A Yeast TATA-Binding Protein Mutant That Selectively Enhances Gene Expression from Weak RNA Polymerase II Promoters
Author(s) -
Wade Blair,
Bryan R. Cullen
Publication year - 1997
Publication title -
molecular and cellular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.14
H-Index - 327
eISSN - 1067-8824
pISSN - 0270-7306
DOI - 10.1128/mcb.17.5.2888
Subject(s) - transcription factor ii d , biology , transcription factor ii a , tata box , promoter , taf1 , general transcription factor , tata binding protein , taf2 , rna polymerase ii , transcription (linguistics) , tata box binding protein , microbiology and biotechnology , taf4 , rna polymerase ii holoenzyme , genetics , gene expression , gene , linguistics , philosophy
We describe a unique gain-of-function mutant of the TATA-binding protein (TBP) subunit of Saccharomyces cerevisiae TFIID that, at least in part, renders transcriptional transactivators dispensable for efficient mRNA expression. The yTBPN69S mutant enhances transcription from weaker yeast promoter elements by up to 50-fold yet does not significantly increase gene expression directed by highly active promoters. Therefore, this TBP mutant and transcriptional transactivators appear to affect a common rate-limiting step in transcription initiation. Consistent with the hypothesis that this step is TFIID recruitment, tethering of TBP to a target promoter via a heterologous DNA binding domain, which is known to bypass the need for transcriptional transactivators, also nullifies the enhancing effect exerted by the N69S mutation. These data provide genetic support for the hypothesis that TFIID recruitment represents a rate-limiting step in the initiation of mRNA transcription that is specifically enhanced by transcriptional transactivators.
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