Skip to Content
MilliporeSigma
  • Binding of GSK3beta to the APC-beta-catenin complex and regulation of complex assembly.

Binding of GSK3beta to the APC-beta-catenin complex and regulation of complex assembly.

Science (New York, N.Y.) (1996-05-17)
B Rubinfeld, I Albert, E Porfiri, C Fiol, S Munemitsu, P Polakis
ABSTRACT

The adenomatous polyposis coli gene (APC) is mutated in most colon cancers. The APC protein binds to 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 3beta (GSK3beta), 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.