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Isolation and characterization of transcription fidelity mutants

机译:转录保真突变体的分离与鉴定

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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.
机译:准确的转录是维持遗传信息的重要步骤。已提出易错转录有助于逆转录病毒和逆转座子的癌变,衰老,适应性诱变和诱变进化。控制转录保真度的机制和转录错误的生物学后果知之甚少。由于mRNA的瞬态性质和缺乏可靠的实验系统,增加转录错误的缺陷的鉴定和表征一直具有挑战性。在这篇综述中,我们描述了两种分离保真突变体的新型遗传筛选。酿酒酵母和酵母。大肠杆菌RNA聚合酶。我们获得并表征了两种独特的突变体,分别改变了NTP错误掺入和转录滑动。体内和。体外。我们的研究不仅验证了可改变保真度的RNA聚合酶突变体的分离遗传方案,而且还阐明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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