Kays A R, Schepartz A
Department of Chemistry, Yale University, New Haven, CT 06511-8118, USA.
Chem Biol. 2000 Aug;7(8):601-10. doi: 10.1016/s1074-5521(00)00009-0.
The TATA box binding protein (TBP) is required by all three RNA polymerases for the promoter-specific initiation of transcription. All eukaryotic TBP-DNA complexes observed in crystal structures show the conserved C-terminal domain of TBP (TBPc) bound to the TATA box in a single orientation that is consistent with assembly of a preinitiation complex (PIC) possessing a unique polarity. The binding of TBP to the TATA box is believed to orient the PIC correctly on the promoter and can function as the rate-limiting step in PIC assembly. Previous work performed with TBP from Saccharomyces cerevisiae (yTBP) showed that, despite the oriented binding of eukaryotic TBP observed in crystal structures, yTBP in solution does not orient itself uniquely on the adenovirus major late promoter (AdMLP) TATA box. Instead, yTBP binds the AdMLP as a mixture of two orientational isomers that are related by a 180 degree rotation about the pseudo-dyad axis of the complex. In addition, these orientational isomers are not restricted to the 8 bp TATA box, but rather bind a distribution of sites that partially overlap the TATA box. Two members of the PIC, general transcription factor (TF) IIB and TFIIA individually enhance the orientational and axial specificity of yTBP binding to the TATA box, but fail to fix yTBP in a single orientation or a unique position on the promoter.
We used an affinity cleavage assay to explore the combined effects of TFIIA and TFIIB on the axial and orientational specificity of yTBP. Our results show that the combination of TFIIA and TFIIB affixes yTBP in virtually a single orientation as well as a unique location on the AdMLP TATA box. Ninety-five percent of the quaternary TBP-TFIIA-TFIIB-TATA complex contained yTBP bound in the orientation expected on the basis of crystallographic and genetic experiments, and more than 70% is restricted axially to the 8 bp sequence TATAAAAG.
Although yTBP itself binds to the TATA box without a high level of orientational or axial specificity, our data show that a small subset of general TFs are capable of uniquely orienting the PIC on the AdMLP. Our results, in combination with recent data concerning the pathway of PIC formation in yeast, suggest that transcription could be regulated during both early and late stages of PIC assembly by general factors (and the proteins to which they bind) that influence the position and orientation of TBP on the promoter.
三种RNA聚合酶在启动子特异性转录起始过程中均需要TATA盒结合蛋白(TBP)。在晶体结构中观察到的所有真核生物TBP-DNA复合物均显示,TBP的保守C末端结构域(TBPc)以单一方向与TATA盒结合,这与具有独特极性的起始前复合物(PIC)的组装一致。TBP与TATA盒的结合被认为可使PIC在启动子上正确定向,并可作为PIC组装中的限速步骤。先前对酿酒酵母(yTBP)的TBP进行的研究表明,尽管在晶体结构中观察到真核生物TBP存在定向结合,但溶液中的yTBP在腺病毒主要晚期启动子(AdMLP)的TATA盒上并未唯一地自我定向。相反,yTBP以两种方向异构体的混合物形式结合AdMLP,这两种异构体通过围绕复合物的假二元轴旋转180度而相互关联。此外,这些方向异构体不限于8bp的TATA盒,而是结合与TATA盒部分重叠的一系列位点。PIC的两个成员,即通用转录因子(TF)IIB和TFIIA,分别增强了yTBP与TATA盒结合的方向和轴向特异性,但未能将yTBP固定在启动子上的单一方向或独特位置。
我们使用亲和切割试验来探究TFIIA和TFIIB对yTBP轴向和方向特异性的综合影响。我们的结果表明,TFIIA和TFIIB的组合实际上将yTBP固定在单一方向以及AdMLP TATA盒上的独特位置。95%的四级TBP-TFIIA-TFIIB-TATA复合物中,yTBP的结合方向与基于晶体学和遗传学实验预期的方向一致,并且超过70%在轴向上被限制在8bp序列TATAAAAG上。
尽管yTBP本身与TATA盒结合时没有高度的方向或轴向特异性,但我们的数据表明,一小部分通用转录因子能够使PIC在AdMLP上唯一地定向。我们的结果与最近关于酵母中PIC形成途径的数据相结合,表明转录可能在PIC组装的早期和晚期阶段都受到通用因子(以及它们所结合的蛋白质)的调节,这些因子会影响TBP在启动子上的位置和方向。