The zinc finger/homeodomain protein deltaEF1 mediates estrogen-specific induction of the ovalbumin gene
Regulation of the ovalbumin (Ov) gene is strictly controlled by precise developmental, tissue-specific, and hormonal cues. The Ov gene is transcriptionally activated by four classes of steroid hormones: estrogens, androgens, glucocorticoids, and progestins. Although it has served as a model to study...
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Veröffentlicht in: | Molecular and cellular endocrinology 2002-06, Vol.192 (1-2), p.85 |
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description | Regulation of the ovalbumin (Ov) gene is strictly controlled by precise developmental, tissue-specific, and hormonal cues. The Ov gene is transcriptionally activated by four classes of steroid hormones: estrogens, androgens, glucocorticoids, and progestins. Although it has served as a model to study multi-hormone gene regulation for the past 30 years, the pathways that relay each hormone signal to the Ov gene are largely unclear. Extensive linker-scanner and point mutation analysis has revealed elements necessary for its induction by estrogen, androgen, progesterone, or glucocorticoid but has failed to identify any elements that are specific to the action of any one steroid hormone. These observations in conjunction with the observation that the Ov gene is indirectly regulated by steroid hormones suggest that these signals may all induce the same transcription factor. However, here we have identified two cis-acting DNA elements in the 5' flanking region of the Ov gene that are required for induction by estrogen, but not by androgen or progesterone. These elements span -152 to -146 and -810 to -806 with respect to the start point of transcription. This implies that estrogen induces the Ov gene by a separate pathway than do androgens or progestins. Gel mobility shift assays demonstrate that the estrogen-specific sequences bind the estrogen inducible transcription factor deltaEF1, suggesting that deltaEF1 plays a distinct role in mediating the estrogen signal to the Ov gene. |
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The Ov gene is transcriptionally activated by four classes of steroid hormones: estrogens, androgens, glucocorticoids, and progestins. Although it has served as a model to study multi-hormone gene regulation for the past 30 years, the pathways that relay each hormone signal to the Ov gene are largely unclear. Extensive linker-scanner and point mutation analysis has revealed elements necessary for its induction by estrogen, androgen, progesterone, or glucocorticoid but has failed to identify any elements that are specific to the action of any one steroid hormone. These observations in conjunction with the observation that the Ov gene is indirectly regulated by steroid hormones suggest that these signals may all induce the same transcription factor. However, here we have identified two cis-acting DNA elements in the 5' flanking region of the Ov gene that are required for induction by estrogen, but not by androgen or progesterone. These elements span -152 to -146 and -810 to -806 with respect to the start point of transcription. This implies that estrogen induces the Ov gene by a separate pathway than do androgens or progestins. Gel mobility shift assays demonstrate that the estrogen-specific sequences bind the estrogen inducible transcription factor deltaEF1, suggesting that deltaEF1 plays a distinct role in mediating the estrogen signal to the Ov gene.</description><identifier>ISSN: 0303-7207</identifier><identifier>PMID: 12088870</identifier><language>eng</language><publisher>Ireland</publisher><subject>5' Flanking Region - genetics ; Animals ; Binding Sites ; Cells, Cultured - drug effects ; Cells, Cultured - metabolism ; Chickens ; Corticosterone - pharmacology ; Diethylstilbestrol - pharmacology ; Dihydrotestosterone - pharmacology ; Drug Implants ; Electrophoretic Mobility Shift Assay ; Estrogens - physiology ; Female ; Gene Expression Regulation - drug effects ; Homeodomain Proteins - physiology ; Mutation ; Ovalbumin - biosynthesis ; Ovalbumin - genetics ; Peptide Fragments - genetics ; Point Mutation ; Progesterone - pharmacology ; RNA, Messenger - biosynthesis ; Signal Transduction ; Transcription Factors - physiology ; Transcription, Genetic - drug effects ; Transfection ; Zinc Fingers - physiology</subject><ispartof>Molecular and cellular endocrinology, 2002-06, Vol.192 (1-2), p.85</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12088870$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dillner, Naomi B</creatorcontrib><creatorcontrib>Sanders, Michel M</creatorcontrib><title>The zinc finger/homeodomain protein deltaEF1 mediates estrogen-specific induction of the ovalbumin gene</title><title>Molecular and cellular endocrinology</title><addtitle>Mol Cell Endocrinol</addtitle><description>Regulation of the ovalbumin (Ov) gene is strictly controlled by precise developmental, tissue-specific, and hormonal cues. The Ov gene is transcriptionally activated by four classes of steroid hormones: estrogens, androgens, glucocorticoids, and progestins. Although it has served as a model to study multi-hormone gene regulation for the past 30 years, the pathways that relay each hormone signal to the Ov gene are largely unclear. Extensive linker-scanner and point mutation analysis has revealed elements necessary for its induction by estrogen, androgen, progesterone, or glucocorticoid but has failed to identify any elements that are specific to the action of any one steroid hormone. These observations in conjunction with the observation that the Ov gene is indirectly regulated by steroid hormones suggest that these signals may all induce the same transcription factor. However, here we have identified two cis-acting DNA elements in the 5' flanking region of the Ov gene that are required for induction by estrogen, but not by androgen or progesterone. These elements span -152 to -146 and -810 to -806 with respect to the start point of transcription. This implies that estrogen induces the Ov gene by a separate pathway than do androgens or progestins. Gel mobility shift assays demonstrate that the estrogen-specific sequences bind the estrogen inducible transcription factor deltaEF1, suggesting that deltaEF1 plays a distinct role in mediating the estrogen signal to the Ov gene.</description><subject>5' Flanking Region - genetics</subject><subject>Animals</subject><subject>Binding Sites</subject><subject>Cells, Cultured - drug effects</subject><subject>Cells, Cultured - metabolism</subject><subject>Chickens</subject><subject>Corticosterone - pharmacology</subject><subject>Diethylstilbestrol - pharmacology</subject><subject>Dihydrotestosterone - pharmacology</subject><subject>Drug Implants</subject><subject>Electrophoretic Mobility Shift Assay</subject><subject>Estrogens - physiology</subject><subject>Female</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Homeodomain Proteins - physiology</subject><subject>Mutation</subject><subject>Ovalbumin - biosynthesis</subject><subject>Ovalbumin - genetics</subject><subject>Peptide Fragments - genetics</subject><subject>Point Mutation</subject><subject>Progesterone - pharmacology</subject><subject>RNA, Messenger - biosynthesis</subject><subject>Signal Transduction</subject><subject>Transcription Factors - physiology</subject><subject>Transcription, Genetic - drug effects</subject><subject>Transfection</subject><subject>Zinc Fingers - physiology</subject><issn>0303-7207</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1j89KxDAYxHNQ3HX1FSQvUPzaNJvkKMuuCgse3PuSP1-6kTYpTSro01tQT8PAzI-ZK7IGBqwSDYgVuc35AwAEb-QNWdUNSCkFrEl3uiD9DtFSH2KH0-MlDZhcGnSIdJxSwUUd9kXvDzUd0AVdMFPMZUodxiqPaIMPloboZltCijR5WhZo-tS9mYelvuTwjlx73We8_9MNeT_sT7uX6vj2_Lp7OlYjb6HiqmWt2jqJDNq6NlYZhQqkVaLxrRDSKcuZNhydAuNwMdh4ZbjYIijFNuThlzrOZtl6Hqcw6Onr_P-X_QBVh1IX</recordid><startdate>20020628</startdate><enddate>20020628</enddate><creator>Dillner, Naomi B</creator><creator>Sanders, Michel M</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20020628</creationdate><title>The zinc finger/homeodomain protein deltaEF1 mediates estrogen-specific induction of the ovalbumin gene</title><author>Dillner, Naomi B ; Sanders, Michel M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p540-5943496d8e30411bc9b9e908c972f4778d9c53ab5ed90bdec53e2f9b576e0993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>5' Flanking Region - genetics</topic><topic>Animals</topic><topic>Binding Sites</topic><topic>Cells, Cultured - drug effects</topic><topic>Cells, Cultured - metabolism</topic><topic>Chickens</topic><topic>Corticosterone - pharmacology</topic><topic>Diethylstilbestrol - pharmacology</topic><topic>Dihydrotestosterone - pharmacology</topic><topic>Drug Implants</topic><topic>Electrophoretic Mobility Shift Assay</topic><topic>Estrogens - physiology</topic><topic>Female</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Homeodomain Proteins - physiology</topic><topic>Mutation</topic><topic>Ovalbumin - biosynthesis</topic><topic>Ovalbumin - genetics</topic><topic>Peptide Fragments - genetics</topic><topic>Point Mutation</topic><topic>Progesterone - pharmacology</topic><topic>RNA, Messenger - biosynthesis</topic><topic>Signal Transduction</topic><topic>Transcription Factors - physiology</topic><topic>Transcription, Genetic - drug effects</topic><topic>Transfection</topic><topic>Zinc Fingers - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dillner, Naomi B</creatorcontrib><creatorcontrib>Sanders, Michel M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Molecular and cellular endocrinology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dillner, Naomi B</au><au>Sanders, Michel M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The zinc finger/homeodomain protein deltaEF1 mediates estrogen-specific induction of the ovalbumin gene</atitle><jtitle>Molecular and cellular endocrinology</jtitle><addtitle>Mol Cell Endocrinol</addtitle><date>2002-06-28</date><risdate>2002</risdate><volume>192</volume><issue>1-2</issue><spage>85</spage><pages>85-</pages><issn>0303-7207</issn><abstract>Regulation of the ovalbumin (Ov) gene is strictly controlled by precise developmental, tissue-specific, and hormonal cues. The Ov gene is transcriptionally activated by four classes of steroid hormones: estrogens, androgens, glucocorticoids, and progestins. Although it has served as a model to study multi-hormone gene regulation for the past 30 years, the pathways that relay each hormone signal to the Ov gene are largely unclear. Extensive linker-scanner and point mutation analysis has revealed elements necessary for its induction by estrogen, androgen, progesterone, or glucocorticoid but has failed to identify any elements that are specific to the action of any one steroid hormone. These observations in conjunction with the observation that the Ov gene is indirectly regulated by steroid hormones suggest that these signals may all induce the same transcription factor. However, here we have identified two cis-acting DNA elements in the 5' flanking region of the Ov gene that are required for induction by estrogen, but not by androgen or progesterone. These elements span -152 to -146 and -810 to -806 with respect to the start point of transcription. This implies that estrogen induces the Ov gene by a separate pathway than do androgens or progestins. Gel mobility shift assays demonstrate that the estrogen-specific sequences bind the estrogen inducible transcription factor deltaEF1, suggesting that deltaEF1 plays a distinct role in mediating the estrogen signal to the Ov gene.</abstract><cop>Ireland</cop><pmid>12088870</pmid></addata></record> |
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source | MEDLINE; Elsevier ScienceDirect Journals Complete |
subjects | 5' Flanking Region - genetics Animals Binding Sites Cells, Cultured - drug effects Cells, Cultured - metabolism Chickens Corticosterone - pharmacology Diethylstilbestrol - pharmacology Dihydrotestosterone - pharmacology Drug Implants Electrophoretic Mobility Shift Assay Estrogens - physiology Female Gene Expression Regulation - drug effects Homeodomain Proteins - physiology Mutation Ovalbumin - biosynthesis Ovalbumin - genetics Peptide Fragments - genetics Point Mutation Progesterone - pharmacology RNA, Messenger - biosynthesis Signal Transduction Transcription Factors - physiology Transcription, Genetic - drug effects Transfection Zinc Fingers - physiology |
title | The zinc finger/homeodomain protein deltaEF1 mediates estrogen-specific induction of the ovalbumin gene |
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