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PMID: 3192076 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Hormone-mediated repression: a negative glucocorticoid response element from the bovine prolactin gene.

Genes & development ·Vol. 2 ·No. 9 ·1988-09-00 ·Pages 1144-54

Sakai DD, Helms S, Carlstedt-Duke J, Gustafsson JA, Rottman FM, Yamamoto KR

Abstract

We have defined and characterized a region upstream of the bovine prolactin gene that confers repression by glucocorticoids. This 'negative glucocorticoid response element' (nGRE) contains multiple footprinting sites for purified glucocorticoid receptor protein between -51 and -562 bp. A strong consensus sequence for receptor binding within the nGRE has not yet been defined, but it is apparent that nGRE sequences differ from the GRE consensus elements that confer positive glucocorticoid regulation. Unlike 'positive' GREs, the nGRE enhances promoter activity in the absence of glucocorticoids or receptor, presumably through the action of a protein that binds in the same region and activates transcription. The hormone-receptor complex appears to negate this enhancement by competing or inactivating the second factor. As with positive GREs, nGRE sequences confer hormonal regulation upon linked heterologous promoters within various cell types; a 34-bp subfragment containing a single receptor binding site is sufficient for nGRE activity. We speculate that nGRE sequences might alter the structure of bound receptor, thereby preventing it from functioning as a positive regulator when bound at those sites.

MeSH Terms
Animals Base Sequence Cattle Deoxyribonuclease I/analysis Gene Expression Regulation Genetic Linkage Glucocorticoids/genetics,physiology Molecular Sequence Data Nucleotide Mapping Prolactin/genetics Receptors, Glucocorticoid/metabolism Repressor Proteins/physiology Transcription Factors/physiology
Chemicals
Glucocorticoids Receptors, Glucocorticoid Repressor Proteins Transcription Factors Prolactin Deoxyribonuclease I
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Sakai D D
Department of Biochemistry and Biophysics, University of California, San Francisco 94143-0448.
Helms S
Carlstedt-Duke J
Gustafsson J A
Rottman F M
Yamamoto K R
Article Info
Journal
Genes & development
Abbr.
Genes Dev
ISSN
0890-9369
Published
1988-09-00
Pages
1144-54
Language
English
Region
United States
NLM ID
8711660
Subset
IM
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