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首页> 外文期刊>Molecular Microbiology >A partner‐switching regulatory system controls hormogonium development in the filamentous cyanobacterium Nostoc punctiforme Nostoc punctiforme
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A partner‐switching regulatory system controls hormogonium development in the filamentous cyanobacterium Nostoc punctiforme Nostoc punctiforme

机译:伴侣切换监管系统控制丝状蓝杆菌骨髓骨髓骨髓骨头骨头状骨折的霍莫昔米开发

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摘要

Summary Filamentous cyanobacteria exhibit developmental complexity, including the transient differentiation of motile hormogonia in many species. Using a forward genetic approach, a trio of genes unique to filamentous cyanobacteria encoding a putative Rsb‐like partner‐switching regulatory system (PSRS) was implicated in regulating hormogonium development in the model filamentous cyanobacterium Nostoc punctiforme . Analysis of in‐frame deletion strains indicated that HmpU (putative serine phosphatase) and HmpV (STAS domain) enhance, while HmpW (putative serine kinase) represses motility and persistence of the hormogonium state. Protein–protein interaction studies demonstrated specificity between HmpW and HmpV. Epistasis analysis between hmpW and hmpV was consistent with HmpV acting as the downstream effector of the system, rather than regulation of a sigma factor by HmpW. Deletion of hmpU or hmpV reduced accumulation of extracellular PilA and hormogonium polysaccharide (HPS), and expression of type IV pilus‐ and HPS‐specific genes was reduced in the Δ hmpV strain. Expression of the Hmp PSRS is induced in hormogonia, and the cytoplasmic localization of HmpV‐GFPuv implies that its downstream target is probably cytoplasmic as well. Collectively, these results support a model where HmpU and HmpW antagonistically regulate the phosphorylation state of HmpV, and subsequently, unphosphorylated HmpV positively regulates an undefined downstream target to affect hormogonium‐specific gene expression.
机译:发明内容丝状蓝杆菌表现出发育复杂性,包括许多物种中运动激素的瞬态分化。使用前进遗传方法,对编码推定的RSB的伴侣切换调节系统(PSRS)的丝状蓝细菌具有独特的基因是牵连在模型丝状蓝杆菌Nostock Puncteriforme中的嗅觉发育。框架内缺失菌株的分析表明,HMPU(推定丝氨酸磷酸酶)和HMPV(STAS结构域)增强,而HMPW(推定丝氨酸激酶)抑制了嗅觉状态的动力和持续性。蛋白质 - 蛋白质相互作用研究表明HMPW和HMPV之间的特异性。 HMPW和HMPV之间的简化分析与作为系统下游效应器的HMPV一致,而不是通过HMPW调节Sigma因子。缺失HMPU或HMPV减少细胞外皮和环核多糖(HPS)的积累,并且在δHMPV菌株中降低了IV型菌毛和HPS特异性基因的表达。 HMP PSRS的表达在Hormogonia中诱导,HMPV-GFPUV的细胞质定位意味着其下游靶也可能是细胞质。总的来说,这些结果支持HMPU和HMPW拮抗HMPV的磷酸化状态的模型,随后,不磷酸化的HMPV阳性调节未定义的下游靶以影响血型内核特异性基因表达。

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