Harry Elizabeth J, Lewis Peter J
School of Molecular and Microbial Biosciences, University of Sydney, Sydney, NSW 2006, Australia.
Mol Microbiol. 2003 Jan;47(1):37-48. doi: 10.1046/j.1365-2958.2003.03253.x.
The earliest event in bacterial cell division is the assembly of a tubulin-like protein, FtsZ, at mid-cell to form a ring. In rod-shaped bacteria, the Min system plays an important role in division site placement by inhibiting FtsZ ring formation specifically at the polar regions of the cell. The Min system comprises MinD and MinC, which form an inhibitor complex and, in Bacillus subtilis, DivIVA, which ensures that division is inhibited only in the polar regions. All three proteins localize to the division site at mid-cell and to cell poles. Their recruitment to the division site is dependent on localization of both 'early' and 'late' division proteins. We have examined the temporal and spatial localization of DivIVA relative to that of FtsZ during the first and second cell division after germination and outgrowth of B. subtilis spores. We show that, although the FtsZ ring assembles at mid-cell about halfway through the cell cycle, DivIVA assembles at this site immediately before cell division and persists there during Z-ring constriction and completion of division. We also show that both DivIVA and MinD localize to the cell poles immediately upon spore germination, well before a Z ring forms at mid-cell. Furthermore, these proteins were found to be present in mature, dormant spores. These results suggest that targeting of Min proteins to division sites does not depend directly on the assembly of the division apparatus, as suggested previously, and that potential polar division sites are blocked at the earliest possible stage in the cell cycle in germinated spores as a mechanism to ensure that equal-sized daughter cells are produced upon cell division.
细菌细胞分裂最早发生的事件是一种微管蛋白样蛋白FtsZ在细胞中部组装形成一个环。在杆状细菌中,Min系统通过特异性抑制FtsZ环在细胞极区的形成,在分裂位点定位中发挥重要作用。Min系统由MinD和MinC组成,它们形成一个抑制复合物,在枯草芽孢杆菌中,还有DivIVA,它确保仅在极区抑制分裂。这三种蛋白都定位于细胞中部的分裂位点以及细胞极。它们被招募到分裂位点取决于“早期”和“晚期”分裂蛋白的定位。我们研究了枯草芽孢杆菌孢子萌发和生长后第一次和第二次细胞分裂过程中DivIVA相对于FtsZ的时间和空间定位。我们发现,虽然FtsZ环在细胞周期大约一半时在细胞中部组装,但DivIVA在细胞分裂前立即在该位点组装,并在Z环收缩和分裂完成期间持续存在于此。我们还发现,DivIVA和MinD在孢子萌发后立即定位于细胞极,远早于细胞中部形成Z环。此外,这些蛋白在成熟的休眠孢子中也存在。这些结果表明,Min蛋白靶向分裂位点并不像之前所认为的那样直接依赖于分裂装置的组装,并且在萌发的孢子中,潜在的极区分裂位点在细胞周期的最早阶段就被阻断,作为一种确保细胞分裂时产生大小相等的子细胞的机制。