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TATA 结合蛋白相关因子可增强转录激活因子对 RNA 聚合酶 II 的招募作用。

TATA-binding protein-associated factors enhance the recruitment of RNA polymerase II by transcriptional activators.

作者信息

Wu S Y, Chiang C M

机构信息

Department of Biochemistry, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106-4935, USA.

出版信息

J Biol Chem. 2001 Sep 7;276(36):34235-43. doi: 10.1074/jbc.M102463200. Epub 2001 Jul 16.

Abstract

Transcription factor (TF) IID, comprised of the TATA-binding protein (TBP) and TBP-associated factors (TAFs), is a general transcription factor required for RNA polymerase II (pol II) transcription on most eukaryotic genes. Recent findings that TAFs may not be globally required for activator-dependent transcription in vivo and in vitro and that both TAF-dependent and TAF-independent promoters are found in yeast suggest that transcriptional activation can occur through at least two different pathways, depending on the presence or absence of TAFs. Using order-of-addition and template challenge assays performed in a human cell-free transcription system reconstituted with recombinant general transcription factors (TFIIB, TBP, TFIIE, TFIIF), a recombinant general cofactor (PC4), and highly purified epitope-tagged multiprotein complexes (TFIID, TFIIH, pol II), we demonstrate that when TBP is used as the TATA-binding factor transcriptional activators such as Gal4-VP16 and human papillomavirus E2 mainly function by facilitating pol II entry to the promoter region. In contrast, when TFIID is used as the TATA-binding factor, promoter recognition by TFIID appears to be the rate-limiting step facilitated by transcriptional activators during preinitiation complex assembly. Using protein-protein pull-down and far-Western analyses, we further show that the presence of TAFs in TFIID facilitates the recruitment of pol II by transcriptional activators, thereby switching the rate-limiting step from pol II entry to promoter recognition. Our findings thus provide distinct molecular mechanisms for TAF-independent and TAF-dependent activation.

摘要

转录因子(TF)IID由TATA结合蛋白(TBP)和TBP相关因子(TAFs)组成,是大多数真核基因上RNA聚合酶II(pol II)转录所需的通用转录因子。最近的研究发现,TAFs在体内和体外的激活剂依赖性转录中可能并非全局必需,并且在酵母中发现了依赖TAF和不依赖TAF的启动子,这表明转录激活可以通过至少两种不同的途径发生,这取决于TAFs的存在与否。在一个用重组通用转录因子(TFIIB、TBP、TFIIE、TFIIF)、重组通用辅因子(PC4)和高度纯化的表位标记多蛋白复合物(TFIID、TFIIH、pol II)重构的无细胞人类转录系统中进行添加顺序和模板挑战试验,我们证明,当TBP用作TATA结合因子时,转录激活剂如Gal4-VP16和人乳头瘤病毒E2主要通过促进pol II进入启动子区域发挥作用。相反,当TFIID用作TATA结合因子时,TFIID对启动子的识别似乎是转录激活剂在起始前复合物组装过程中促进的限速步骤。通过蛋白质-蛋白质下拉和远Western分析,我们进一步表明,TFIID中TAFs的存在促进了转录激活剂对pol II的招募,从而将限速步骤从pol II进入切换为启动子识别。因此,我们的研究结果为不依赖TAF和依赖TAF的激活提供了不同的分子机制。

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