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

被引:77
作者
Park, Jae-il
Ji, Hong
Jun, Sohee
Gu, Dongmin
Hikasa, Hiroki
Li, Lei
Sokol, Sergei Y.
McCrea, Pierre D. [1 ]
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Biochem & Mol Biol, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Program Genes & Dev, Houston, TX 77030 USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Expt Radiat Oncol, Houston, TX 77030 USA
[4] Univ Texas, Grad Sch Biomed Sci, Houston, TX 77030 USA
[5] CUNY Mt Sinai Sch Med, Dept Mol Cell & Dev Biol, New York, NY 10029 USA
关键词
D O I
10.1016/j.devcel.2006.09.022
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:683 / 695
页数:13
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