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In Silico Identification and Experimental Characterization of Regulatory Elements Controlling the Expression of the SalmonellacsrB and csrC Genes

机译:计算机控制沙门氏菌表达的调控元件的计算机鉴定和实验表征csrB和csrC基因

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摘要

The small RNAs CsrB and CsrC of Salmonella indirectly control the expression of numerous genes encoding widespread cellular functions, including virulence. The expression of csrB and csrC genes, which are located in different chromosomal regions, is coordinated by positive transcriptional control mediated by the two-component regulatory system BarA/SirA. Here, we identified by computational analysis an 18-bp inverted repeat (IR) sequence located far upstream from the promoter of Salmonella enterica serovar Typhimurium csrB and csrC genes. Deletion analysis and site-directed mutagenesis of the csrB and csrC regulatory regions revealed that this IR sequence is required for transcriptional activation of both genes. Protein-DNA and protein-protein interaction assays showed that the response regulator SirA specifically binds to the IR sequence and provide evidence that SirA acts as a dimer. Interestingly, whereas the IR sequence was essential for the SirA-mediated expression of csrB, our results revealed that SirA controls the expression of csrC not only by binding to the IR sequence but also by an indirect mode involving the Csr system. Additional computational, biochemical, and genetic analyses demonstrated that the integration host factor (IHF) global regulator positively controls the expression of csrB, but not of csrC, by interacting with a sequence located between the promoter and the SirA-binding site. These findings contribute to the better understanding of the regulatory mechanism controlling the expression of CsrB and CsrC.
机译:沙门氏菌的小RNA CsrB和CsrC间接控制众多编码广泛细胞功能(包括毒性)的基因的表达。位于两个不同染色体区域的csrB和csrC基因的表达,是由两组分调节系统BarA / SirA介导的阳性转录控制所协调的。在这里,我们通过计算分析确定了一个18 bp的反向重复(IR)序列,该序列位于肠炎沙门氏菌血清鼠伤寒杆菌csrB和csrC基因启动子的上游。 csrB和csrC调节区的缺失分析和定点诱变显示,这两个基因的转录激活都需要该IR序列。蛋白质-DNA和蛋白质-蛋白质相互作用分析表明,应答调节剂SirA与IR序列特异性结合,并提供证据表明SirA充当二聚体。有趣的是,尽管IR序列对于SirA介导的csrB表达是必不可少的,但我们的结果表明SirA不仅通过结合IR序列而且通过涉及Csr系统的间接模式来控制csrC的表达。其他的计算,生化和遗传分析表明,整合宿主因子(IHF)全局调节剂通过与启动子和SirA结合位点之间的序列相互作用,积极控制csrB的表达,而不控制csrC的表达。这些发现有助于更好地理解控制CsrB和CsrC表达的调节机制。

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