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PMID: 1586948 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Variants of the TATA-binding protein can distinguish subsets of RNA polymerase I, II, and III promoters.

Cell ·Vol. 69 ·No. 4 ·1992-05-15 ·Pages 697-702

Schultz MC, Reeder RH, Hahn S

Abstract

Transcription extracts prepared from yeast that are deficient in the TATA-binding protein (TBP or TFIID) are also impaired in specific promoter recognition by all three nuclear RNA polymerases (pol I, II, and III). Specific initiation can be rescued by the addition of purified recombinant TBP, demonstrating that pol I, II, and III all require this factor. A mutation of TBP has been identified that will function with pol I but not with pol II or III. Conversely, another mutation, which inactivates TATA element binding in vitro, will function with pol I and III promoters but is inactive for a pol II promoter. Thus, it is possible to identify TBP variants that will only function on different subsets of all nuclear promoters.

Related Genes
MeSH Terms
DNA-Binding Proteins/physiology Mutation Promoter Regions, Genetic RNA Polymerase I/metabolism RNA Polymerase II/metabolism RNA Polymerase III/metabolism Recombinant Proteins/metabolism Saccharomyces cerevisiae/genetics TATA-Box Binding Protein Temperature Transcription Factor TFIID Transcription Factors/physiology Transcription, Genetic
Chemicals
DNA-Binding Proteins Recombinant Proteins TATA-Box Binding Protein Transcription Factor TFIID Transcription Factors RNA Polymerase II RNA Polymerase I RNA Polymerase III
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Schultz M C
Hutchinson Cancer Research Center, Seattle, Washington 98104.
Reeder R H
Hahn S
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1992-05-15
Pages
697-702
Language
English
Region
United States
NLM ID
0413066
Subset
IM
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