to the proximal GH promoter but abrogates the effect of the histone deacetylation inhibitor trichostatin A on this region. Ikaros selectively deacetylates histone 3 residues on the proximal transfected or endogenous GH promoter and limits access of the Pit1 activator. In contrast, Ikaros acetylates histone 3 on the proximal PRL promoter and facilitates Pit1 binding to this region in the same cells. These data provide evidence for Ikaros-mediated histone acetylation and chromatin remodeling in the selective regulation of pituitary GH and PRL hormone gene expression.</description><subject>Acetylation - drug effects</subject><subject>Animals</subject><subject>Cells, Cultured</subject><subject>Chromatin - metabolism</subject><subject>DNA-Binding Proteins - genetics</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>DNA-Binding Proteins - physiology</subject><subject>Female</subject><subject>Gene Expression Regulation</subject><subject>Growth Hormone - genetics</subject><subject>Growth Hormone - metabolism</subject><subject>Histone Deacetylase Inhibitors</subject><subject>Histones - metabolism</subject><subject>Hydroxamic Acids - pharmacology</subject><subject>Ikaros Transcription Factor</subject><subject>Mice</subject><subject>Pituitary Gland - cytology</subject><subject>Pituitary Gland - metabolism</subject><subject>Prolactin - genetics</subject><subject>Prolactin - metabolism</subject><subject>Promoter Regions, Genetic</subject><subject>Rats</subject><subject>RNA, Messenger - analysis</subject><subject>RNA, Messenger - metabolism</subject><subject>Transcription Factor Pit-1</subject><subject>Transcription Factors - genetics</subject><subject>Transcription Factors - metabolism</subject><subject>Transcription Factors - physiology</subject><subject>Zinc Fingers</subject><issn>0888-8809</issn><issn>1944-9917</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi0EotvCjTPyCS5NsfOxsY_VdndbqRIVWi5cook92XVJ7GA7gv4bfioOuxIXECdLM8-8st6HkDecXfGcsw8DXuWMlRkri_wZWXBZlpmUvH5OFkwIkQnB5Bk5D-GRMV5Wgr8kZ7xacpGLekF-7g5Ivxir6MbYPXp69xW8C3TnwQblzRiNs3QDKjpPP-F-6iFioA8mTiaCf6Jb777HA711fnAWKVhNH7zr04GxdItptP4xegxhzokH76b9gd6YkNYq0nXXoYqBpt0q7QaYr66VmvnW9CY-vSIvOugDvj69F-TzZr1b3Wb3H7d3q-v7TBVyGTNZ6BpKDSDaDngHWrFSc5UawKKGVBDTachQ6pqzHFpRIYIsQLWiVmUuiwvy7pg7evdtwhCbwQSFfQ8W3RSaZV0VQkjxX5AnkC_zKoGXR1ClQoPHrhm9GVJnDWfNrK4ZsJnVNbO6hL895U7tgPoPfHKVgPdHwE3jv6KyU1RxJNFqlyRa_G2geXSTt6nEv3_gFw7JtbA</recordid><startdate>200504</startdate><enddate>200504</enddate><creator>Ezzat, Shereen</creator><creator>Yu, Shunjiang</creator><creator>Asa, Sylvia L</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>7TK</scope><scope>7TM</scope><scope>7X8</scope></search><sort><creationdate>200504</creationdate><title>The Zinc Finger Ikaros Transcription Factor Regulates Pituitary Growth Hormone and Prolactin Gene Expression through Distinct Effects on Chromatin Accessibility</title><author>Ezzat, Shereen ; Yu, Shunjiang ; Asa, Sylvia L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-93d7a4daa8bfa1fadc04d1c088e37a2000dfad0e9d7102ab85eea93acb87c4293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Acetylation - drug effects</topic><topic>Animals</topic><topic>Cells, Cultured</topic><topic>Chromatin - metabolism</topic><topic>DNA-Binding Proteins - genetics</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>DNA-Binding Proteins - physiology</topic><topic>Female</topic><topic>Gene Expression Regulation</topic><topic>Growth Hormone - genetics</topic><topic>Growth Hormone - metabolism</topic><topic>Histone Deacetylase Inhibitors</topic><topic>Histones - metabolism</topic><topic>Hydroxamic Acids - pharmacology</topic><topic>Ikaros Transcription Factor</topic><topic>Mice</topic><topic>Pituitary Gland - cytology</topic><topic>Pituitary Gland - metabolism</topic><topic>Prolactin - genetics</topic><topic>Prolactin - metabolism</topic><topic>Promoter Regions, Genetic</topic><topic>Rats</topic><topic>RNA, Messenger - analysis</topic><topic>RNA, Messenger - metabolism</topic><topic>Transcription Factor Pit-1</topic><topic>Transcription Factors - genetics</topic><topic>Transcription Factors - metabolism</topic><topic>Transcription Factors - physiology</topic><topic>Zinc Fingers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ezzat, Shereen</creatorcontrib><creatorcontrib>Yu, Shunjiang</creatorcontrib><creatorcontrib>Asa, Sylvia L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular endocrinology (Baltimore, Md.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ezzat, Shereen</au><au>Yu, Shunjiang</au><au>Asa, Sylvia L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Zinc Finger Ikaros Transcription Factor Regulates Pituitary Growth Hormone and Prolactin Gene Expression through Distinct Effects on Chromatin Accessibility</atitle><jtitle>Molecular endocrinology (Baltimore, Md.)</jtitle><addtitle>Mol Endocrinol</addtitle><date>2005-04</date><risdate>2005</risdate><volume>19</volume><issue>4</issue><spage>1004</spage><epage>1011</epage><pages>1004-1011</pages><issn>0888-8809</issn><eissn>1944-9917</eissn><abstract>The Ikaros transcription factors perform critical functions in the control of lymphohematopoiesis and immune regulation. Family members contain multiple zinc fingers that mediate DNA binding but have also been implicated as part of a complex chromatin-remodeling network. We show here that Ikaros is expressed in pituitary mammosomatotrophs where it regulates the GH and prolactin (PRL) genes. Ikaros was detected by Northern and Western blotting in GH4 pituitary mammosomatotroph cells. Wild-type Ikaros (Ik1) inhibits GH mRNA and protein expression but stimulates PRL mRNA and protein levels. Ikaros does not bind directly to the proximal GH promoter but abrogates the effect of the histone deacetylation inhibitor trichostatin A on this region. Ikaros selectively deacetylates histone 3 residues on the proximal transfected or endogenous GH promoter and limits access of the Pit1 activator. In contrast, Ikaros acetylates histone 3 on the proximal PRL promoter and facilitates Pit1 binding to this region in the same cells. These data provide evidence for Ikaros-mediated histone acetylation and chromatin remodeling in the selective regulation of pituitary GH and PRL hormone gene expression.</abstract><cop>United States</cop><pub>Endocrine Society</pub><pmid>15618287</pmid><doi>10.1210/me.2004-0432</doi><tpages>8</tpages></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | Acetylation - drug effects Animals Cells, Cultured Chromatin - metabolism DNA-Binding Proteins - genetics DNA-Binding Proteins - metabolism DNA-Binding Proteins - physiology Female Gene Expression Regulation Growth Hormone - genetics Growth Hormone - metabolism Histone Deacetylase Inhibitors Histones - metabolism Hydroxamic Acids - pharmacology Ikaros Transcription Factor Mice Pituitary Gland - cytology Pituitary Gland - metabolism Prolactin - genetics Prolactin - metabolism Promoter Regions, Genetic Rats RNA, Messenger - analysis RNA, Messenger - metabolism Transcription Factor Pit-1 Transcription Factors - genetics Transcription Factors - metabolism Transcription Factors - physiology Zinc Fingers |
title | The Zinc Finger Ikaros Transcription Factor Regulates Pituitary Growth Hormone and Prolactin Gene Expression through Distinct Effects on Chromatin Accessibility |
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