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通过Fis蛋白介导的DNA结构传递机制从稳定RNA启动子激活转录起始。

Activation of transcription initiation from a stable RNA promoter by a Fis protein-mediated DNA structural transmission mechanism.

作者信息

Opel Michael L, Aeling Kimberly A, Holmes Walter M, Johnson Reid C, Benham Craig J, Hatfield G Wesley

机构信息

Department of Microbiology and Molecular Genetics, College of Medicine, University of California, Irvine, CA 92697, USA.

出版信息

Mol Microbiol. 2004 Jul;53(2):665-74. doi: 10.1111/j.1365-2958.2004.04147.x.

Abstract

The leuV operon of Escherichia coli encodes three of the four genes for the tRNA1Leu isoacceptors. Transcription from this and other stable RNA promoters is known to be affected by a cis-acting UP element and by Fis protein interactions with the carboxyl-terminal domain of the alpha-subunits of RNA polymerase. In this report, we suggest that transcription from the leuV promoter also is activated by a Fis-mediated, DNA supercoiling-dependent mechanism similar to the IHF-mediated mechanism described previously for the ilvP(G) promoter (S. D. Sheridan et al., 1998, J Biol Chem 273: 21298-21308). We present evidence that Fis binding results in the translocation of superhelical energy from the promoter-distal portion of a supercoiling-induced DNA duplex destabilized (SIDD) region to the promoter-proximal portion of the leuV promoter that is unwound within the open complex. A mutant Fis protein, which is defective in contacting the carboxyl-terminal domain of the alpha-subunits of RNA polymerase, remains competent for stimulating open complex formation, suggesting that this DNA supercoiling-dependent component of Fis-mediated activation occurs in the absence of specific protein interactions between Fis and RNA polymerase. Fis-mediated translocation of superhelical energy from upstream binding sites to the promoter region may be a general feature of Fis-mediated activation of transcription at stable RNA promoters, which often contain A+T-rich upstream sequences.

摘要

大肠杆菌的leuV操纵子编码四种亮氨酰tRNA同工受体中的三种基因。已知来自该启动子及其他稳定RNA启动子的转录受顺式作用的上游元件以及Fis蛋白与RNA聚合酶α亚基羧基末端结构域相互作用的影响。在本报告中,我们提出leuV启动子的转录也由一种Fis介导的、依赖DNA超螺旋的机制激活,该机制类似于先前描述的ilvP(G)启动子的整合宿主因子(IHF)介导的机制(S.D.谢里丹等人,1998年,《生物化学杂志》273:21298 - 21308)。我们提供的证据表明,Fis结合导致超螺旋能量从超螺旋诱导的DNA双链不稳定(SIDD)区域的启动子远端部分转移到leuV启动子的启动子近端部分,该部分在开放复合物中解旋。一种与RNA聚合酶α亚基羧基末端结构域接触存在缺陷的突变Fis蛋白,仍有能力刺激开放复合物的形成,这表明Fis介导的激活中这种依赖DNA超螺旋的成分在没有Fis与RNA聚合酶之间特定蛋白相互作用的情况下也会发生。Fis介导的超螺旋能量从上游结合位点向启动子区域的转移可能是Fis介导稳定RNA启动子转录激活的一个普遍特征,这些启动子通常含有富含A + T的上游序列。

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