4.7 Article

Frodo links dishevelled to the p120-catenin/Kaiso pathway: Distinct catenin subfamilies promote Wnt signals

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DEVELOPMENTAL CELL
卷 11, 期 5, 页码 683-695

出版社

CELL PRESS
DOI: 10.1016/j.devcel.2006.09.022

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  1. NCI NIH HHS [CA-16672] Funding Source: Medline
  2. NIGMS NIH HHS [R01 GM52112, R01 GM052112] Funding Source: Medline

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p120-catenin is an Arm repeat protein that interacts with varied components such as cadherin, small G proteins, kinases, and the Kalso 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 Kalso 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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