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

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

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          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.

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