Zhang Dong-Yi, Carson Daniel J, Ma Jun
Division of Developmental Biology, Children's Hospital Research Foundation, 3333 Burnet Avenue, Cincinnati, OH 45229, USA.
Nucleic Acids Res. 2002 Jul 15;30(14):3078-85. doi: 10.1093/nar/gkf422.
Previous studies have established a critical role of both TFIIB and RNA polymerase II (RNAPII) in start site selection in the yeast Saccharomyces cerevisiae. However, it remains unclear how the TFIIB-RNAPII interaction impacts on this process since such an interaction can potentially influence both preinitiation complex (PIC) stability and conformation. In this study, we further investigate the role of TFIIB in start site selection by characterizing our newly generated TFIIB mutants, two of which exhibit a novel upstream shift of start sites in vivo. We took advantage of an artificial recruitment system in which an RNAPII holoenzyme component is covalently linked to a DNA-binding domain for more direct and stable recruitment. We show that TFIIB mutations can exert their effects on start site selection in such an artificial recruitment system even though it has a relaxed requirement for TFIIB. We further show that these TFIIB mutants have normal affinity for RNAPII and do not alter the promoter melting/scanning step. Finally, we show that overexpressing the genetically isolated TFIIB mutant E62K, which has a reduced affinity for RNAPII, can correct its start site selection defect. We discuss a model in which the TFIIB-RNAPII interaction controls the start site selection process by influencing the conformation of PIC prior to or during PIC assembly, as opposed to PIC stability.
先前的研究已经证实,转录因子IIB(TFIIB)和RNA聚合酶II(RNAPII)在酿酒酵母起始位点选择过程中都起着关键作用。然而,TFIIB与RNAPII之间的相互作用如何影响这一过程仍不清楚,因为这种相互作用可能会潜在地影响起始前复合物(PIC)的稳定性和构象。在本研究中,我们通过对新构建的TFIIB突变体进行表征,进一步探究了TFIIB在起始位点选择中的作用,其中两个突变体在体内表现出起始位点的新型上游移位。我们利用了一种人工招募系统,在该系统中,RNAPII全酶组分与一个DNA结合结构域共价连接,以实现更直接和稳定的招募。我们发现,尽管该人工招募系统对TFIIB的要求较为宽松,但TFIIB突变体仍能在此系统中对起始位点选择产生影响。我们进一步表明,这些TFIIB突变体对RNAPII具有正常的亲和力,并且不会改变启动子解链/扫描步骤。最后,我们发现过表达对RNAPII亲和力降低但经基因分离的TFIIB突变体E62K,可以纠正其起始位点选择缺陷。我们讨论了一个模型,其中TFIIB-RNAPII相互作用通过在PIC组装之前或期间影响PIC的构象来控制起始位点选择过程,而不是通过影响PIC的稳定性。