Spatially restricted activation of RhoA signalling at epithelial junctions by p114RhoGEF drives junction formation and morphogenesis

  • Stephen J. Terry
  • , Ceniz Zihni
  • , Ahmed Elbediwy
  • , Elisa Vitiello
  • , Isabelle V.Leefa Chong San
  • , Maria S. Balda
  • , Karl Matter

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Signalling by the GTPase RhoA, a key regulator of epithelial cell behaviour, can stimulate opposing processes: RhoA can promote junction formation and apical constriction, and reduce adhesion and cell spreading. Molecular mechanisms are thus required that ensure spatially restricted and process-specific RhoA activation. For many fundamental processes, including assembly of the epithelial junctional complex, such mechanisms are still unknown. Here we show that p114RhoGEF is a junction-associated protein that drives RhoA signalling at the junctional complex and regulates tight-junction assembly and epithelial morphogenesis. p114RhoGEF is required for RhoA activation at cell-cell junctions, and its depletion stimulates non-junctional Rho signalling and induction of myosin phosphorylation along the basal domain. Depletion of GEF-H1, a RhoA activator inhibited by junctional recruitment, does not reduce junction-associated RhoA activation. p114RhoGEF associates with a complex containing myosin II, Rock II and the junctional adaptor cingulin, indicating that p114RhoGEF is a component of a junction-associated Rho signalling module that drives spatially restricted activation of RhoA to regulate junction formation and epithelial morphogenesis.
    Original languageEnglish
    Pages (from-to)159-166
    JournalNature Cell Biology
    Volume13
    Issue number2
    Early online date23 Jan 2011
    DOIs
    Publication statusPublished - 2011

    Bibliographical note

    Note: This research was supported by Fight for Sight and the Wellcome
    Trust.

    Keywords

    • Biological sciences

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