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转录保真度和DNA损伤诱导的转录诱变的分子基础。

Molecular basis of transcriptional fidelity and DNA lesion-induced transcriptional mutagenesis.

作者信息

Xu Liang, Da Linati, Plouffe Steven W, Chong Jenny, Kool Eric, Wang Dong

机构信息

Skaggs School of Pharmacy and Pharmaceutical Science, University of California San Diego, La Jolla, CA 92093-0625, United States.

Department of Chemistry, Stanford University, Stanford, CA 94305-5080, United States.

出版信息

DNA Repair (Amst). 2014 Jul;19:71-83. doi: 10.1016/j.dnarep.2014.03.024. Epub 2014 Apr 21.

Abstract

Maintaining high transcriptional fidelity is essential for life. Some DNA lesions lead to significant changes in transcriptional fidelity. In this review, we will summarize recent progress towards understanding the molecular basis of RNA polymerase II (Pol II) transcriptional fidelity and DNA lesion-induced transcriptional mutagenesis. In particular, we will focus on the three key checkpoint steps of controlling Pol II transcriptional fidelity: insertion (specific nucleotide selection and incorporation), extension (differentiation of RNA transcript extension of a matched over mismatched 3'-RNA terminus), and proofreading (preferential removal of misincorporated nucleotides from the 3'-RNA end). We will also discuss some novel insights into the molecular basis and chemical perspectives of controlling Pol II transcriptional fidelity through structural, computational, and chemical biology approaches.

摘要

维持高转录保真度对生命至关重要。一些DNA损伤会导致转录保真度发生显著变化。在本综述中,我们将总结在理解RNA聚合酶II(Pol II)转录保真度的分子基础以及DNA损伤诱导的转录诱变方面的最新进展。特别地,我们将聚焦于控制Pol II转录保真度的三个关键检查点步骤:插入(特定核苷酸的选择与掺入)、延伸(匹配的3'-RNA末端与错配的3'-RNA末端在RNA转录本延伸上的区分)和校对(从3'-RNA末端优先去除错掺入的核苷酸)。我们还将讨论通过结构、计算和化学生物学方法控制Pol II转录保真度的分子基础和化学视角的一些新见解。

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本文引用的文献

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