Transient Membrane-Linked FtsZ Assemblies Precede Z-Ring Formation in Escherichia coli

被引:25
|
作者
Walker, Bryant E. [1 ]
Mannik, Jaana [1 ,2 ]
Mannik, Jaan [1 ]
机构
[1] Univ Tennessee, Dept Phys & Astron, Knoxville, TN 37996 USA
[2] Univ Tennessee, Dept Biochem & Cellular & Mol Biol, Knoxville, TN 37996 USA
基金
美国国家卫生研究院;
关键词
HIGH-THROUGHPUT; CELL; FILAMENTS; DYNAMICS; ZIPA; PROTEIN; ORGANIZATION; POLYMERS; HOMOLOG; TUBULIN;
D O I
10.1016/j.cub.2019.12.023
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During the early stages of cytokinesis, FtsZ protofilaments form a ring-like structure, the Z-ring, in most bacterial species. This cytoskeletal scaffold recruits downstream proteins essential for septa! cell wall synthesis. Despite progress in understanding the dynamic nature of the Z-ring and its role in coordinating septa! cell wall synthesis, the early stages of protofilament formation and subsequent assembly into the Z-ring are still not understood. Here we investigate a sequence of assembly steps that lead to the formation of the Z-ring in Escherichia coli using high temporal and spatial resolution imaging. Our data show that formation of the Z-ring is preceded by transient membrane-linked FtsZ assemblies. These assemblies form after attachment of short cytosolic protofilaments, which we estimate to be less than 20 monomers long, to the membrane. The attachments occur at random locations along the length of the cell. The filaments treadmill and show periods of rapid growth and shrinkage. Their dynamic properties imply that protofilaments are bundled in these assemblies. Furthermore, we establish that the size of assemblies is sensitively controlled by the availability of FtsZ molecules and by the presence of ZapA proteins. The latter has been implicated in cross-linking the protofilaments. The likely function of these dynamic FtsZ assemblies is to sample the cell surface for the proper location for the Z-ring.
引用
收藏
页码:499 / +
页数:16
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