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转录延伸的基本机制及其调控。

Basic mechanisms of transcript elongation and its regulation.

作者信息

Uptain S M, Kane C M, Chamberlin M J

机构信息

Department of Molecular and Cell Biology, University of California at Berkeley 94720, USA.

出版信息

Annu Rev Biochem. 1997;66:117-72. doi: 10.1146/annurev.biochem.66.1.117.

Abstract

Ternary complexes of DNA-dependent RNA polymerase with its DNA template and nascent transcript are central intermediates in transcription. In recent years, several unusual biochemical reactions have been discovered that affect the progression of RNA polymerase in ternary complexes through various transcription units. These reactions can be signaled intrinsically, by nucleic acid sequences and the RNA polymerase, or extrinsically, by protein or other regulatory factors. These factors can affect any of these processes, including promoter proximal and promoter distal pausing in both prokaryotes and eukaryotes, and therefore play a central role in regulation of gene expression. In eukaryotic systems, at least two of these factors appear to be related to cellular transformation and human cancers. New models for the structure of ternary complexes, and for the mechanism by which they move along DNA, provide plausible explanations for novel biochemical reactions that have been observed. These models predict that RNA polymerase moves along DNA without the constant possibility of dissociation and consequent termination. A further prediction of these models is that the polymerase can move in a discontinuous or inchworm-like manner. Many direct predictions of these models have been confirmed. However, one feature of RNA chain elongation not predicted by the model is that the DNA sequence can determine whether the enzyme moves discontinuously or monotonically. In at least two cases, the encounter between the RNA polymerase and a DNA block to elongation appears to specifically induce a discontinuous mode of synthesis. These findings provide important new insights into the RNA chain elongation process and offer the prospect of understanding many significant biological regulatory systems at the molecular level.

摘要

依赖DNA的RNA聚合酶与其DNA模板及新生转录本形成的三元复合物是转录过程中的核心中间体。近年来,人们发现了几种不同寻常的生化反应,这些反应通过各种转录单元影响三元复合物中RNA聚合酶的行进。这些反应可以由核酸序列和RNA聚合酶内在发出信号,也可以由蛋白质或其他调节因子外在发出信号。这些因素可以影响这些过程中的任何一个,包括原核生物和真核生物中启动子近端和启动子远端的暂停,因此在基因表达调控中起着核心作用。在真核系统中,这些因素中至少有两个似乎与细胞转化和人类癌症有关。三元复合物的结构模型以及它们沿DNA移动的机制,为已观察到的新型生化反应提供了合理的解释。这些模型预测,RNA聚合酶沿DNA移动时不存在持续解离及随之终止的可能性。这些模型的另一个预测是,聚合酶可以以不连续或类似尺蠖的方式移动。这些模型的许多直接预测已得到证实。然而,该模型未预测到的RNA链延伸的一个特征是,DNA序列可以决定酶是不连续移动还是单调移动。在至少两种情况下,RNA聚合酶与DNA延伸障碍的相遇似乎会特异性地诱导不连续的合成模式。这些发现为RNA链延伸过程提供了重要的新见解,并为在分子水平上理解许多重要的生物调节系统带来了希望。

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