首页> 美国卫生研究院文献>Journal of Bacteriology >Mode of Action of the Bordetella BvgA Protein: Transcriptional Activation and Repression of the Bordetella bronchiseptica bipA Promoter
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Mode of Action of the Bordetella BvgA Protein: Transcriptional Activation and Repression of the Bordetella bronchiseptica bipA Promoter

机译:博德特氏菌BvgA蛋白的作用模式:支气管败血性博德特氏菌bipA启动子的转录激活和抑制。

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摘要

The Bordetella BvgAS signal transduction system controls the transition among at least three known phenotypic phases (Bvg+, Bvgi, and Bvg) and the expression of a number of genes which have distinct phase-specific expression profiles. This complex regulation of gene expression along the Bvg signaling continuum is best exemplified by the gene bipA, which is expressed at a low level in the Bvg+ phase, at a maximal level in the Bvgi phase, and at undetectable levels in the Bvg phase. The bipA promoter has multiple BvgA binding sites which play distinct regulatory roles. We had previously speculated that the expression profile of bipA is a consequence of the differential occupancy of the various BvgA binding sites as a result of variation in the levels of phosphorylated BvgA (BvgA-P) inside the cell. In this report, we provide in vitro evidence for this model and show that bipA expression is activated at low concentrations of BvgA-P and is repressed at high concentrations. By using independent DNA binding assays, we demonstrate that under activating conditions there is a synergistic effect on the binding of BvgA and RNA polymerase (RNAP), leading to the formation of open complexes at the promoter. We further show that, under in vitro conditions, when bipA transcription is minimal, there is competition between the binding of RNAP and BvgA-P to the bipA promoter. Our results show that the BvgA binding site IR2 plays a central role in mediating this repression.
机译:博德特氏菌BvgAS信号转导系统控制至少三个已知表型阶段(Bvg + ,Bvg i 和Bvg -)之间的过渡。具有不同阶段特异性表达谱的许多基因的表达。沿Bvg信号连续体对基因表达的这种复杂调节最好用bibA基因来例证,该基因在Bvg + 阶段以低水平表达,而在Bvg i处于最高水平。 阶段,在Bvg -阶段处于不可检测的水平。 bipA启动子具有多个BvgA结合位点,这些位点起着独特的调节作用。我们先前曾推测,由于细胞内磷酸化BvgA(BvgA-P)水平的变化,bipA的表达谱是各种BvgA结合位点差异性占据的结果。在本报告中,我们提供了该模型的体外证据,并显示bipA表达在低浓度的BvgA-P时被激活,而在高浓度时被抑制。通过使用独立的DNA结合测定,我们证明了在激活条件下BvgA和RNA聚合酶(RNAP)的结合具有协同作用,导致在启动子上形成开放复合物。我们进一步表明,在体外条件下,当bipA转录极少时,RNAP和BvgA-P与bipA启动子的结合之间存在竞争。我们的结果表明,BvgA结合位点IR2在介导这种抑制中起着核心作用。

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