Tsihlis Nick D, Grove Anne
Department of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA.
Nucleic Acids Res. 2006;34(19):5585-93. doi: 10.1093/nar/gkl534. Epub 2006 Oct 6.
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.
TATA 结合蛋白(TBP)与真核生物启动子内其同源位点的结合是准确高效转录起始的关键。为了实现酿酒酵母RNA聚合酶III的募集,TBP与另外两个因子Brf1和Bdp1结合,形成起始因子TFIIIB。先前的数据表明,Brf1和Bdp1进入复合物后,TBP-DNA复合物的结构或动力学可能会发生改变。我们在此使用特异性改变的TBP突变体TBPm3和迭代体外选择试验表明,Brf1和Bdp1进入复合物对TATA框的下游半部分施加了严格的序列偏好。值得注意的是,所选序列(TGTAAATA)与RNA聚合酶III转录的U6小核RNA(SNR6)基因的TATA框完全匹配。我们认为,在8 bp TBP位点下游末端选择的T*A碱基对步移可能提供促进TFIIIB-DNA复合物形成的DNA弯曲。