Mangan E K, Malakooti J, Caballero A, Anderson P, Ely B, Gober J W
Department of Chemistry and Biochemistry and Molecular Biology Institute, University of California-Los Angeles, Los Angeles, California 90095-1569, USA.
J Bacteriol. 1999 Oct;181(19):6160-70. doi: 10.1128/JB.181.19.6160-6170.1999.
The biogenesis of the polar flagellum of Caulobacter crescentus is regulated by the cell cycle as well as by a trans-acting regulatory hierarchy that functions to couple flagellum assembly to gene expression. The assembly of early flagellar structures (MS ring, switch, and flagellum-specific secretory system) is required for the transcription of class III genes, which encode the remainder of the basal body and the external hook structure. Similarly, the assembly of class III gene-encoded structures is required for the expression of the class IV flagellins, which are incorporated into the flagellar filament. Here, we demonstrate that mutations in flbT, a flagellar gene of unknown function, can restore flagellin protein synthesis and the expression of fljK::lacZ (25-kDa flagellin) protein fusions in class III flagellar mutants. These results suggest that FlbT functions to negatively regulate flagellin expression in the absence of flagellum assembly. Deletion analysis shows that sequences within the 5' untranslated region of the fljK transcript are sufficient for FlbT regulation. To determine the mechanism of FlbT-mediated regulation, we assayed the stability of fljK mRNA. The half-life (t(1/2)) of fljK mRNA in wild-type cells was approximately 11 min and was reduced to less than 1.5 min in a flgE (hook) mutant. A flgE flbT double mutant exhibited an mRNA t(1/2) of greater than 30 min. This suggests that the primary effect of FlbT regulation is an increased turnover of flagellin mRNA. The increased t(1/2) of fljK mRNA in a flbT mutant has consequences for the temporal expression of fljK. In contrast to the case for wild-type cells, fljK::lacZ protein fusions in the mutant are expressed almost continuously throughout the C. crescentus cell cycle, suggesting that coupling of flagellin gene expression to assembly has a critical influence on regulating cell cycle expression.
新月柄杆菌极鞭毛的生物合成受细胞周期以及一个反式作用调控层级的调节,该调控层级的作用是将鞭毛组装与基因表达联系起来。III类基因的转录需要早期鞭毛结构(MS环、开关和鞭毛特异性分泌系统)的组装,这些基因编码基体的其余部分和外部钩状结构。同样,IV类鞭毛蛋白的表达需要III类基因编码结构的组装,这些鞭毛蛋白会被整合到鞭毛丝中。在这里,我们证明,flbT(一个功能未知的鞭毛基因)中的突变可以恢复III类鞭毛突变体中鞭毛蛋白的合成以及fljK::lacZ(25 kDa鞭毛蛋白)蛋白融合体的表达。这些结果表明,在没有鞭毛组装的情况下,FlbT的功能是负向调节鞭毛蛋白的表达。缺失分析表明,fljK转录本5'非翻译区内的序列足以进行FlbT调节。为了确定FlbT介导的调节机制,我们检测了fljK mRNA的稳定性。野生型细胞中fljK mRNA的半衰期(t(1/2))约为11分钟,在flgE(钩状结构)突变体中降至不到分钟。flgE flbT双突变体的mRNA t(1/2)大于30分钟。这表明FlbT调节的主要作用是增加鞭毛蛋白mRNA的周转。flbT突变体中fljK mRNA t(1/2)的增加对fljK的时间表达有影响。与野生型细胞不同,突变体中的fljK::lacZ蛋白融合体在新月柄杆菌的整个细胞周期中几乎持续表达,这表明鞭毛蛋白基因表达与组装的耦合对调节细胞周期表达有至关重要的影响。