Yu J, Shapiro L
Department of Developmental Biology, Beckman Center, Stanford University School of Medicine, California 94305-5427.
J Bacteriol. 1992 May;174(10):3327-38. doi: 10.1128/jb.174.10.3327-3338.1992.
The biogenesis of the Caulobacter crescentus polar flagellum requires the expression of more than 48 genes, which are organized in a regulatory hierarchy. The flbO locus is near the top of the hierarchy, and consequently strains with mutations in this locus are nonmotile and lack the flagellar basal body complex. In addition to the motility phenotype, mutations in this locus also cause abnormal cell division. Complementing clones restore both motility and normal cell division. Sequence analysis of a complementing subclone revealed that this locus encodes at least two proteins that are homologs of the Salmonella typhimurium and Escherichia coli flagellar proteins FliL and FliM. FliM is thought to be a switch protein and to interface with the flagellum motor. The C. crescentus fliL and fliM genes form an operon that is expressed early in the cell cycle. Tn5 insertions in the fliM gene prevent the transcription of class II and class III flagellar genes, which are lower in the regulatory hierarchy. The start site of the fliLM operon lies 166 bp from the divergently transcribed flaCBD operon that encodes several basal body genes. Sequence comparison of the fliL transcription start site with those of other class I genes, flaS and flaO, revealed a highly conserved 29-bp sequence in a potential promoter region that differs from sigma 70, sigma 54, sigma 32, and sigma 28 promoter sequences, suggesting that at least three class I genes share a unique 5' regulatory region.
新月柄杆菌极性鞭毛的生物合成需要48个以上基因的表达,这些基因按调控层次组织。flbO基因座接近该层次结构的顶部,因此该基因座发生突变的菌株无运动能力,且缺乏鞭毛基体复合体。除了运动表型外,该基因座的突变还会导致异常细胞分裂。互补克隆可恢复运动能力和正常细胞分裂。对一个互补亚克隆的序列分析表明,该基因座编码至少两种与鼠伤寒沙门氏菌和大肠杆菌鞭毛蛋白FliL和FliM同源的蛋白质。FliM被认为是一种开关蛋白,并与鞭毛马达相互作用。新月柄杆菌fliL和fliM基因形成一个操纵子,在细胞周期早期表达。fliM基因中的Tn5插入阻止了调控层次较低的II类和III类鞭毛基因的转录。fliLM操纵子的起始位点距离编码几个基体基因的反向转录的flaCBD操纵子166 bp。fliL转录起始位点与其他I类基因flaS和flaO的转录起始位点的序列比较显示,在一个潜在启动子区域存在一个高度保守的29 bp序列,该序列不同于sigma 70、sigma 54、sigma 32和sigma 28启动子序列,这表明至少三个I类基因共享一个独特的5'调控区域。