Department of Biology, University of Utah, Salt Lake City, UT 84112, USA.
Mol Microbiol. 2010 Mar;75(5):1272-84. doi: 10.1111/j.1365-2958.2010.07050.x. Epub 2010 Feb 1.
A molecular ruler, FliK, controls the length of the flagellar hook. FliK measures hook length and catalyses the secretion-substrate specificity switch from rod-hook substrate specificity to late substrate secretion, which includes the filament subunits. Here, we show normal hook-length control and filament assembly in the complete absence of the C-ring thus refuting the previous 'cup' model for hook-length control. Mutants of C-ring components, which are reported to produce short hooks, show a reduced rate of hook-basal body assembly thereby allowing for a premature secretion-substrate specificity switch. Unlike fliK null mutants, hook-length control in an autocleavage-defective mutant of flhB, the protein responsible for the switch to late substrate secretion, is completely abolished. FliK deletion variants that retain the ability to measure hook length are secreted thus demonstrating that FliK directly measures rod-hook length during the secretion process. Finally, we present a unifying model accounting for all published data on hook-length control in which FliK acts as a molecular ruler that takes measurements of rod-hook length while being intermittently secreted during the assembly process of the hook-basal body complex.
一个分子标尺 FliK 控制着鞭毛钩的长度。FliK 测量钩的长度并催化分泌底物特异性从杆钩底物特异性转变为晚期底物分泌,其中包括丝状体亚基。在这里,我们展示了在完全缺乏 C 环的情况下正常的钩长控制和丝状体组装,从而反驳了先前的钩长控制“杯”模型。据报道,C 环成分的突变体产生短钩,显示出较低的钩基底体组装速率,从而允许过早的分泌底物特异性转换。与 fliK 缺失突变体不同,flhB 的自身切割缺陷突变体(负责向晚期底物分泌的转换的蛋白质)中的钩长控制完全被废除。保留测量钩长能力的 fliK 缺失变体被分泌,因此证明 FliK 在分泌过程中直接测量杆钩长度。最后,我们提出了一个统一的模型,解释了所有关于钩长控制的已发表数据,其中 FliK 作为一个分子标尺,在钩基底体复合物的组装过程中,间歇地分泌并测量杆钩的长度。