A condensate dynamic instability orchestrates actomyosin cortex activation

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Victoria Tianjing Yan - , Chair of Biophysics, Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Arjun Narayanan - , Chair of Biophysics, Max Planck Institute of Molecular Cell Biology and Genetics, Max-Planck-Institute for the Physics of Complex Systems, Center for Systems Biology Dresden (CSBD) (Author)
  • Tina Wiegand - , Max Planck Institute of Molecular Cell Biology and Genetics, Max-Planck-Institute for the Physics of Complex Systems, Center for Systems Biology Dresden (CSBD) (Author)
  • Frank Jülicher - , Max-Planck-Institute for the Physics of Complex Systems, Center for Systems Biology Dresden (CSBD), TUD Dresden University of Technology (Author)
  • Stephan W. Grill - , Clusters of Excellence PoL: Physics of Life, Biotechnology Center, Max Planck Institute of Molecular Cell Biology and Genetics, Center for Systems Biology Dresden (CSBD) (Author)

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.

Details

Original languageEnglish
Pages (from-to)597-604
Number of pages8
JournalNature
Volume609
Issue number7927
Publication statusPublished - 15 Sept 2022
Peer-reviewedYes

External IDs

PubMed 35978196

Keywords

ASJC Scopus subject areas