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转录激活因子II 250:一个转录工具箱

TAF(II)250: a transcription toolbox.

作者信息

Wassarman D A, Sauer F

机构信息

National Institutes of Health, National Institute of Child Health and Human Development, Cell Biology and Metabolism Branch, Bethesda, MD 20892, USA.

出版信息

J Cell Sci. 2001 Aug;114(Pt 16):2895-902. doi: 10.1242/jcs.114.16.2895.

Abstract

Activation of RNA-polymerase-II-dependent transcription involves conversion of signals provided by gene-specific activator proteins into the synthesis of messenger RNA. This conversion requires dynamic structural changes in chromatin and assembly of general transcription factors (GTFs) and RNA polymerase II at core promoter sequence elements surrounding the transcription start site of genes. One hallmark of transcriptional activation is the interaction of DNA-bound activators with coactivators such as the TATA-box binding protein (TBP)-associated factors (TAF(II)s) within the GTF TFIID. TAF(II)250 possesses a variety of activities that are likely to contribute to the initial steps of RNA polymerase II transcription. TAF(II)250 is a scaffold for assembly of other TAF(II)s and TBP into TFIID, TAF(II)250 binds activators to recruit TFIID to particular promoters, TAF(II)250 regulates binding of TBP to DNA, TAF(II)250 binds core promoter initiator elements, TAF(II)250 binds acetylated lysine residues in core histones, and TAF(II)250 possesses protein kinase, ubiquitin-activating/conjugating and acetylase activities that modify histones and GTFs. We speculate that these activities achieve two goals--(1) they aid in positioning and stabilizing TFIID at particular promoters, and (2) they alter chromatin structure at the promoter to allow assembly of GTFs--and we propose a model for how TAF(II)250 converts activation signals into active transcription.

摘要

RNA聚合酶II依赖性转录的激活涉及将基因特异性激活蛋白提供的信号转化为信使RNA的合成。这种转化需要染色质的动态结构变化以及通用转录因子(GTF)和RNA聚合酶II在基因转录起始位点周围的核心启动子序列元件处的组装。转录激活的一个标志是DNA结合的激活剂与共激活剂的相互作用,例如GTF TFIID中的TATA框结合蛋白(TBP)相关因子(TAF(II)s)。TAF(II)250具有多种活性,可能有助于RNA聚合酶II转录的初始步骤。TAF(II)250是将其他TAF(II)s和TBP组装成TFIID的支架,TAF(II)250结合激活剂以将TFIID募集到特定启动子,TAF(II)250调节TBP与DNA的结合,TAF(II)250结合核心启动子起始元件,TAF(II)250结合核心组蛋白中的乙酰化赖氨酸残基,并且TAF(II)250具有修饰组蛋白和GTF的蛋白激酶、泛素激活/缀合和乙酰转移酶活性。我们推测这些活性实现了两个目标——(1)它们有助于在特定启动子处定位和稳定TFIID,以及(2)它们改变启动子处的染色质结构以允许GTF的组装——并且我们提出了一个关于TAF(II)250如何将激活信号转化为活性转录的模型。

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