Binding of GSK3 beta to the APC-beta-catenin complex and regulation of complex assembly

被引:1262
作者
Rubinfeld, B
Albert, I
Porfiri, E
Fiol, C
Munemitsu, S
Polakis, P
机构
[1] ONYX PHARMACEUT,RICHMOND,CA 94806
[2] INDIANA UNIV,SCH MED,DEPT BIOCHEM & MOLEC BIOL,INDIANAPOLIS,IN 46202
关键词
D O I
10.1126/science.272.5264.1023
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The adenomatous polyposis coli gene (APC) is mutated in most colon cancers. The APC protein binds lo the cellular adhesion molecule beta-catenin, which is a mammalian homolog of ARMADILLO, a component of the WINGLESS signaling pathway in Drosophila development. Here it is shown that when beta-catenin is present in excess, APC binds to another component of the WINGLESS pathway, glycogen synthase kinase 3 beta (GSK3 beta), a mammalian homolog of Drosophila ZESTE WHITE 3. APC was a good substrate for GSK3 beta in vitro, and the phosphorylation sites were mapped to the central region of APC. Binding of beta-catenin to this region was dependent on phosphorylation by GSK3 beta.
引用
收藏
页码:1023 / 1026
页数:4
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