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不同的人类TFIIIB活性指导RNA聚合酶III从含TATA和不含TATA的启动子进行转录。

Different human TFIIIB activities direct RNA polymerase III transcription from TATA-containing and TATA-less promoters.

作者信息

Schramm L, Pendergrast P S, Sun Y, Hernandez N

机构信息

Department of Pharmacology, State University of New York at Stony Brook, Stony Brook, New York 11794, USA.

出版信息

Genes Dev. 2000 Oct 15;14(20):2650-63. doi: 10.1101/gad.836400.

Abstract

Transcription initiation at RNA polymerase III promoters requires transcription factor IIIB (TFIIIB), an activity that binds to RNA polymerase III promoters, generally through protein-protein contacts with DNA binding factors, and directly recruits RNA polymerase III. Saccharomyces cerevisiae TFIIIB is a complex of three subunits, TBP, the TFIIB-related factor BRF, and the more loosely associated polypeptide beta("). Although human homologs for two of the TFIIIB subunits, the TATA box-binding protein TBP and the TFIIB-related factor BRF, have been characterized, a human homolog of yeast B(") has not been described. Moreover, human BRF, unlike yeast BRF, is not universally required for RNA polymerase III transcription. In particular, it is not involved in transcription from the small nuclear RNA (snRNA)-type, TATA-containing, RNA polymerase III promoters. Here, we characterize two novel activities, a human homolog of yeast B("), which is required for transcription of both TATA-less and snRNA-type RNA polymerase III promoters, and a factor equally related to human BRF and TFIIB, designated BRFU, which is specifically required for transcription of snRNA-type RNA polymerase III promoters. Together, these results contribute to the definition of the basal RNA polymerase III transcription machinery and show that two types of TFIIIB activities, with specificities for different classes of RNA polymerase III promoters, have evolved in human cells.

摘要

RNA聚合酶III启动子的转录起始需要转录因子IIIB(TFIIIB),该活性通常通过与DNA结合因子的蛋白质-蛋白质相互作用与RNA聚合酶III启动子结合,并直接招募RNA聚合酶III。酿酒酵母TFIIIB是由三个亚基组成的复合物,即TBP、TFIIB相关因子BRF和结合较松散的多肽β(β”)。尽管已对TFIIIB的两个亚基的人类同源物,即TATA盒结合蛋白TBP和TFIIB相关因子BRF进行了表征,但尚未描述酵母β”的人类同源物。此外,与酵母BRF不同,人类BRF并非RNA聚合酶III转录普遍所需。特别是,它不参与来自小核RNA(snRNA)型、含TATA的RNA聚合酶III启动子的转录。在这里,我们鉴定了两种新活性,一种是酵母β”的人类同源物,它是无TATA和snRNA型RNA聚合酶III启动子转录所必需的;另一种是与人类BRF和TFIIB同样相关的因子,命名为BRFU,它是snRNA型RNA聚合酶III启动子转录所特需的。总之,这些结果有助于确定基础RNA聚合酶III转录机制,并表明在人类细胞中已进化出对不同类别的RNA聚合酶III启动子具有特异性的两种TFIIIB活性。

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