Anderson D K, Newton A
Department of Molecular Biology, Princeton University, New Jersey 08544, USA.
J Bacteriol. 1997 Apr;179(7):2281-8. doi: 10.1128/jb.179.7.2281-2288.1997.
Flagellum formation in Caulobacter crescentus requires ca. 50 flagellar genes, most of which belong to one of three classes (II, III, or IV). Epistasis experiments suggest that flagellar gene expression is coordinated with flagellum biosynthesis by two assembly checkpoints. Completion of the M/S ring-switch complex is required for the transition from class II to class III gene expression, and completion of the basal body-hook structure is required for the transition from class III to class IV gene expression. In studies focused on regulation of the class IV flagellin genes, we have examined fljK and fljL expression in a large number of flagellar mutants by using transcription and translation fusions to lacZ, nuclease S1 assays, and measurements of protein stability. The fljK-lacZ and fljL-lacZ transcription fusions were expressed in all class III flagellar mutants, although these strains do not make detectable 25- or 27-kDa flagellins. The finding that the fljK-lacZ translation fusion was not expressed in the same collection of class III mutants confirmed that fljK is regulated posttranscriptionally. The requirement of multiple class III genes for expression of the fljK-lacZ fusion suggests that completion of the basal body-hook is an assembly checkpoint for the posttranscriptional regulation of this flagellin gene. Deletion analysis within the 5' untranslated region of fljK identified a sequence between +24 and +38 required for regulation of the fljK-lacZ fusion by class III genes, which implicates an imperfect 14-bp direct repeat in the posttranscriptional regulation of fljK. Our results show that fljL is also regulated posttranscriptionally by class III and unclassified flagellar genes, apparently by a mechanism different from the one regulating fljK.
新月柄杆菌鞭毛的形成需要约50个鞭毛基因,其中大部分属于三个类别(II、III或IV)之一。上位性实验表明,鞭毛基因表达通过两个组装检查点与鞭毛生物合成相协调。从II类基因表达转变为III类基因表达需要M/S环开关复合体的完成,而从III类基因表达转变为IV类基因表达则需要基体-钩结构的完成。在聚焦于IV类鞭毛蛋白基因调控的研究中,我们通过使用与lacZ的转录和翻译融合、核酸酶S1分析以及蛋白质稳定性测量,检测了大量鞭毛突变体中fljK和fljL的表达。fljK-lacZ和fljL-lacZ转录融合在所有III类鞭毛突变体中均有表达,尽管这些菌株无法产生可检测到的25 kDa或27 kDa鞭毛蛋白。fljK-lacZ翻译融合在同一组III类突变体中未表达,这一发现证实fljK在转录后受到调控。fljK-lacZ融合表达需要多个III类基因,这表明基体-钩的完成是该鞭毛蛋白基因转录后调控的一个组装检查点。对fljK 5'非翻译区内的缺失分析确定了+24至+38之间的一个序列,该序列是III类基因对fljK-lacZ融合进行调控所必需的,这表明在fljK的转录后调控中存在一个不完美的14 bp直接重复序列。我们的结果表明,fljL在转录后也受到III类和未分类的鞭毛基因调控,其调控机制显然与调控fljK的机制不同。