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The Gac-Rsm and SadB Signal Transduction Pathways Converge on AlgU to Downregulate Motility in Pseudomonas fluorescens

机译:Gac-Rsm和SadB信号转导途径在AlgU上汇聚以下调荧光假单胞菌的运动性。

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摘要

Flagella mediated motility in Pseudomonas fluorescens F113 is tightly regulated. We have previously shown that motility is repressed by the GacA/GacS system and by SadB through downregulation of the fleQ gene, encoding the master regulator of the synthesis of flagellar components, including the flagellin FliC. Here we show that both regulatory pathways converge in the regulation of transcription and possibly translation of the algU gene, which encodes a sigma factor. AlgU is required for multiple functions, including the expression of the amrZ gene which encodes a transcriptional repressor of fleQ. Gac regulation of algU occurs during exponential growth and is exerted through the RNA binding proteins RsmA and RsmE but not RsmI. RNA immunoprecipitation assays have shown that the RsmA protein binds to a polycistronic mRNA encoding algU, mucA, mucB and mucD, resulting in lower levels of algU. We propose a model for repression of the synthesis of the flagellar apparatus linking extracellular and intracellular signalling with the levels of AlgU and a new physiological role for the Gac system in the downregulation of flagella biosynthesis during exponential growth.
机译:鞭毛介导的荧光假单胞菌F113的运动受到严格调节。我们以前已经表明,通过下调fleQ基因(编码鞭毛成分包括鞭毛蛋白FliC的主调节剂),GacA / GacS系统和SadB抑制了运动性。在这里,我们显示两种调节途径均会收敛于编码sigma因子的algU基因的转录和可能的翻译调控。 AlgU是多种功能所必需的,包括编码fleQ转录阻遏物的amrZ基因的表达。对algU的Gac调节发生在指数增长期间,并通过RNA结合蛋白RsmA和RsmE发挥作用,而不是通过RsmI发挥作用。 RNA免疫沉淀试验表明,RsmA蛋白与编码algU,mucA,mucB和mucD的多顺反子mRNA结合,导致algU含量降低。我们提出了一种抑制鞭毛装置合成的模型,该鞭毛装置将细胞外和细胞内信号传导与AlgU的水平联系起来,并且在指数生长过程中鞭毛生物合成的下调中Gac系统的新生理作用。

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