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多亚基RNA聚合酶介导的易位

Translocation by multi-subunit RNA polymerases.

作者信息

Kireeva Maria, Kashlev Mikhail, Burton Zachary F

机构信息

National Cancer Institute-Frederick, Frederick, MD 21702-1201, USA.

出版信息

Biochim Biophys Acta. 2010 May-Jun;1799(5-6):389-401. doi: 10.1016/j.bbagrm.2010.01.007. Epub 2010 Jan 25.

Abstract

DNA template and RNA/DNA hybrid movement through RNA polymerase (RNAP) is referred to as "translocation". Because nucleic acid movement is coupled to NTP loading, pyrophosphate release, and conformational changes, the precise ordering of events during bond addition is consequential. Moreover, based on several lines of experimental evidence, translocation, pyrophosphate release or an associated conformational change may determine the transcription elongation rate. In this review we discuss various models of translocation, the data supporting the hypothesis that translocation rate determines transcription elongation rate and also data that may be inconsistent with this point of view. A model of the nucleotide addition cycle accommodating available experimental data is proposed. On the basis of this model, the molecular mechanisms regulating translocation and potential routes for NTP entry are discussed.

摘要

DNA模板以及RNA/DNA杂交体通过RNA聚合酶(RNAP)的移动被称为“易位”。由于核酸移动与NTP装载、焦磷酸释放以及构象变化相耦合,因此在添加化学键过程中事件的精确顺序至关重要。此外,基于多方面的实验证据,易位、焦磷酸释放或相关的构象变化可能决定转录延伸速率。在本综述中,我们讨论了易位的各种模型、支持易位速率决定转录延伸速率这一假说的数据,以及可能与此观点不一致的数据。我们提出了一个容纳现有实验数据的核苷酸添加循环模型。基于该模型,讨论了调节易位的分子机制以及NTP进入的潜在途径。

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