Mishra Meenu, Deora Rajendar
Department of Microbiology and Immunology, Wake Forest University Health Sciences, Medical Center Blvd., Gray 5086, Winston-Salem, North Carolina 27157, USA.
J Bacteriol. 2005 Sep;187(18):6290-9. doi: 10.1128/JB.187.18.6290-6299.2005.
The Bordetella BvgAS signal transduction system controls the transition among at least three known phenotypic phases (Bvg+, Bvg(i), 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 Bvg(i) 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.
博德特氏菌BvgAS信号转导系统控制至少三种已知表型阶段(Bvg +、Bvg(i)和Bvg -)之间的转变以及许多具有不同阶段特异性表达谱的基因的表达。沿着Bvg信号连续体对基因表达的这种复杂调控,以bipA基因最为典型,该基因在Bvg +阶段低水平表达,在Bvg(i)阶段高水平表达,而在Bvg -阶段检测不到表达。bipA启动子有多个BvgA结合位点,它们发挥着不同的调控作用。我们之前推测,bipA的表达谱是由于细胞内磷酸化BvgA(BvgA-P)水平变化导致各种BvgA结合位点占据情况不同的结果。在本报告中,我们为该模型提供了体外证据,并表明bipA表达在低浓度BvgA-P时被激活,在高浓度时被抑制。通过使用独立的DNA结合试验,我们证明在激活条件下,BvgA与RNA聚合酶(RNAP)的结合存在协同效应,导致在启动子处形成开放复合物。我们进一步表明,在体外条件下,当bipA转录最小时,RNAP与BvgA-P对bipA启动子的结合存在竞争。我们的结果表明,BvgA结合位点IR2在介导这种抑制中起核心作用。