Spatiotemporal Regulation of RhoA during Cytokinesis

被引:114
作者
Basant, Angika [1 ]
Glotzer, Michael [2 ]
机构
[1] Francis Crick Inst, London, England
[2] Univ Chicago, Dept Mol Genet & Cell Biol, Chicago, IL 60637 USA
关键词
GTPASE-ACTIVATING PROTEIN; CLEAVAGE FURROW FORMATION; CHROMOSOME PASSENGER COMPLEX; CENTRAL-SPINDLE FORMATION; AURORA-B; CONTRACTILE RING; MITOTIC SPINDLE; RHOGEF ECT2; STRUCTURAL BASIS; PLASMA-MEMBRANE;
D O I
10.1016/j.cub.2018.03.045
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
The active form of the small GTPase RhoA is necessary and sufficient for formation of a cytokinetic furrow in animal cells. Despite the conceptual simplicity of the process, the molecular mechanisms that control it are intricate and involve redundancy at multiple levels. Here, we discuss our current knowledge of the mechanisms underlying spatiotemporal regulation of RhoA during cytokinesis by upstream activators. The direct upstream activator, the RhoGEF Ect2, requires activation due to autoinhibition. Ect2 is primarily activated by the centralspindlin complex, which contains numerous domains that regulate its subcellular localization, oligomeric state, and Ect2 activation. We review the functions of these domains and how centralspindlin is regulated to ensure correctly timed, equatorial RhoA activation. Highlighting recent evidence, we propose that although centralspindlin does not always prominently accumulate on the plasma membrane, it is the site where it promotes RhoA activation during cytokinesis.
引用
收藏
页码:R570 / R580
页数:11
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