Ringgaard Simon, van Zon Jeroen, Howard Martin, Gerdes Kenn
Centre for Bacterial Cell Biology, Institute for Cell and Molecular Biosciences, Newcastle University, Newcastle upon Tyne NE2 4HH, United Kingdom.
Proc Natl Acad Sci U S A. 2009 Nov 17;106(46):19369-74. doi: 10.1073/pnas.0908347106. Epub 2009 Nov 11.
Bacterial plasmids encode partitioning (par) loci that confer stable plasmid inheritance. We showed previously that, in the presence of ParB and parC encoded by the par2 locus of plasmid pB171, ParA formed cytoskeletal-like structures that dynamically relocated over the nucleoid. Simultaneously, the par2 locus distributed plasmids regularly over the nucleoid. We show here that the dynamic ParA patterns are not simple oscillations. Rather, ParA nucleates and polymerizes in between plasmids. When a ParA assembly reaches a plasmid, the assembly reaction reverses into disassembly. Strikingly, plasmids consistently migrate behind disassembling ParA cytoskeletal structures, suggesting that ParA filaments pull plasmids by depolymerization. The perpetual cycles of ParA assembly and disassembly result in continuous relocation of plasmids, which, on time averaging, results in equidistribution of the plasmids. Mathematical modeling of ParA and plasmid dynamics support these interpretations. Mutational analysis supports a molecular mechanism in which the ParB/parC complex controls ParA filament depolymerization.
细菌质粒编码赋予质粒稳定遗传的分区(par)位点。我们之前表明,在质粒pB171的par2位点编码的ParB和parC存在的情况下,ParA形成了类似细胞骨架的结构,这些结构在类核上动态重新定位。同时,par2位点将质粒规则地分布在类核上。我们在此表明,动态的ParA模式并非简单的振荡。相反,ParA在质粒之间成核并聚合。当一个ParA聚集体到达一个质粒时,组装反应会逆转为解体。引人注目的是,质粒始终在解体的ParA细胞骨架结构后面迁移,这表明ParA丝通过解聚拉动质粒。ParA组装和解体的持续循环导致质粒不断重新定位,平均而言,这导致了质粒的均匀分布。对ParA和质粒动态的数学建模支持了这些解释。突变分析支持了一种分子机制,即ParB/parC复合物控制ParA丝的解聚。