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Wall mechanics and exocytosis define the shape of growth domains in fission yeast

  • Juan F. Abenza
  • , Etienne Couturier
  • , James Dodgson
  • , Johanna Dickmann
  • , Anatole Chessel
  • , Jacques Dumais
  • , Rafael E. Carazo Salas
  • University of Cambridge
  • University of Cambridge
  • Universidad de Santiago de Chile
  • Universidad Adolfo Ibáñez
  • Harvard University

Résultats de recherche: Contribution à un journalArticleRevue par des pairs

47 Citations (Scopus)

Résumé

The amazing structural variety of cells is matched only by their functional diversity, and reflects the complex interplay between biochemical and mechanical regulation. How both regulatory layers generate specifically shaped cellular domains is not fully understood. Here, we report how cell growth domains are shaped in fission yeast. Based on quantitative analysis of cell wall expansion and elasticity, we develop a model for how mechanics and cell wall assembly interact and use it to look for factors underpinning growth domain morphogenesis. Surprisingly, we find that neither the global cell shape regulators Cdc42-Scd1-Scd2 nor the major cell wall synthesis regulators Bgs1-Bgs4-Rgf1 are reliable predictors of growth domain geometry. Instead, their geometry can be defined by cell wall mechanics and the cortical localization pattern of the exocytic factors Sec6-Syb1-Exo70. Forceful re-directioning of exocytic vesicle fusion to broader cortical areas induces proportional shape changes to growth domains, demonstrating that both features are causally linked.

langue originaleAnglais
Numéro d'article8400
journalNature Communications
Volume6
Les DOIs
étatPublié - 12 oct. 2015
Modification externeOui

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