Wang Y, Stumph W E
Department of Chemistry, San Diego State University, CA 92182-1030, USA.
Proc Natl Acad Sci U S A. 1995 Sep 12;92(19):8606-10. doi: 10.1073/pnas.92.19.8606.
The TATA box sequence in eukaryotes is located about 25 bp upstream of many genes transcribed by RNA polymerase II (Pol II) and some genes transcribed by RNA polymerase III (Pol III). The TATA box is recognized in a sequence-specific manner by the TATA box-binding protein (TBP), an essential factor involved in the initiation of transcription by all three eukaryotic RNA polymerases. We have investigated the recognition of the TATA box by the Pol II and Pol III basal transcription machinery and its role in establishing the RNA polymerase specificity of the promoter. Artificial templates were constructed that contained a canonical TATA box as the sole promoter element but differed in the orientation of the 8-bp TATA box sequence. As expected, Pol II initiated transcription in unfractionated nuclear extracts downstream of the "forward" TATA box. In distinct contrast, transcription that initiated downstream of the "reverse" TATA box was carried out specifically by Pol III. Importantly, this effect was observed regardless of the source of the DNA either upstream or downstream of the TATA sequence. These findings suggest that TBP may bind in opposite orientations on Pol II and Pol III promoters and that opposite, yet homologous, surfaces of TBP may be utilized by the Pol II and Pol III basal machinery for the initiation of transcription.
真核生物中的TATA框序列位于许多由RNA聚合酶II(Pol II)转录的基因以及一些由RNA聚合酶III(Pol III)转录的基因上游约25个碱基对处。TATA框以序列特异性方式被TATA框结合蛋白(TBP)识别,TBP是所有三种真核生物RNA聚合酶转录起始过程中涉及的必需因子。我们研究了Pol II和Pol III基础转录机制对TATA框的识别及其在建立启动子RNA聚合酶特异性中的作用。构建了人工模板,其包含一个典型的TATA框作为唯一的启动子元件,但8个碱基对的TATA框序列方向不同。正如预期的那样,Pol II在未分级的核提取物中“正向”TATA框下游启动转录。截然不同的是,在“反向”TATA框下游启动的转录是由Pol III特异性进行的。重要的是,无论TATA序列上游还是下游的DNA来源如何,都观察到了这种效应。这些发现表明,TBP可能以相反的方向结合在Pol II和Pol III启动子上,并且Pol II和Pol III基础机制可能利用TBP相反但同源的表面来启动转录。