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激活缺陷型TBP突变对酵母转录起始的影响。

Effects of activation-defective TBP mutations on transcription initiation in yeast.

作者信息

Kim T K, Hashimoto S, Kelleher R J, Flanagan P M, Kornberg R D, Horikoshi M, Roeder R G

机构信息

Laboratory of Biochemistry and Molecular Biology, Rockefeller University, New York, New York 10021.

出版信息

Nature. 1994 May 19;369(6477):252-5. doi: 10.1038/369252a0.

Abstract

Transcription initiation by RNA polymerase II is effected by an ordered series of general factor interactions with core promoter elements (leading to basal activity) and further regulated by gene-specific factors acting from distal elements. Both the general factor TFIID (refs 2,3), including the constituent TBP (TATA-binding polypeptide) and associated factors, and the interacting factor TFIIB (refs 9-11) have been implicated as targets for various activators. Towards an understanding of the basis for activator function, including the multiplicity of TBP interactions, we have now identified mutations in yeast TBP that selectively block activator (GAL4-VP16)-dependent but not basal transcription. We further show an effect of GAL4-VP16 on TFIIB recruitment to early preinitiation complexes, and that recruitment is disrupted by TBP mutations that impair its interactions with VP16 (L114K), TFIIB (L189K) or an unidentified component (K211L). Thus, GAL4-VP16 function seems to involve both direct interactions with TBP and a corresponding induction (or stabilization) of an activation-specific TBP-TFIIB-promoter complex.

摘要

RNA聚合酶II介导的转录起始由一系列与核心启动子元件的通用因子相互作用实现(导致基础活性),并由作用于远端元件的基因特异性因子进一步调控。通用因子TFIID(参考文献2,3),包括组成成分TBP(TATA结合多肽)和相关因子,以及相互作用因子TFIIB(参考文献9 - 11)均被认为是各种激活剂的作用靶点。为了理解激活剂功能的基础,包括TBP相互作用的多样性,我们现已在酵母TBP中鉴定出一些突变,这些突变选择性地阻断激活剂(GAL4 - VP16)依赖的转录,但不影响基础转录。我们进一步表明GAL4 - VP16对TFIIB募集到早期起始前复合物有影响,并且这种募集会被损害其与VP16(L114K)、TFIIB(L189K)或一个未鉴定成分(K211L)相互作用的TBP突变所破坏。因此,GAL4 - VP16的功能似乎既涉及与TBP的直接相互作用,也涉及激活特异性TBP - TFIIB - 启动子复合物的相应诱导(或稳定)。

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