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PMID: 9150136 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Repression by Ume6 involves recruitment of a complex containing Sin3 corepressor and Rpd3 histone deacetylase to target promoters.

Cell ·Vol. 89 ·No. 3 ·1997-05-02 ·Pages 365-71

Kadosh D, Struhl K

Abstract

Sin3 and Rpd3 negatively regulate a diverse set of yeast genes. A mouse Sin3-related protein is a transcriptional corepressor, and a human Rpd3 homolog is a histone deacetylase. Here, we show that Sin3 and Rpd3 are specifically required for transcriptional repression by Ume6, a DNA-binding protein that regulates genes involved in meiosis. A short region of Ume6 is sufficient to repress transcription, and this repression domain mediates a two-hybrid and physical interaction with Sin3. Coimmunoprecipitation and two-hybrid experiments indicate that Sin3 and Rpd3 are associated in a complex distinct from TFIID and Pol II holoenzyme. Rpd3 is specifically required for repression by Sin3, and artificial recruitment of Rpd3 results in repression. These results suggest that repression by Ume6 involves recruitment of a Sin3-Rpd3 complex and targeted histone deacetylation.

MeSH Terms
DNA-Binding Proteins/chemistry,genetics,metabolism Fungal Proteins/chemistry,genetics,metabolism Gene Expression Regulation, Enzymologic/physiology Gene Expression Regulation, Fungal/physiology Histone Deacetylases/genetics,metabolism Multienzyme Complexes/physiology Promoter Regions, Genetic/physiology Protein Binding/physiology Protein Structure, Tertiary Repressor Proteins/genetics,metabolism Saccharomyces cerevisiae Proteins Transcription Factors/chemistry,genetics,metabolism Transcription, Genetic/physiology Yeasts/enzymology beta-Galactosidase/genetics,metabolism
Chemicals
DNA-Binding Proteins Fungal Proteins Multienzyme Complexes Repressor Proteins SIN3 protein, S cerevisiae Saccharomyces cerevisiae Proteins Transcription Factors UME6 protein, S cerevisiae beta-Galactosidase Histone Deacetylases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Kadosh D
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Struhl K
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1997-05-02
Pages
365-71
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NIGMS NIH HHS · GM 53720 · United States
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