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BadR(BB0693)通过识别TAAAATAT基序来控制伯氏疏螺旋体中rpoS和bosR的生长阶段依赖性诱导。

BadR (BB0693) controls growth phase-dependent induction of rpoS and bosR in Borrelia burgdorferi via recognizing TAAAATAT motifs.

作者信息

Ouyang Zhiming, Zhou Jianli

机构信息

Department of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.

出版信息

Mol Microbiol. 2015 Dec;98(6):1147-67. doi: 10.1111/mmi.13206. Epub 2015 Sep 25.

Abstract

In Borrelia burgdorferi (Bb), the alternative sigma factor RpoS plays a central role during Bb's adaptation to ticks and mammals. Previous studies have demonstrated that RpoS is not expressed during the early stages of spirochetal growth or when Bb resides in ticks during the intermolt phase, but the molecular details of these events remain unknown. In the current study, biomagnetic bead separation of rpoS promoter-binding proteins, coupled with genetic inactivation, was employed to identify BadR (BB0693) as a negative regulator that controls growth phase-dependent induction of rpoS and bosR in Bb. When badR was inactivated, the expression of rpoS and bosR was induced only during the early stages of bacterial growth, but not during the stationary growth phase. Recombinant BadR bound to the promoter DNA of rpoS and the regulatory region upstream of bosR via AT-rich TAAAATAT motifs. Mutations in this motif markedly inhibited or abolished rBadR binding. These results suggest that BadR directly influences the expression of both rpoS and bosR in Bb. This newly recognized role for BadR to fine-tune the activation of the RpoN-RpoS pathway at strategic times in Bb's life cycle potentially represents another layer of gene control over σ(54)-dependent gene regulation.

摘要

在伯氏疏螺旋体(Bb)中,替代西格玛因子RpoS在Bb适应蜱虫和哺乳动物的过程中起着核心作用。先前的研究表明,在螺旋体生长的早期阶段或Bb在蜱虫的蜕皮间期时,RpoS不表达,但这些事件的分子细节仍然未知。在当前的研究中,利用生物磁珠分离rpoS启动子结合蛋白,并结合基因失活,来鉴定BadR(BB0693)作为一种负调控因子,它控制Bb中rpoS和bosR的生长阶段依赖性诱导。当badR失活时,rpoS和bosR的表达仅在细菌生长的早期阶段被诱导,而在稳定生长阶段则不被诱导。重组BadR通过富含AT的TAAAATAT基序与rpoS的启动子DNA和bosR上游的调控区域结合。该基序中的突变显著抑制或消除了rBadR的结合。这些结果表明,BadR直接影响Bb中rpoS和bosR的表达。BadR在Bb生命周期的关键时期对RpoN-RpoS途径的激活进行微调的这一新发现的作用,可能代表了对σ(54)依赖性基因调控的另一层基因控制。

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