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利用纯化成分在体外重建酵母RNA聚合酶I转录。基础转录不需要TATA结合蛋白。

Reconstitution of yeast RNA polymerase I transcription in vitro from purified components. TATA-binding protein is not required for basal transcription.

作者信息

Keener J, Josaitis C A, Dodd J A, Nomura M

机构信息

Department of Biological Chemistry, University of California, Irvine, California 92697-1700, USA.

出版信息

J Biol Chem. 1998 Dec 11;273(50):33795-802. doi: 10.1074/jbc.273.50.33795.

Abstract

Five purified protein components, RNA polymerase I, Rrn3p, core factor, TBP (TATA-binding protein), and upstream activation factor, are sufficient for high level transcription in vitro from the Saccharomyces cerevisiae rDNA promoter. Rrn3p and pol I form a complex in solution that is active in specific initiation. Three protein components, pol I, Rrn3p, and core factor, and promoter sequence to -38, suffice for basal transcription. Unlike pol II and pol III, yeast pol I basal transcription does not require TBP. Instead, TBP, upstream activation factor, and the upstream element of the promoter together stimulate pol I basal transcription to a fully activated level. The role of TBP in pol I transcription is fundamentally different from its role in pol II or pol III transcription.

摘要

五种纯化的蛋白质组分,即RNA聚合酶I、Rrn3p、核心因子、TBP(TATA结合蛋白)和上游激活因子,足以在体外实现从酿酒酵母rDNA启动子进行的高水平转录。Rrn3p和聚合酶I在溶液中形成一个在特异性起始过程中具有活性的复合物。三种蛋白质组分,即聚合酶I、Rrn3p和核心因子,以及至-38位的启动子序列,足以进行基础转录。与聚合酶II和聚合酶III不同,酵母聚合酶I的基础转录不需要TBP。相反,TBP、上游激活因子和启动子的上游元件共同将聚合酶I的基础转录刺激到完全激活的水平。TBP在聚合酶I转录中的作用与其在聚合酶II或聚合酶III转录中的作用根本不同。

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