Intracellular localization of P1 ParB protein depends on ParA and parS

被引:94
作者
Erdmann, N [1 ]
Petroff, T [1 ]
Funnell, BE [1 ]
机构
[1] Univ Toronto, Dept Mol & Med Genet, Toronto, ON M5S 1A8, Canada
关键词
D O I
10.1073/pnas.96.26.14905
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The P1 partition system promotes faithful plasmid segregation during the Escherichia coli cell cycle. This system consists of two proteins, ParA and ParB, that act on a plasmid site called parS, By immunofluorescence microscopy, we observed that ParB localizes to discrete foci that are most often located close to the one-quarter and three-quarters positions of cell length, The visualization of ParB foci depended completely on the presence of parS, although their visualization was independent of the chromosomal context of pars (in P1 or the bacterial chromosome). In integration host factor-defective mutants, in which ParB binding to parS is weakened, only a fraction of the total pool of ParB had converged into foci, Taken together, these results indicate that pars recruits a pool of ParB into foci and that the resulting ParB-parS complexes serve as substrates for the segregation reaction. In the absence of ParA, the position of ParB foci in cells is perturbed, indicating that at least one of the roles of ParA is to direct ParB-parS complexes to the proper one-quarter positions from a cell pole. Finally, inhibition of cell division did not inhibit localization of ParB foci in cells, indicating that the positioning signals in the E. coli host that are needed for P1 partition do not depend on early division events.
引用
收藏
页码:14905 / 14910
页数:6
相关论文
共 38 条