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首页> 外文期刊>Microbiology >Phosphate starvation relayed by PhoB activates the expression of the Pseudomonas aeruginosa σvreI ECF factor and its target genes
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Phosphate starvation relayed by PhoB activates the expression of the Pseudomonas aeruginosa σvreI ECF factor and its target genes

机译:PhoB传递的磷酸饥饿会激活铜绿假单胞菌σvreIECF因子及其靶基因的表达

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The cell-surface signalling (CSS) system represents an important regulatory mechanism by which Gram-negative bacteria respond to the environment. Gene regulation by CSS systems is particularly present and important in the opportunistic human pathogen Pseudomonas aeruginosa. In this bacterium, these mechanisms regulate mainly the uptake of iron, but also virulence functions. The latter is the case for the P. aeruginosa PUMA3 CSS system formed by the putative VreA receptor, the σVreI extracytoplasmic function sigma factor and the VreR anti-sigma factor. A role for this system in P. aeruginosa virulence has been demonstrated previously. However, the conditions under which this system is expressed and activated have not been elucidated so far. In this work, we have identified and characterized the global regulatory cascade activating the expression of the PUMA3 system. We show that the PhoB transcriptional regulator, part of the PhoB-PhoR two-component signalling system, can sense a limitation of inorganic phosphate to turn on the expression of the vreA, vreI and vreR genes, which constitute an operon. Upon expression of these genes in this condition, σVreI factor mediates transcription of most, but not all, of the previously identified σVreI-regulated genes. Indeed, we found new σVreI-targeted genes and we show that σVreI-regulon genes are all located immediately downstream to the vreAIR gene cluster.
机译:细胞表面信号(CSS)系统代表了革兰氏阴性细菌对环境做出反应的重要调控机制。 CSS系统对基因的调控在机会性人类病原体铜绿假单胞菌中尤为重要。在这种细菌中,这些机制主要调节铁的吸收,但也调节毒力功能。后者是由假定的VreA受体,σVreI胞外功能sigma因子和VreR抗sigma因子组成的铜绿假单胞菌PUMA3 CSS系统的情况。先前已经证明了该系统在铜绿假单胞菌毒力中的作用。但是,到目前为止尚未阐明表达和激活该系统的条件。在这项工作中,我们已经确定并表征了激活PUMA3系统表达的全局调节级联反应。我们表明,PhoB转录调节剂,PhoB-PhoR两组分信号系统的一部分,可以感觉到无机磷酸盐的局限性,从而开启了构成操纵子的vreA,vreI和vreR基因的表达。在这种条件下表达这些基因后,σVreI因子介导了大多数但不是全部先前鉴定的σVreI调控基因的转录。确实,我们发现了新的靶向σVreI的基因,并且我们证明σVreI调节基因均位于vreAIR基因簇的紧邻下游。

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