Kugel J F, Goodrich J A
Department of Chemistry and Biochemistry, University of Colorado at Boulder, Boulder, Colorado 80309-0215, USA.
J Biol Chem. 2000 Dec 22;275(51):40483-91. doi: 10.1074/jbc.M006401200.
Eukaryotic mRNA synthesis is a highly regulated process involving numerous proteins acting in concert with RNA polymerase II to set levels of transcription from individual promoters. The transcription reaction consists of multiple steps beginning with preinitiation complex formation and ending in the production of a full-length primary transcript. We used pre-steady-state approaches to study the steps of human mRNA transcription at the adenovirus major late promoter in a minimal in vitro transcription system. These kinetic studies revealed an early transition in RNA polymerase II transcription, termed escape commitment, that occurs after initiation and prior to promoter escape. Escape commitment is rapid and is characterized by sensitivity to competitor DNA. Upon completion of escape commitment, ternary complexes are resistant to challenge by competitor DNA and slowly proceed forward through promoter escape. Escape commitment is stimulated by transcription factors TFIIE and TFIIH. We measured forward and reverse rate constants for discrete steps in transcription and present a kinetic model for the mechanism of RNA polymerase II transcription that describes five distinct steps (preinitiation complex formation, initiation, escape commitment, promoter escape, and transcript elongation) and clearly shows promoter escape is rate-limiting in this system.
真核生物mRNA合成是一个高度调控的过程,涉及众多蛋白质与RNA聚合酶II协同作用,以设定各个启动子的转录水平。转录反应由多个步骤组成,从起始前复合物形成开始,到全长初级转录本的产生结束。我们使用预稳态方法,在一个最小的体外转录系统中研究腺病毒主要晚期启动子处人类mRNA转录的步骤。这些动力学研究揭示了RNA聚合酶II转录过程中的一个早期转变,称为逃逸承诺,它发生在起始后和启动子逃逸之前。逃逸承诺迅速,其特点是对竞争DNA敏感。逃逸承诺完成后,三元复合物对竞争DNA的挑战具有抗性,并缓慢地通过启动子逃逸向前推进。转录因子TFIIE和TFIIH刺激逃逸承诺。我们测量了转录中离散步骤的正向和反向速率常数,并提出了一个RNA聚合酶II转录机制的动力学模型,该模型描述了五个不同的步骤(起始前复合物形成、起始、逃逸承诺、启动子逃逸和转录本延伸),并清楚地表明启动子逃逸在该系统中是限速步骤。