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新月柄杆菌中鞭毛近端杆编码基因的时间调控。

Temporal regulation of genes encoding the flagellar proximal rod in Caulobacter crescentus.

作者信息

Boyd C H, Gober J W

机构信息

Department of Chemistry and Biochemistry and the Molecular Biology Institute, University of California at Los Angeles, Los Angeles, California 90095-1569, USA.

出版信息

J Bacteriol. 2001 Jan;183(2):725-35. doi: 10.1128/JB.183.2.725-735.2001.

Abstract

The gram-negative bacterium Caulobacter crescentus has a life cycle that includes two distinct and separable developmental stages, a motile swarmer phase and a sessile stalked phase. The cell cycle-controlled biogenesis of the single polar flagellum of the swarmer cell is the best-studied aspect of this developmental program. The flagellar regulon is arranged into a rigid trans-acting hierarchy of gene expression in which successful expression of early genes is required for the expression of genes that are later in the hierarchy and in which the order of gene expression mirrors the order of assembly of gene products into the completed flagellum. The flgBC-fliE genes were identified as a result of the C. crescentus genome sequencing project and encode the homologues of two flagellar proximal rod proteins, FlgB and FlgC, and one conserved protein, FliE, that is of unknown function. Footprint assays on a DNA fragment containing the operon promoter as well as in vivo mutant suppressor analysis of promoter mutations indicate that this operon is controlled by the cell cycle response regulator CtrA, which with sigma(70) is responsible for regulating transcription of other early flagellar genes in C. crescentus. Promoter analysis, timing of expression, and epistasis experiments place these genes outside of the flagellar regulatory hierarchy; they are expressed in class II mutants, and flgB deletions do not prevent class III gene expression. This operon is also unusual in that it is expressed from a promoter that is divergent from the class II operon containing fliP, which encodes a member of the flagellum-specific protein export apparatus.

摘要

革兰氏阴性菌新月柄杆菌具有一个生命周期,其中包括两个不同且可分离的发育阶段,即游动的游泳体阶段和固着的柄细胞阶段。游泳体细胞单个极鞭毛的细胞周期控制生物合成是该发育程序中研究得最为透彻的方面。鞭毛调控子被安排成一个严格的基因表达反式作用层次结构,其中早期基因的成功表达是层次结构中较晚基因表达所必需的,并且基因表达的顺序反映了基因产物组装成完整鞭毛的顺序。flgBC - fliE基因是新月柄杆菌基因组测序项目的结果,编码两种鞭毛近端杆蛋白FlgB和FlgC的同源物,以及一种功能未知的保守蛋白FliE。对包含操纵子启动子的DNA片段进行足迹分析以及对启动子突变进行体内突变体抑制分析表明,该操纵子受细胞周期响应调节因子CtrA控制,CtrA与σ(70)一起负责调节新月柄杆菌中其他早期鞭毛基因的转录。启动子分析、表达时间和上位性实验将这些基因置于鞭毛调控层次结构之外;它们在II类突变体中表达,并且flgB缺失并不阻止III类基因的表达。该操纵子也很不寻常,因为它是从一个与包含fliP的II类操纵子不同向的启动子表达的,fliP编码鞭毛特异性蛋白输出装置的一个成员。

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