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转录保真度突变体的分离与鉴定

Isolation and characterization of transcription fidelity mutants.

作者信息

Strathern Jeffrey N, Jin Ding Jun, Court Donald L, Kashlev Mikhail

机构信息

Gene Regulation and Chromosome Biology Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702, USA.

出版信息

Biochim Biophys Acta. 2012 Jul;1819(7):694-9. doi: 10.1016/j.bbagrm.2012.02.005. Epub 2012 Feb 16.

Abstract

Accurate transcription is an essential step in maintaining genetic information. Error-prone transcription has been proposed to contribute to cancer, aging, adaptive mutagenesis, and mutagenic evolution of retroviruses and retrotransposons. The mechanisms controlling transcription fidelity and the biological consequences of transcription errors are poorly understood. Because of the transient nature of mRNAs and the lack of reliable experimental systems, the identification and characterization of defects that increase transcription errors have been particularly challenging. In this review we describe novel genetic screens for the isolation of fidelity mutants in both Saccharomyces cerevisiae and Escherichia coli RNA polymerases. We obtained and characterized two distinct classes of mutants altering NTP misincorporation and transcription slippage both in vivo and in vitro. Our study not only validates the genetic schemes for the isolation of RNA polymerase mutants that alter fidelity, but also sheds light on the mechanism of transcription accuracy. This article is part of a Special Issue entitled: Chromatin in time and space.

摘要

准确转录是维持遗传信息的关键步骤。有人提出易出错的转录会导致癌症、衰老、适应性诱变以及逆转录病毒和逆转座子的诱变进化。目前对控制转录保真度的机制以及转录错误的生物学后果了解甚少。由于mRNA的瞬时性质以及缺乏可靠的实验系统,识别和表征增加转录错误的缺陷尤其具有挑战性。在这篇综述中,我们描述了用于分离酿酒酵母和大肠杆菌RNA聚合酶中保真度突变体的新型遗传筛选方法。我们获得并表征了两类不同的突变体,它们在体内和体外均改变了NTP错掺入和转录滑动。我们的研究不仅验证了用于分离改变保真度的RNA聚合酶突变体的遗传方案,还揭示了转录准确性的机制。本文是名为“时空染色质”的特刊的一部分。

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