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通过体内募集TBP刺激RNA聚合酶II转录起始。

Stimulation of RNA polymerase II transcription initiation by recruitment of TBP in vivo.

作者信息

Klages N, Strubin M

机构信息

Department of Genetics and Microbiology, University Medical Centre (CMU), Geneva, Switzerland.

出版信息

Nature. 1995 Apr 27;374(6525):822-3. doi: 10.1038/374822a0.

Abstract

Eukaryotic transcriptional activators may stimulate RNA polymerase II activity by promoting assembly of preinitiation complexes on promoters through their interactions with one or more components of the basal machinery. On the basis of its central role in initiating transcription-complex formation upon binding to the TATA box, the general transcription factor TFIID, which includes the TATA-binding protein (TBP) and several TBP-associated factors, has been implicated as a target for activators. Consistent with this idea, an increasing number of activators have been reported to bind directly to TBP. To assess the functional importance of these in vitro interactions for transcriptional regulation in vivo, we made use of a novel strategy in yeast to show that a physical interaction with TBP is sufficient for a sequence-specific DNA-binding protein to increase initiation of transcription by RNA polymerase II. These results imply that binding of TFIID to promoter elements is a limiting step in transcription complex assembly in vivo.

摘要

真核转录激活因子可通过与基础转录机制的一个或多个组分相互作用,促进启动子上起始前复合物的组装,从而刺激RNA聚合酶II的活性。通用转录因子TFIID包括TATA结合蛋白(TBP)和几个TBP相关因子,由于其在结合TATA框后启动转录复合物形成过程中的核心作用,已被认为是激活因子的作用靶点。与这一观点一致,越来越多的激活因子被报道可直接与TBP结合。为了评估这些体外相互作用对体内转录调控的功能重要性,我们在酵母中采用了一种新策略,以表明与TBP的物理相互作用足以使序列特异性DNA结合蛋白增加RNA聚合酶II介导的转录起始。这些结果表明,TFIID与启动子元件的结合是体内转录复合物组装的一个限制步骤。

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