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XB-ART-8093
J Biol Chem 2002 Jan 18;2773:2176-85. doi: 10.1074/jbc.M109462200.
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Identification of the Axin and Frat binding region of glycogen synthase kinase-3.

Fraser E , Young N , Dajani R , Franca-Koh J , Ryves J , Williams RS , Yeo M , Webster MT , Richardson C , Smalley MJ , Pearl LH , Harwood A , Dale TC .


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Glycogen synthase kinase-3 (GSK-3) is a key component of several signaling pathways including those regulated by Wnt and insulin ligands. Specificity in GSK-3 signaling is thought to involve interactions with scaffold proteins that localize GSK-3 regulators and substrates. This report shows that GSK-3 forms a low affinity homodimer that is disrupted by binding to Axin and Frat. Based on the crystal structure of GSK-3, we have used surface-scanning mutagenesis to identify residues that differentially affect GSK-3 interactions. Mutations that disrupt Frat and Axin cluster at the dimer interface explaining their effect on homodimer formation. Loss of the Axin binding site blocks the ability of dominant negative GSK-3 to cause axis duplication in Xenopus embryos. The Axin binding site is conserved within all GSK-3 proteins, and its loss affects both cell motility and gene expression in the nonmetazoan, Dictyostelium. Surprisingly, we find no genetic interaction between a non-Axin-binding GSK-3 mutant and T-cell factor activity, arguing that Axin interactions alone cannot explain the regulation of T-cell factor-mediated gene expression.

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Species referenced: Xenopus
Genes referenced: gsk3b gys1 ins