Axin directly interacts with plakoglobin and regulates its stability

被引:61
作者
Kodama, S
Ikeda, S
Asahara, T
Kishida, M
Kikuchi, A
机构
[1] Hiroshima Univ, Sch Med, Dept Biochem, Minami Ku, Hiroshima 7348551, Japan
[2] Hiroshima Univ, Sch Med, Dept Surg 2, Minami Ku, Hiroshima 7348551, Japan
关键词
D O I
10.1074/jbc.274.39.27682
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Plakoglobin is homologous to beta-catenin. Axin, a Wnt signal negative regulator, enhances glycogen synthase kinase (GSK)-3 beta-dependent phosphorylation of beta-catenin and stimulates the degradation of beta-catenin. Therefore, we examined the effect of Axin on plakoglobin stability. Axin formed a complex with plakoglobin in COS cells and SW480 cells. Axin directly bound to plakoglobin, and this binding was inhibited by beta-catenin. Axin promoted GSK-3 beta-dependent phosphorylation of plakoglobin. Furthermore, overexpression of Axin down-regulated the level of plakoglobin in SW480 cells. These results suggest that Axin regulates the stability of plakoglobin by enhancing its phosphorylation by GSK-3 beta and that Axin may act on beta-catenin and plakoglobin in similar manners.
引用
收藏
页码:27682 / 27688
页数:7
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