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PMID: 2685558 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Functional distinctions between yeast TATA elements.

Molecular and cellular biology ·Vol. 9 ·No. 12 ·1989-12-00 ·Pages 5298-304

Harbury PA, Struhl K

Abstract

Although the yeast his3 promoter region contains two functional TATA elements, TR and TC, the GCN4 and GAL4 upstream activator proteins stimulate transcription only through TR. In combination with GAL4, an oligonucleotide containing the sequence TATAAA is fully sufficient for TR function, whereas almost all single-base-pair substitutions of this sequence abolish the ability of this element to activate transcription. Further analysis of these and other mutations of the TR element led to the following conclusions. First, sequences downstream of the TATAAA sequence are important for TR function. Second, a double mutant, TATTTA, can serve as a TR element even though the corresponding single mutation, TATTAA, is unable to do so. Third, three mutations have the novel property of being able to activate transcription in combination with GCN4 but not with GAL4; this finding suggests that activation by GCN4 and by GAL4 may not occur by identical mechanisms. From these observations, we address the question of whether there is a single TATA-binding factor required for the transcription of all genes.

MeSH Terms
Alleles Base Sequence Gene Expression Gene Expression Regulation, Fungal Genes, Fungal Molecular Sequence Data Mutation Promoter Regions, Genetic Restriction Mapping Saccharomyces cerevisiae/genetics Transcription, Genetic
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Harbury P A
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115.
Struhl K
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Article Info
Journal
Molecular and cellular biology
Abbr.
Mol Cell Biol
ISSN
0270-7306
Published
1989-12-00
Pages
5298-304
Language
English
Region
United States
NLM ID
8109087
PMCID
PMC363694
Subset
IM
Grants
NIGMS NIH HHS · GM 30186 · United States
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