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多组基础因子启动RNA聚合酶II介导的转录。

Multiple sets of basal factors initiate transcription by RNA polymerase II.

作者信息

Parvin J D, Shykind B M, Meyers R E, Kim J, Sharp P A

机构信息

Department of Biology, Massachusetts Institute of Technology, Cambridge 02139-4307.

出版信息

J Biol Chem. 1994 Jul 15;269(28):18414-21.

PMID:8034589
Abstract

The minimal requirements for transcription initiation from supercoiled templates were determined for the two major forms of TATA-binding factors found in cell extracts, the 300-kDa B-TFIID and the 1000-kDa D-TFIID complexes. As had been observed for the TATA-binding protein (TBP) subunit (Parvin and Sharp, 1993), transcription from the IgH promoter minimally requires TFIID activity plus TFIIB and RNA polymerase II. This minimal reaction is only active on negatively supercoiled template DNA. In contrast, the supercoiled templates encoding the adenovirus major late promoter (MLP), or several other promoters, require the addition of TFIIF to the minimal reaction. Further addition of TFIIE and TFIIH boosts the level of transcription from these latter promoters but is not required. In contrast to the complete reaction on linear template, transcription from supercoiled IgH or MLP templates does not require the hydrolysis of the beta-gamma bond of ATP. Fourteen different core promoters were compared in complete and minimal basal transcription reactions reconstituted with one of the three TATA activities: TBP, B-TFIID, and D-TFIID. Of these 14 promoters, only the IgH was active in the absence of TFIIF, and the other promoters demonstrated different levels of transcription depending on which basal factors were present in reaction. It is proposed that a significant level of basal transcription only requires a minimal set of factors, and stimulation by upstream activators may in part be mediated by the inclusion of additional basal factors into the initiation reaction.

摘要

针对细胞提取物中发现的两种主要形式的TATA结合因子,即300 kDa的B-TFIID和1000 kDa的D-TFIID复合物,确定了从超螺旋模板起始转录的最低要求。正如TATA结合蛋白(TBP)亚基所观察到的那样(Parvin和Sharp,1993),从IgH启动子转录最低需要TFIID活性加上TFIIB和RNA聚合酶II。这种最小反应仅在负超螺旋模板DNA上有活性。相比之下,编码腺病毒主要晚期启动子(MLP)或其他几个启动子的超螺旋模板,在最小反应中需要添加TFIIF。进一步添加TFIIE和TFIIH可提高这些后一种启动子的转录水平,但并非必需。与线性模板上的完整反应不同,从超螺旋IgH或MLP模板转录不需要ATP的β-γ键水解。在用三种TATA活性之一(TBP、B-TFIID和D-TFIID)重建的完整和最小基础转录反应中,比较了14种不同的核心启动子。在这14种启动子中,只有IgH在没有TFIIF的情况下有活性,其他启动子根据反应中存在哪些基础因子表现出不同水平的转录。有人提出,显著水平的基础转录仅需要一组最小的因子,上游激活剂的刺激可能部分是通过将额外的基础因子纳入起始反应来介导的。

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