热噬菌体转录调节剂研究揭示RNA聚合酶启动子特异性开关的分子基础。

Bacteriophage Pub Date : 2014-05-29 eCollection Date: 2014-01-01 DOI:10.4161/bact.29399
Konstantin Severinov, Leonid Minakhin, Shun-Ichi Sekine, Anna Lopatina, Shigeyuki Yokoyama
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引用次数: 2

摘要

转录起始是基因表达调控的中心点。了解转录调控的分子机制,最终需要从结构上理解转录因子与转录酶dna依赖性RNA聚合酶(RNA -dependent RNA polymerase, RNAP)结合的后果。我们最近确定了由Thermus噬菌体编码的转录因子gp39和Thermus RNAP全酶之间的复合物的结构。在这篇原始出版物的附录中,我们强调了解释gp39作为RNAP特异性开关的能力的结构见解,该开关抑制来自主要细菌启动子的转录起始,同时允许来自次要启动子类的转录继续。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Molecular basis of RNA polymerase promoter specificity switch revealed through studies of <i>Thermus</i> bacteriophage transcription regulator.

Molecular basis of RNA polymerase promoter specificity switch revealed through studies of <i>Thermus</i> bacteriophage transcription regulator.

Molecular basis of RNA polymerase promoter specificity switch revealed through studies of <i>Thermus</i> bacteriophage transcription regulator.

Molecular basis of RNA polymerase promoter specificity switch revealed through studies of Thermus bacteriophage transcription regulator.

Transcription initiation is the central point of gene expression regulation. Understanding of molecular mechanism of transcription regulation requires, ultimately, the structural understanding of consequences of transcription factors binding to DNA-dependent RNA polymerase (RNAP), the enzyme of transcription. We recently determined a structure of a complex between transcription factor gp39 encoded by a Thermus bacteriophage and Thermus RNAP holoenzyme. In this addendum to the original publication, we highlight structural insights that explain the ability of gp39 to act as an RNAP specificity switch which inhibits transcription initiation from a major class of bacterial promoters, while allowing transcription from a minor promoter class to continue.

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