Department of Ecophysiology, Max Planck Institute for Terrestrial Microbiology, Marburg, Germany.
PLoS Genet. 2013;9(9):e1003802. doi: 10.1371/journal.pgen.1003802. Epub 2013 Sep 19.
Cells closely coordinate cell division with chromosome replication and segregation; however, the mechanisms responsible for this coordination still remain largely unknown. Here, we analyzed the spatial arrangement and temporal dynamics of the 9.1 Mb circular chromosome in the rod-shaped cells of Myxococcus xanthus. For chromosome segregation, M. xanthus uses a parABS system, which is essential, and lack of ParB results in chromosome segregation defects as well as cell divisions over nucleoids and the formation of anucleate cells. From the determination of the dynamic subcellular location of six genetic loci, we conclude that in newborn cells ori, as monitored following the ParB/parS complex, and ter regions are localized in the subpolar regions of the old and new cell pole, respectively and each separated from the nearest pole by approximately 1 µm. The bulk of the chromosome is arranged between the two subpolar regions, thus leaving the two large subpolar regions devoid of DNA. Upon replication, one ori region remains in the original subpolar region while the second copy segregates unidirectionally to the opposite subpolar region followed by the rest of the chromosome. In parallel, the ter region of the mother chromosome relocates, most likely passively, to midcell, where it is replicated. Consequently, after completion of replication and segregation, the two chromosomes show an ori-ter-ter-ori arrangement with mirror symmetry about a transverse axis at midcell. Upon completion of segregation of the ParB/parS complex, ParA localizes in large patches in the DNA-free subpolar regions. Using an Ssb-YFP fusion as a proxy for replisome localization, we observed that the two replisomes track independently of each other from a subpolar region towards ter. We conclude that M. xanthus chromosome arrangement and dynamics combine features from previously described systems with new features leading to a novel spatiotemporal arrangement pattern.
细胞密切协调细胞分裂与染色体复制和分离;然而,负责这种协调的机制在很大程度上仍然未知。在这里,我们分析了杆状细胞中 9.1Mb 环状染色体的空间排列和时间动态。对于染色体分离,粘细菌使用 parABS 系统,这是必不可少的,缺乏 ParB 会导致染色体分离缺陷以及核分裂和无核细胞的形成。从六个遗传基因座的动态亚细胞位置的确定,我们得出结论,在新出生的细胞中,ori,如 ParB/parS 复合物监测,和 ter 区域分别定位于旧和新细胞极的亚极区域,并且每个区域与最近的极分离约 1µm。染色体的大部分排列在两个亚极区域之间,因此留下两个大的亚极区域没有 DNA。在复制时,一个 ori 区域留在原始的亚极区域,而第二个副本单向分离到相反的亚极区域,然后是其余的染色体。平行地,母染色体的 ter 区域重新定位,很可能是被动的,到细胞中部,在那里它被复制。因此,在复制和分离完成后,两个染色体显示出 ori-ter-ter-ori 排列,关于细胞中部的横向轴对称。ParB/parS 复合物完成分离后,ParA 定位于无 DNA 的亚极区域中的大斑块中。使用 Ssb-YFP 融合作为复制体定位的替代物,我们观察到两个复制体独立地从亚极区域向 ter 跟踪。我们得出的结论是,粘细菌染色体的排列和动态结合了先前描述的系统的特征,以及导致新的时空排列模式的新特征。