Demarre Gaëlle, Galli Elisa, Muresan Leila, Paly Evelyne, David Ariane, Possoz Christophe, Barre François-Xavier
CNRS, Centre de Génétique Moléculaire, Gif-sur-Yvette, France; Université Paris-Sud, Orsay, France.
PLoS Genet. 2014 Sep 25;10(9):e1004557. doi: 10.1371/journal.pgen.1004557. eCollection 2014 Sep.
The replication terminus region (Ter) of the unique chromosome of most bacteria locates at mid-cell at the time of cell division. In several species, this localization participates in the necessary coordination between chromosome segregation and cell division, notably for the selection of the division site, the licensing of the division machinery assembly and the correct alignment of chromosome dimer resolution sites. The genome of Vibrio cholerae, the agent of the deadly human disease cholera, is divided into two chromosomes, chrI and chrII. Previous fluorescent microscopy observations suggested that although the Ter regions of chrI and chrII replicate at the same time, chrII sister termini separated before cell division whereas chrI sister termini were maintained together at mid-cell, which raised questions on the management of the two chromosomes during cell division. Here, we simultaneously visualized the location of the dimer resolution locus of each of the two chromosomes. Our results confirm the late and early separation of chrI and chrII Ter sisters, respectively. They further suggest that the MatP/matS macrodomain organization system specifically delays chrI Ter sister separation. However, TerI loci remain in the vicinity of the cell centre in the absence of MatP and a genetic assay specifically designed to monitor the relative frequency of sister chromatid contacts during constriction suggest that they keep colliding together until the very end of cell division. In contrast, we found that even though it is not able to impede the separation of chrII Ter sisters before septation, the MatP/matS macrodomain organization system restricts their movement within the cell and permits their frequent interaction during septum constriction.
大多数细菌独特染色体的复制终止区(Ter)在细胞分裂时位于细胞中部。在几个物种中,这种定位参与了染色体分离和细胞分裂之间的必要协调,特别是对于分裂位点的选择、分裂机器组装的许可以及染色体二聚体解析位点的正确排列。霍乱弧菌是致命人类疾病霍乱的病原体,其基因组分为两条染色体,即染色体I(chrI)和染色体II(chrII)。先前的荧光显微镜观察表明,尽管chrI和chrII的Ter区域同时复制,但chrII姐妹端粒在细胞分裂前分离,而chrI姐妹端粒在细胞中部保持在一起,这引发了关于细胞分裂过程中两条染色体管理的问题。在这里,我们同时可视化了两条染色体各自的二聚体解析位点的位置。我们的结果分别证实了chrI和chrII Ter姐妹端粒的晚期和早期分离。它们进一步表明,MatP/matS宏结构域组织系统特别延迟了chrI Ter姐妹端粒的分离。然而,在没有MatP的情况下,TerI位点仍保留在细胞中心附近,并且专门设计用于监测收缩过程中姐妹染色单体接触相对频率的遗传分析表明,它们一直碰撞在一起直到细胞分裂的最后。相比之下,我们发现,尽管MatP/matS宏结构域组织系统在隔膜形成前无法阻止chrII Ter姐妹端粒的分离,但它限制了它们在细胞内的移动,并允许它们在隔膜收缩期间频繁相互作用。