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May 17, 1996Science1,424 citations

Binding of GSK3β to the APC-β-Catenin Complex and Regulation of Complex Assembly

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BRBonnee RubinfeldLawrence Livermore National LaboratoryIAIris AlbertCitrix (Switzerland)EPEmilio PorfiriMarche Polytechnic University

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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.

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Cite This Study

Rubinfeld et al. (1996) studied this question.

synapsesocial.com/papers/69d755d4b4cef8fedc48f643https://doi.org/10.1126/science.272.5264.1023
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