首页> 美国卫生研究院文献>Journal of Bacteriology >H-NS Antagonism in Shigella flexneri by VirB a Virulence Gene Transcription Regulator That Is Closely Related to Plasmid Partition Factors
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H-NS Antagonism in Shigella flexneri by VirB a Virulence Gene Transcription Regulator That Is Closely Related to Plasmid Partition Factors

机译:弗氏志贺氏菌的H-NS拮抗作用VirB是一种与质粒分配因子密切相关的毒力基因转录调节剂

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摘要

The VirB protein of Shigella flexneri is a positive regulator of the major virulence operons of this enteroinvasive intracellular pathogen. VirB resembles no other transcription factor but is strongly homologous to plasmid partition proteins. We found that the binding of the VirB protein to the promoter region of the icsB virulence gene induced hypersensitivity to cleavage by DNase I over a region to which the H-NS repressor protein binds and completely abolished the protection of this sequence from DNase I by H-NS. In the absence of H-NS, the VirB protein had no additive effect on the ability of the icsB promoter to form an open transcription complex, indicating that VirB is not involved in the recruitment of RNA polymerase to the promoter or in open complex formation. Similarly, VirB did not stimulate promoter function in an in vitro transcription assay but acted as an antagonist of H-NS-mediated repression. A sequence located upstream of the icsB promoter and related to cis-acting elements involved in plasmid partitioning was required for promoter derepression by VirB. Alterations to one heptameric motif within this DNA sequence attenuated VirB binding and derepression of icsB transcription.
机译:弗氏志贺氏菌的VirB蛋白是这种肠道侵袭性细胞内病原体主要毒力操纵子的正向调节剂。 VirB与其他转录因子相似,但与质粒分配蛋白高度同源。我们发现,VirB蛋白与icsB毒力基因启动子区域的结合诱导了H-NS阻遏蛋白结合区域上对DNase I切割的超敏反应,并完全废除了H对该序列的保护。 -NS。在没有H-NS的情况下,VirB蛋白对icsB启动子形成开放转录复合物的能力没有累加作用,表明VirB不参与RNA聚合酶向启动子的募集或开放复合物的形成。同样,VirB在体外转录测定中不刺激启动子功能,但可作为H-NS介导的阻抑的拮抗剂。通过VirB抑制启动子需要位于icsB启动子上游并与参与质粒分配的顺式作用元件相关的序列。该DNA序列中一个七聚体基序的改变减弱了VirB的结合并抑制了icsB转录。

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