A condensate dynamic instability orchestrates actomyosin cortex activation

Victoria Tianjing Yan, Arjun Narayanan (), Tina Wiegand, Frank Jülicher () and Stephan W. Grill ()
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Victoria Tianjing Yan: Max Planck Institute of Molecular Cell Biology and Genetics (MPI-CBG)
Arjun Narayanan: Max Planck Institute of Molecular Cell Biology and Genetics (MPI-CBG)
Tina Wiegand: Max Planck Institute of Molecular Cell Biology and Genetics (MPI-CBG)
Frank Jülicher: Max Planck Institute for the Physics of Complex Systems (MPI-PKS)
Stephan W. Grill: Max Planck Institute of Molecular Cell Biology and Genetics (MPI-CBG)

Nature, 2022, vol. 609, issue 7927, 597-604

Abstract: Abstract A key event at the onset of development is the activation of a contractile actomyosin cortex during the oocyte-to-embryo transition1–3. Here we report on the discovery that, in Caenorhabditis elegans oocytes, actomyosin cortex activation is supported by the emergence of thousands of short-lived protein condensates rich in F-actin, N-WASP and the ARP2/3 complex4–8 that form an active micro-emulsion. A phase portrait analysis of the dynamics of individual cortical condensates reveals that condensates initially grow and then transition to disassembly before dissolving completely. We find that, in contrast to condensate growth through diffusion9, the growth dynamics of cortical condensates are chemically driven. Notably, the associated chemical reactions obey mass action kinetics that govern both composition and size. We suggest that the resultant condensate dynamic instability10 suppresses coarsening of the active micro-emulsion11, ensures reaction kinetics that are independent of condensate size and prevents runaway F-actin nucleation during the formation of the first cortical actin meshwork.

Date: 2022
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DOI: 10.1038/s41586-022-05084-3

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