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

•Zygotic polarity is stabilized by two redundant cross-inhibitory feedback loops•PAR-1 opposes PAR-3 clusters; PAR-6/PKC-3 oppose CHIN-1 clusters•Threshold dependence of CHIN-1 cluster growth on PAR-6/PKC-3 yields bistable dynamics•Cortical transport of CHIN-1 and PAR-3 clusters stabilizes AP boundary position

SummaryDynamic 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 C. 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.

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