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Pseudomonas syringae Two-Component Response Regulator RhpR Regulates Promoters Carrying an Inverted Repeat Element

机译:丁香假单胞菌两组分响应调节剂RhpR调节携带反向重复元件的启动子。

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The two-component system RhpRS was identified in Pseudomonas syringae as a regulator of the genes encoding the type III secretion system and type III effector proteins (together called the T3 genes). In the absence of the sensor kinase RhpS, the response regulator RhpR represses the induction of the T3 gene regulatory cascade consisting of hrpRS , hrpL , and the T3 genes in a phosphorylation-dependent manner. The repressor activity of RhpR is inhibited by RhpS, which presumably acts as a phosphatase under the T3 gene inducing conditions. Here, we show that RhpR binds and induces its own promoter in a phosphorylation-dependent manner. Deletion and mutagenesis analyses revealed an inverted repeat (IR) element, GTATC-N6-GATAC, in the rhpR promoter that confers the RhpR-dependent induction. Computational search of the P. syringae genomes for the putative IR elements and Northern blot analysis of the genes with a putative IR element in the promoter region uncovered five genes that were upregulated and two genes that were downregulated in an RhpR-dependent manner. Two genes that were strongly induced by RhpR were assayed for the IR element activity in gene regulation and, in both cases, the IR element mediated the RhpR-dependent gene induction. Chromatin immunoprecipitation assays indicated that RhpR binds the promoters containing a putative IR element but not the hrpR and hrpL promoters that do not have an IR element, suggesting that RhpR indirectly regulates the transcriptional cascade of hrpRS , hrpL , and the T3 genes.
机译:丁香假单胞菌中鉴定出一种由两部分组成的系统RhpRS作为编码III型分泌系统和III型效应蛋白(统称为T3基因)的基因的调节剂。在缺少传感器激酶RhpS的情况下,响应调节剂RhpR以磷酸化依赖性方式抑制由hrpRS,hrpL和T3基因组成的T3基因调节级联的诱导。 RhpS的阻遏物活性受到RhpS的抑制,RhpS可能在T3基因诱导条件下起磷酸酶的作用。在这里,我们显示RhpR结合并以磷酸化依赖性方式诱导其自身的启动子。缺失和诱变分析显示,rhpR启动子中的反向重复(IR)元件GTATC-N 6 -GATAC赋予了RhpR依赖性诱导作用。丁香假单胞菌基因组的计算搜索以寻找推定的IR元件,并在启动子区域中用推定的IR元件对基因进行Northern印迹分析,发现五个基因被上调,两个基因被RhpR-依赖性方式下调。分析了在基因调控中被RhpR强烈诱导的两个基因的IR元件活性,并且在两种情况下,IR元件都介导了RhpR依赖性基因诱导。染色质免疫沉淀试验表明,RhpR与含有推定的IR元件的启动子结合,但不与不具有IR元件的hrpR和hrpL启动子结合,这表明RhpR间接调节hrpRS,hrpL和T3基因的转录级联。

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