Abstract
The three-dimensional structure of wild-type yeast RNA polymerase II has been determined at a nominal resolution of 24 A. A difference map between this structure and that of the polymerase lacking subunits Rpb4 and Rpb7 showed these two subunits forming part of the floor of the DNA-binding (active center) cleft, and revealed a slight inward movement of the protein domain surrounding the cleft. Surface plasmon resonance measurements showed that Rpb4 and Rpb7 stabilize a minimal pre-initiation complex containing promoter DNA, TATA box-binding protein (TBP), transcription factor TFIIB and the polymerase. These findings suggest that Rpb4 and Rpb7 play a role in coupling the entry of DNA into the active center cleft to closure of the cleft. Such a role can explain why these subunits are necessary for promoter-specific transcription in vitro and for a normal stress response in vivo.
MeSH Terms
Binding Sites
Crystallography, X-Ray
DNA/metabolism
DNA-Binding Proteins/metabolism
Models, Molecular
RNA Polymerase II/chemistry,genetics,metabolism
Saccharomyces cerevisiae/enzymology
Structure-Activity Relationship
TATA-Box Binding Protein
Transcription Factor TFIIB
Transcription Factors/metabolism
Chemicals
DNA-Binding Proteins
TATA-Box Binding Protein
Transcription Factor TFIIB
Transcription Factors
DNA
RNA Polymerase II
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Jensen G J
Department of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Meredith G
Bushnell D A
Kornberg R D
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