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噬菌体T4 AsiA对大肠杆菌RNA聚合酶的抑制作用。

Inhibition of Escherichia coli RNA polymerase by bacteriophage T4 AsiA.

作者信息

Severinova E, Severinov K, Darst S A

机构信息

Rockefeller University, New York, NY 10021, USA.

出版信息

J Mol Biol. 1998 May 29;279(1):9-18. doi: 10.1006/jmbi.1998.1742.

Abstract

The 10 kDa bacteriophage T4 antisigma protein AsiA binds the Escherichia coli RNA polymerase promoter specificity subunit, sigma 70, with high affinity and inhibits its transcription activity. AsiA binds to sigma 70 primarily through an interaction with sigma 70 conserved region 4.2, which has also been implicated in sequence-specific recognition of the -35 consensus promoter element. Here we show that AsiA forms a stable ternary complex with core RNA polymerase (RNAP) and sigma 70 and thus does not inhibit sigma 70 activity by preventing its binding to core RNAP. We investigated the effect of AsiA on open promoter complex formation and abortive initiation at two -10/-35 type promoters and two "extended -10" promoters. Our results indicate that the binding of AsiA to sigma 70 and the interaction of sigma 70 region 4.2 with the -35 consensus promoter element of -10/-35 promoters is mutually exclusive. In contrast, AsiA has much less effect on open promoter complex formation and abortive initiation from extended -10 promoters, which lack a -35 consensus element and do not require sigma 70 conserved region 4.2. From these results we conclude that T4 AsiA inhibits E. coli RNAP sigma 70 holoenzyme transcription at -10/-35 promoters by interfering with the required interaction between sigma 70 conserved region 4.2 and the -35 consensus promoter element.

摘要

10千道尔顿的噬菌体T4抗σ蛋白AsiA以高亲和力结合大肠杆菌RNA聚合酶启动子特异性亚基σ70,并抑制其转录活性。AsiA主要通过与σ70保守区域4.2相互作用而结合到σ70上,该区域也与-35共有启动子元件的序列特异性识别有关。在此我们表明,AsiA与核心RNA聚合酶(RNAP)和σ70形成稳定的三元复合物,因此并非通过阻止σ70与核心RNAP结合来抑制其活性。我们研究了AsiA对两个-10/-35型启动子和两个“延伸-10”启动子处开放启动子复合物形成及流产起始的影响。我们的结果表明,AsiA与σ70的结合以及σ70区域4.2与-10/-35启动子的-35共有启动子元件的相互作用是相互排斥的。相反,AsiA对缺乏-35共有元件且不需要σ70保守区域4.2的延伸-10启动子处的开放启动子复合物形成及流产起始影响小得多。从这些结果我们得出结论,T4 AsiA通过干扰σ70保守区域4.2与-35共有启动子元件之间的必要相互作用,抑制-10/-35启动子处大肠杆菌RNAP σ70全酶的转录。

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