首页> 外文期刊>Journal of bacteriology >Regulation of the Response Regulator Gene degU through the Binding of SinR/SlrR and Exclusion of SinR/SlrR by DegU in Bacillus subtilis
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Regulation of the Response Regulator Gene degU through the Binding of SinR/SlrR and Exclusion of SinR/SlrR by DegU in Bacillus subtilis

机译:通过SinR / SlrR的结合和DegU排除枯草芽孢杆菌对SinR / SlrR的反应,调节反应基因degU。

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Bacillus subtilis DegU is a response regulator of the DegS-DegU two-component regulatory system. Phosphorylated DegU (DegU-P) controls many genes and biological processes, such as exoprotease and γ-polyglutamic acid production, in addition to the degU gene, by binding to target gene promoters. Nonphosphorylated DegU and low levels of DegU-P are required for swarming motility and genetic competence. The DNA-binding repressors SinR and SlrR are part of a double-negative feedback loop and comprise the epigenetic switch governing biofilm formation. In this study, we found that SinR repressed degU. Furthermore, SlrR, which interacts with SinR through protein-protein interaction, seems to have an active role in degU expression in in vivo lacZ analysis. An in vitro transcription assay supported this observation. An electrophoretic mobility shift assay (EMSA) showed that SinR bound to the degU promoter and that SlrR formed a complex with SinR on the degU promoter. In EMSA, DegU-P excluded the SinR/SlrR complex but not SinR from the degU promoter in the presence of RNA polymerase. These findings suggest that DegU-P interacts with SlrR. In support of this hypothesis, disruption of the slrR gene resulted in decreased degU expression. This newly identified regulatory mechanism for degU is considered to be sequential transcription factor replacement.
机译:枯草芽孢杆菌DegU是DegS-DegU两组分调节系统的响应调节剂。磷酸化的DegU(DegU-P)通过结合靶基因启动子来控制许多基因和生物学过程,例如除exemU 基因外的蛋白酶和γ-聚谷氨酸的生产。群体运动和遗传能力需要非磷酸化的DegU和低水平的DegU-P。 DNA结合阻遏物SinR和SlrR是双负反馈环的一部分,并包含控制生物膜形成的表观遗传开关。在这项研究中,我们发现SinR抑制了 degU 。此外,通过蛋白-蛋白相互作用与SinR相互作用的SlrR在体内lacZ 分析中似乎在 degU 表达中起积极作用。一项体外转录试验支持了这一观察结果。电泳迁移率迁移分析(EMSA)表明,SinR与 degU 启动子结合,而SrrR与 degU 启动子上的SinR形成复合物。在EMSA中,在存在RNA聚合酶的情况下,DegU-P从 degU 启动子中排除了SinR / SlrR复合物,但不排除SinR。这些发现表明DegU-P与SlrR相互作用。支持该假设的是, slrR 基因的破坏导致 degU 表达的降低。新发现的 degU 调控机制被认为是顺序转录因子的替代。

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