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The Saccharomyces Cerevisiae RNA Polymerase III Recruitment Factor Subunits Brf1 and Bdp1 Impose a Strict Sequence Preference for the Downstream Half of the TATA Box

Overview
Specialty Biochemistry
Date 2006 Oct 10
PMID 17028095
Citations 2
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Abstract

Association of the TATA-binding protein (TBP) with its cognate site within eukaryotic promoters is key to accurate and efficient transcriptional initiation. To achieve recruitment of Saccharomyces cerevisiae RNA polymerase III, TBP is associated with two additional factors, Brf1 and Bdp1, to form the initiation factor TFIIIB. Previous data have suggested that the structure or dynamics of the TBP-DNA complex may be altered upon entry of Brf1 and Bdp1 into the complex. We show here, using the altered specificity TBP mutant TBPm3 and an iterative in vitro selection assay, that entry of Brf1 and Bdp1 into the complex imposes a strict sequence preference for the downstream half of the TATA box. Notably, the selected sequence (TGTAAATA) is a perfect match to the TATA box of the RNA polymerase III-transcribed U6 small nuclear RNA (SNR6) gene. We suggest that the selected T*A base pair step at the downstream end of the 8 bp TBP site may provide a DNA flexure that promotes TFIIIB-DNA complex formation.

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References
1.
Hoopes B, LeBlanc J, HAWLEY D . Kinetic analysis of yeast TFIID-TATA box complex formation suggests a multi-step pathway. J Biol Chem. 1992; 267(16):11539-47. View

2.
Strubin M, Struhl K . Yeast and human TFIID with altered DNA-binding specificity for TATA elements. Cell. 1992; 68(4):721-30. DOI: 10.1016/0092-8674(92)90147-5. View

3.
Kassavetis G, Joazeiro C, Pisano M, Geiduschek E, Colbert T, Hahn S . The role of the TATA-binding protein in the assembly and function of the multisubunit yeast RNA polymerase III transcription factor, TFIIIB. Cell. 1992; 71(6):1055-64. DOI: 10.1016/0092-8674(92)90399-w. View

4.
Kim Y, Geiger J, Hahn S, SIGLER P . Crystal structure of a yeast TBP/TATA-box complex. Nature. 1993; 365(6446):512-20. DOI: 10.1038/365512a0. View

5.
Kim J, Nikolov D, Burley S . Co-crystal structure of TBP recognizing the minor groove of a TATA element. Nature. 1993; 365(6446):520-7. DOI: 10.1038/365520a0. View