Abrahem Abrahem, Pelchat Martin
Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, K1H 8M5, Canada.
Nucleic Acids Res. 2008 Sep;36(16):5201-11. doi: 10.1093/nar/gkn501. Epub 2008 Aug 5.
Although RNA polymerases (RNAPs) are able to use RNA as template, it is unknown how they recognize RNA promoters. In this study, we used an RNA fragment derived from the hepatitis delta virus (HDV) genome as a model to investigate the recognition of RNA promoters by RNAP II. Inhibition of the transcription reaction using an antibody specific to the largest subunit of RNAP II and the direct binding of purified RNAP II to the RNA promoter confirmed the involvement of RNAP II in the reaction. RNA affinity chromatography established that an active RNAP II preinitiation complex forms on the RNA promoter and indicated that this complex contains the core RNAP II subunit and the general transcription factors TFIIA, TFIIB, TFIID, TFIIE, TFIIF, TFIIH and TFIIS. Binding assays demonstrated the direct binding of the TATA-binding protein and suggested that this protein is required to nucleate the RNAP II complex on the RNA promoter. Our findings provide a better understanding of the events leading to RNA promoter recognition by RNAP II.
尽管RNA聚合酶(RNAPs)能够以RNA为模板,但它们如何识别RNA启动子尚不清楚。在本研究中,我们使用源自丁型肝炎病毒(HDV)基因组的RNA片段作为模型,来研究RNAP II对RNA启动子的识别。使用针对RNAP II最大亚基的特异性抗体抑制转录反应,以及纯化的RNAP II与RNA启动子的直接结合,证实了RNAP II参与了该反应。RNA亲和层析表明,在RNA启动子上形成了活性RNAP II预起始复合物,并表明该复合物包含核心RNAP II亚基以及通用转录因子TFIIA、TFIIB、TFIID、TFIIE、TFIIF、TFIIH和TFIIS。结合试验证明了TATA结合蛋白的直接结合,并表明该蛋白是在RNA启动子上使RNAP II复合物成核所必需的。我们的研究结果为导致RNAP II识别RNA启动子的事件提供了更好的理解。