Ebersbach Gitte, Gerdes Kenn
Department of Biochemistry and Molecular Biology, Campusvej 55, DK-5230 Odense M, University of Southern Denmark, Denmark.
Mol Microbiol. 2004 Apr;52(2):385-98. doi: 10.1111/j.1365-2958.2004.04002.x.
The par2 locus of Escherichia coli plasmid pB171 encodes oscillating ATPase ParA, DNA binding protein ParB and two cis-acting DNA regions to which ParB binds (parC1 and parC2). Three independent techniques were used to investigate the subcellular localization of plasmids carrying par2. In cells with a single plasmid focus, the focus located preferentially at mid-cell. In cells with two foci, these located at quarter-cell positions. In the absence of ParB and parC1/parC2, ParA-GFP formed stationary helices extending from one end of the nucleoid to the other. In the presence of ParB and parC1/parC2, ParA-GFP oscillated in spiral-shaped structures. Amino acid substitutions in ParA simultaneously abolished ParA spiral formation, oscillation and either plasmid localization or plasmid separation at mid-cell. Therefore, our results suggest that ParA spirals position plasmids at the middle of the bacterial nucleoid and subsequently separate them into daughter cells.
大肠杆菌质粒pB171的par2位点编码振荡型ATP酶ParA、DNA结合蛋白ParB以及ParB结合的两个顺式作用DNA区域(parC1和parC2)。运用三种独立技术研究携带par2的质粒的亚细胞定位。在具有单个质粒聚集点的细胞中,该聚集点优先位于细胞中部。在具有两个聚集点的细胞中,它们位于细胞四分之一处的位置。在没有ParB和parC1/parC2的情况下,ParA-GFP形成从类核一端延伸至另一端的固定螺旋。在有ParB和parC1/parC2存在时,ParA-GFP在螺旋状结构中振荡。ParA中的氨基酸替换同时消除了ParA螺旋形成、振荡以及质粒在细胞中部的定位或分离。因此,我们的结果表明,ParA螺旋将质粒定位在细菌类核的中部,随后将它们分离到子细胞中。