Gullbrand B, Nordström K
Department of Cell and Molecular Biology, Biomedical Center, Uppsala University, Sweden.
Mol Microbiol. 2000 Jun;36(6):1349-59. doi: 10.1046/j.1365-2958.2000.01949.x.
In this report, we have investigated cell division after inhibition of initiation of chromosome replication in Escherichia coli. In a culture grown to the stationary phase, cells containing more than one chromosome were able to divide some time after restart of growth, under conditions not allowing initiation of chromosome replication. This shows that there is no requirement for cell division to take place within a certain time after initiation of chromosome replication. Continued growth without initiation of replication resulted in filamented cells that generally did not have any constrictions. Interestingly, FtsZ rings were formed in a majority of these cells as they reached a certain cell length. These rings appeared and were maintained for some time at the cell quarter positions on both sides of the centrally localized nucleoid. These results confirm previous findings that cell division sites are formed independently of chromosome replication and indicate that FtsZ ring assembly is dependent on cell size rather than on the capacity of the cell to divide. Disruption of the mukB gene caused a significant increase in the region occupied by DNA after the replication runout, consistent with a role of MukB in chromosome condensation. The aberrant nucleoid structure was accompanied by a shift in FtsZ ring positioning, indicating an effect of the nucleoid on the positioning of the FtsZ ring. A narrow cell length interval was found, under and over which primarily central and non-central FtsZ rings, respectively, were observed. This finding correlates well with the previously observed oscillatory movement of MinC and MinD in short and long cells.
在本报告中,我们研究了大肠杆菌中染色体复制起始受到抑制后的细胞分裂情况。在生长至稳定期的培养物中,含有多条染色体的细胞在重新开始生长后的一段时间内,能够在不允许染色体复制起始的条件下进行分裂。这表明细胞分裂并不需要在染色体复制起始后的特定时间内发生。在不进行复制起始的情况下持续生长会导致形成丝状细胞,这些细胞通常没有任何缢缩。有趣的是,当这些细胞达到一定长度时,大多数细胞中会形成FtsZ环。这些环出现在中央定位的类核两侧的细胞四分之一位置,并维持一段时间。这些结果证实了先前的发现,即细胞分裂位点的形成独立于染色体复制,并表明FtsZ环的组装依赖于细胞大小而非细胞的分裂能力。mukB基因的破坏导致复制耗尽后DNA所占区域显著增加,这与MukB在染色体凝聚中的作用一致。异常的类核结构伴随着FtsZ环定位的改变,表明类核对FtsZ环的定位有影响。发现了一个狭窄的细胞长度区间,在此区间以下和以上分别主要观察到中央和非中央的FtsZ环。这一发现与先前观察到的MinC和MinD在短细胞和长细胞中的振荡运动密切相关。