Frodo links Dishevelled to the p120-catenin/Kaiso pathway: distinct catenin subfamilies promote Wnt signals

Dev Cell. 2006 Nov;11(5):683-95. doi: 10.1016/j.devcel.2006.09.022.

Abstract

p120-catenin is an Arm repeat protein that interacts with varied components such as cadherin, small G proteins, kinases, and the Kaiso transcriptional repressor. Despite recent advances in understanding the roles that p120-catenin and Kaiso play in downstream modulation of Wnt/beta-catenin signaling, the identity of the upstream regulators of the p120-catenin/Kaiso pathway have remained unclear. Here, we find that p120-catenin binds Frodo, which itself interacts with the Wnt pathway protein Dishevelled (Dsh). In Xenopus laevis, we demonstrate that Wnt signals result in Frodo-mediated stabilization of p120-catenin, which, in turn, promotes Kaiso sequestration or removal from the nucleus. Our results point to Dsh and Frodo as upstream regulators of the p120-catenin/Kaiso signaling pathway. Importantly, this suggests that Wnt signals acting through Dsh regulate the stability of p120-catenin in addition to that of beta-catenin, and that each catenin promotes its respective signal in parallel to regulate distinct, as well as shared, direct downstream gene targets.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / metabolism*
  • Animals
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Carrier Proteins / physiology*
  • Catenins
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / metabolism
  • Cell Adhesion Molecules / physiology*
  • Cell Nucleus / metabolism
  • Delta Catenin
  • Dishevelled Proteins
  • Embryo, Nonmammalian
  • In Vitro Techniques
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism*
  • Phosphoproteins / physiology*
  • Protein Binding
  • Protein Transport
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism
  • Repressor Proteins / physiology*
  • Signal Transduction
  • Two-Hybrid System Techniques
  • Wnt Proteins / genetics
  • Wnt Proteins / physiology*
  • Xenopus Proteins / genetics
  • Xenopus Proteins / metabolism
  • Xenopus Proteins / physiology*
  • Xenopus laevis

Substances

  • Adaptor Proteins, Signal Transducing
  • Carrier Proteins
  • Catenins
  • Cell Adhesion Molecules
  • DACT1 protein, Xenopus
  • DVL1 protein, Xenopus
  • Dishevelled Proteins
  • Phosphoproteins
  • Repressor Proteins
  • Wnt Proteins
  • Xenopus Proteins
  • ZBTB33 protein, Xenopus
  • Delta Catenin