Dynamic Opposition of Clustered Proteins Stabilizes Cortical Polarity in the C. elegans Zygote

被引:54
作者
Sailer, Anne [1 ]
Anneken, Alexander [1 ]
Li, Younan [1 ,2 ]
Lee, Sam [5 ]
Munro, Edwin [1 ,2 ,3 ,4 ]
机构
[1] Univ Chicago, Dept Mol Genet & Cell Biol, Chicago, IL 60637 USA
[2] Univ Chicago, Comm Dev Regenerat & Stem Cell Biol, Chicago, IL 60637 USA
[3] Univ Chicago, Inst Biophys Dynam, Chicago, IL 60637 USA
[4] Univ Chicago, Comm Genet Genom & Syst Biol, Chicago, IL 60637 USA
[5] Univ Wisconsin, Dept Med, Madison, WI 53792 USA
关键词
CAENORHABDITIS-ELEGANS; CELL POLARITY; PAR PROTEINS; ASYMMETRIC DIVISION; FUNCTIONAL-ANALYSIS; ADHERENS JUNCTIONS; MAINTAIN POLARITY; EMBRYOS; CDC-42; LOCALIZATION;
D O I
10.1016/j.devcel.2015.09.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dynamic maintenance of cell polarity is essential for development and physiology. Here we combine experiments and modeling to elucidate mechanisms that maintain cortical polarity in the a elegans zygote. We show that polarity is dynamically stabilized by two coupled cross-inhibitory feedback loops: one involves the oligomeric scaffold PAR-3 and the kinase PAR-1, and the other involves CDC-42 and its putative GAP CHIN-1. PAR-3 and CDC-42 are both required locally to recruit PAR-6/PKC-3, which inhibits PAR-1 (shown previously) and inhibits local growth/accumulation of CHIN-1 clusters. Conversely, PAR-1 inhibits local accumulation of PAR-3 oligomers, while CHIN-1 inhibits CDC-42 (shown previously), such that either PAR-1 or CHIN-1 can prevent recruitment of PAR-6/PKC-3, but loss of both causes complete loss of polarity. Ultrasensitive dependence of CHIN-1 cluster growth on PAR-6/PKC-3 endows this core circuit with bistable dynamics, while transport of CHIN-1 clusters by cortical flow can stabilize the AP boundary against diffusive spread of PAR-6/PKC-3.
引用
收藏
页码:131 / 142
页数:12
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