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RNA 聚合酶 III 转录调控元件:主题与变奏。

RNA polymerase III transcription control elements: themes and variations.

机构信息

Dipartimento di Biochimica e Biologia Molecolare, Università degli Studi di Parma, Parco Area delle Scienze 23/A, 43124 Parma, Italy.

出版信息

Gene. 2012 Feb 10;493(2):185-94. doi: 10.1016/j.gene.2011.06.015. Epub 2011 Jun 25.

DOI:10.1016/j.gene.2011.06.015
PMID:21712079
Abstract

Eukaryotic genomes are punctuated by a multitude of tiny genetic elements, that share the property of being recognized and transcribed by the RNA polymerase (Pol) III machinery to produce a variety of small, abundant non-protein-coding (nc) RNAs (tRNAs, 5S rRNA, U6 snRNA and many others). The highly selective, efficient and localized action of Pol III at its minute genomic targets is made possible by a handful of cis-acting regulatory elements, located within the transcribed region (where they are bound by the multisubunit assembly factor TFIIIC) and/or upstream of the transcription start site. Most of them participate directly or indirectly in the ultimate recruitment of TFIIIB, a key multiprotein initiation factor able to direct, once assembled, multiple transcription cycles by Pol III. But the peculiar efficiency and selectivity of Pol III transcription also depends on its ability to recognize very simple and precisely positioned termination signals. Studies in the last few years have significantly expanded the set of known Pol III-associated loci in genomes and, concomitantly, have revealed unexpected features of Pol III cis-regulatory elements in terms of variety, function, genomic location and potential contribution to transcriptome complexity. Here we review, in a historical perspective, well established and newly acquired knowledge about Pol III transcription control elements, with the aim of providing a useful reference for future studies of the Pol III system, which we anticipate will be numerous and intriguing for years to come.

摘要

真核生物基因组中存在大量微小的遗传元件,这些元件具有被 RNA 聚合酶 (Pol) III 识别和转录的特性,从而产生多种小而丰富的非蛋白编码 (nc) RNA(tRNA、5S rRNA、U6 snRNA 等)。Pol III 在其微小的基因组靶标上进行高度选择性、高效和局部作用,这要归功于少数顺式作用的调节元件,这些元件位于转录区域内(在那里它们被多亚基组装因子 TFIIIC 结合)和/或转录起始位点的上游。它们中的大多数直接或间接参与 TFIIIB 的最终募集,TFIIIB 是一种关键的多蛋白起始因子,一旦组装,就能通过 Pol III 指导多个转录循环。但是,Pol III 转录的特殊效率和选择性也取决于它识别非常简单且位置精确的终止信号的能力。在过去几年中,对 Pol III 相关基因座的研究显著扩展了基因组中已知的 Pol III 相关基因座的集合,同时,也揭示了 Pol III 顺式调节元件在多样性、功能、基因组位置和对转录组复杂性的潜在贡献方面的意外特征。本文从历史角度回顾了 Pol III 转录调控元件的成熟和新获得的知识,旨在为 Pol III 系统的未来研究提供有用的参考,我们预计未来几年内将会有大量且有趣的研究。

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RNA polymerase III transcription control elements: themes and variations.RNA 聚合酶 III 转录调控元件:主题与变奏。
Gene. 2012 Feb 10;493(2):185-94. doi: 10.1016/j.gene.2011.06.015. Epub 2011 Jun 25.
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Transcription factor TFIIIB and transcription by RNA polymerase III.转录因子TFIIIB与RNA聚合酶III介导的转录
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p53 represses RNA polymerase III transcription by targeting TBP and inhibiting promoter occupancy by TFIIIB.p53通过靶向TBP并抑制TFIIIB与启动子的结合来抑制RNA聚合酶III转录。
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