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恶臭假单胞菌鞭毛系统的转录组织与调控

Transcriptional organization and regulation of the Pseudomonas putida flagellar system.

作者信息

Leal-Morales Antonio, Pulido-Sánchez Marta, López-Sánchez Aroa, Govantes Fernando

机构信息

Centro Andaluz de Biología del Desarrollo, Universidad Pablo de Olavide/Consejo Superior de Investigaciones Científicas/Junta de Andalucía and Departamento de Biología Molecular e Ingeniería Bioquímica, Universidad Pablo de Olavide, Sevilla, Spain.

出版信息

Environ Microbiol. 2022 Jan;24(1):137-157. doi: 10.1111/1462-2920.15857. Epub 2021 Dec 2.

Abstract

A single region of the Pseudomonas putida genome, designated the flagellar cluster, includes 59 genes potentially involved in the biogenesis and function of the flagellar system. Here, we combine bioinformatics and in vivo gene expression analyses to clarify the transcriptional organization and regulation of the flagellar genes in the cluster. We have identified 11 flagellar operons and characterized 22 primary and internal promoter regions. Our results indicate that synthesis of the flagellar apparatus and core chemotaxis machinery is regulated by a three-tier cascade in which fleQ is a Class I gene, standing at the top of the transcriptional hierarchy. FleQ- and σ -dependent Class II genes encode most components of the flagellar structure, part of the chemotaxis machinery and multiple regulatory elements, including the flagellar σ factor FliA. FliA activation of Class III genes enables synthesis of the filament, one stator complex and completion of the chemotaxis apparatus. Accessory regulatory proteins and an intricate operon architecture add complexity to the regulation by providing feedback and feed-forward loops to the main circuit. Because of the high conservation of the gene arrangement and promoter motifs, we believe that the regulatory circuit presented here may also apply to other environmental pseudomonads.

摘要

恶臭假单胞菌基因组的一个单一区域,称为鞭毛簇,包含59个可能参与鞭毛系统生物合成和功能的基因。在这里,我们结合生物信息学和体内基因表达分析,以阐明该簇中鞭毛基因的转录组织和调控。我们已经鉴定出11个鞭毛操纵子,并对22个主要和内部启动子区域进行了表征。我们的结果表明,鞭毛装置和核心趋化机制的合成受三级级联调控,其中fleQ是I类基因,处于转录层次结构的顶端。FleQ和σ依赖性II类基因编码鞭毛结构的大部分组件、趋化机制的一部分以及多个调控元件,包括鞭毛σ因子FliA。III类基因的FliA激活能够合成鞭毛丝、一个定子复合体并完成趋化装置。辅助调控蛋白和复杂的操纵子结构通过向主回路提供反馈和前馈环增加了调控的复杂性。由于基因排列和启动子基序的高度保守性,我们认为这里提出的调控回路也可能适用于其他环境假单胞菌。

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