Bi E F, Lutkenhaus J
Department of Microbiology, University of Kansas Medical Center, Kansas City 66103.
Nature. 1991 Nov 14;354(6349):161-4. doi: 10.1038/354161a0.
Genes for cell division have been identified in Escherichia coli by the isolation of conditional lethal mutations that block cell division, but do not affect DNA replication or segregation. Of these genes, ftsZ is of great interest as it acts earliest in the division pathway, is essential, its level dictates the frequency of division, and it is thought to be the target of two cell-division inhibitors, SulA, produced in response to DNA damage, and MinCD, which prevents division at old sites. Here we have used immunoelectronmicroscopy to localize the FtsZ protein to the division site. The results suggest that FtsZ self-assembles into a ring structure at the future division site and may function as a cytoskeletal element. The formation of this ring may be the point at which division is regulated.
通过分离阻断细胞分裂但不影响DNA复制或分离的条件致死突变,已在大肠杆菌中鉴定出细胞分裂相关基因。在这些基因中,ftsZ备受关注,因为它在分裂途径中作用最早,是必需的,其水平决定分裂频率,并且被认为是两种细胞分裂抑制剂的作用靶点,一种是响应DNA损伤产生的SulA,另一种是MinCD,它可防止在旧位点进行分裂。在此,我们利用免疫电子显微镜将FtsZ蛋白定位到分裂位点。结果表明,FtsZ在未来的分裂位点自组装成环形结构,可能作为一种细胞骨架成分发挥作用。这个环的形成可能是调控分裂的关键点。