Arndt K M, Ricupero-Hovasse S, Winston F
Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.
EMBO J. 1995 Apr 3;14(7):1490-7. doi: 10.1002/j.1460-2075.1995.tb07135.x.
The TATA box binding protein (TBP) plays a central and essential role in transcription initiation. At TATA box-containing genes transcribed by RNA polymerase II, TBP binds to the promoter and initiates the assembly of a multiprotein preinitiation complex. Several studies have suggested that binding of TBP to the TATA box is an important regulatory step in transcription initiation in vitro. To determine whether TBP is a target of regulatory factors in vivo, we performed a genetic screen in yeast for TBP mutants defective in activated transcription. One class of TBP mutants identified in this screen comprises inositol auxotrophs that are also defective in using galactose as a carbon source. These phenotypes are due to promoter-specific defects in transcription initiation that are governed by the upstream activating sequence (UAS) and apparently not by the sequence of the TATA element. The finding that these TBP mutants are severely impaired in DNA binding in vitro suggests that transcription initiation at certain genes is regulated at the level of TATA box binding by TBP in vivo.
TATA盒结合蛋白(TBP)在转录起始过程中发挥着核心且关键的作用。在由RNA聚合酶II转录的含TATA盒的基因中,TBP与启动子结合并启动多蛋白预起始复合物的组装。多项研究表明,TBP与TATA盒的结合是体外转录起始过程中的一个重要调控步骤。为了确定TBP在体内是否为调控因子的作用靶点,我们在酵母中针对激活转录存在缺陷的TBP突变体进行了遗传筛选。在此筛选中鉴定出的一类TBP突变体包括肌醇营养缺陷型,它们在利用半乳糖作为碳源方面也存在缺陷。这些表型是由于转录起始过程中启动子特异性缺陷所致,这些缺陷由上游激活序列(UAS)控制,显然不是由TATA元件的序列所决定。这些TBP突变体在体外DNA结合方面严重受损这一发现表明,体内某些基因的转录起始在TBP与TATA盒结合的水平受到调控。