首页> 美国卫生研究院文献>Journal of Bacteriology >The RNA Chaperone Hfq Independently Coordinates Expression of the VirB Type IV Secretion System and the LuxR-Type Regulator BabR in Brucella abortus 2308
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The RNA Chaperone Hfq Independently Coordinates Expression of the VirB Type IV Secretion System and the LuxR-Type Regulator BabR in Brucella abortus 2308

机译:RNA伴侣Hfq独立地协调流产布鲁氏菌2308中的VirB IV型分泌系统和LuxR型调节剂BabR的表达。

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摘要

The type IV secretion system encoded by the virB operon is required for full virulence of Brucella sp., and the present study links the RNA chaperone Hfq to wild-type expression of virB in Brucella abortus 2308. Studies employing virB-lacZ fusions, quantitative reverse transcription-PCR, and immunoblot analysis showed that both transcription and translation of virB are decreased in an isogenic hfq mutant compared to those in the parental strain. These results led to the hypothesis that Hfq regulation of virB is mediated through an intermediate transcriptional regulator. Subsequent experiments determined that expression of the gene encoding the putative Brucella quorum-sensing regulator BabR (also known as BlxR), a known virB regulator, is also controlled by Hfq at the posttranscriptional level, and a cis-acting element in the 5′ untranslated region of the babR transcript responsible for this regulation was identified. Consistent with its role as a virB regulator, recombinant Brucella BabR binds to the virB promoter region in electrophoretic mobility shift assays. However, experiments employing a babR mutant strain determined that BabR is a repressor, not an activator, of virB transcription. These findings suggest that Hfq regulates virB expression through both BabR-dependent and BabR-independent pathways.
机译:完全毒力的布鲁氏菌属需要由virB操纵子编码的IV型分泌系统,并且本研究将RNA伴侣Hfq与流产布鲁氏菌2308中的virB野生型表达联系起来。采用virB-lacZ融合的研究,定量反向转录PCR和免疫印迹分析表明,与亲本菌株相比,同基因hfq突变体中virB的转录和翻译均降低。这些结果导致了一个假设,即virB的Hfq调节是通过中间转录调节子介导的。随后的实验确定了编码假定的布鲁氏菌群体感应调节剂BabR(也称为BlxR)(一种已知的virB调节剂)的基因在转录后水平上也受到Hfq的控制,而5'端的顺式作用元件未翻译确定了负责该调控的babR转录本区域。与它作为virB调节剂的作用一致,重组布鲁氏菌BabR在电泳迁移率变动分析中与virB启动子区域结合。但是,使用 babR 突变株进行的实验确定BabR是virB 转录的阻遏物,而不是激活物。这些发现表明,Hfq通过BabR依赖性和BabR依赖性途径调节 virB 表达。

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