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PMID: 9822614 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Association of distinct yeast Not2 functional domains with components of Gcn5 histone acetylase and Ccr4 transcriptional regulatory complexes.

The EMBO journal ·Vol. 17 ·No. 22 ·1998-11-16 ·Pages 6714-22

Benson JD, Benson M, Howley PM, Struhl K

Abstract

The NOT genes were originally identified in a yeast genetic screen that selected mutations resulting in increased utilization of a non-consensus TC TATA element of the HIS3 promoter. Here, we present evidence that the N-terminus of Not2 interacts with components of the Ada/Gcn5 histone acetyltransferase complex. Loss of this interaction either through abrogation of Not2 N-terminal function or deletion of ada2 or gcn5 results in derepression of the HIS3 TC element. This suggests that association of Not2 with the Ada/Gcn5 histone acetyltransferase complex is involved in regulation of the HIS3 promoter. Association between the Not and CCR4 transcriptional regulatory complexes has also been observed recently. Our phenotypic analyses suggest that these CCR4-related Not2 functions are mediated by a functionally independent domain of Not2 that includes the highly conserved C-terminus. Chimeric proteins containing the yeast Not2 N-terminus fused to the human C-terminus function in yeast, suggesting that the Not2 C-terminus represents a distinct modular domain whose function is conserved between higher and lower eukaryotes.

MeSH Terms
Acetyltransferases/metabolism Amino Acid Sequence Bacterial Proteins/genetics Cell Cycle Proteins/genetics,metabolism DNA-Binding Proteins Fungal Proteins/genetics,metabolism Histone Acetyltransferases Humans Hydro-Lyases/genetics Molecular Sequence Data Promoter Regions, Genetic Protein Binding Protein Kinases/metabolism Recombinant Fusion Proteins/genetics,metabolism Repressor Proteins/genetics,metabolism Ribonucleases Saccharomyces cerevisiae Proteins Serine Endopeptidases/genetics Transcription Factors/metabolism
Chemicals
Bacterial Proteins CDC36 protein, S cerevisiae Cell Cycle Proteins DNA-Binding Proteins Fungal Proteins LexA protein, Bacteria Recombinant Fusion Proteins Repressor Proteins Saccharomyces cerevisiae Proteins Transcription Factors Acetyltransferases GCN5 protein, S cerevisiae Histone Acetyltransferases Protein Kinases CCR4 protein, S cerevisiae Ribonucleases Serine Endopeptidases Hydro-Lyases imidazoleglycerolphosphate dehydratase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Benson J D
Department of Pathology, Harvard Medical School, Boston, MA 02115, USA.
Benson M
Howley P M
Struhl K
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43 references, click to expand
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Article Info
Journal
The EMBO journal
Abbr.
EMBO J
ISSN
0261-4189
Published
1998-11-16
Pages
6714-22
Language
English
Region
England
NLM ID
8208664
PMCID
PMC1171016
Subset
IM
Grants
NIGMS NIH HHS · GM30186 · United States
NIGMS NIH HHS · GM53720 · United States
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