Role that phosphorylation of GSK3 plays in insulin and Wnt signalling defined by knockin analysis

Edward J. McManus, Kei Sakamoto, Laura J. Armit, Leah Ronaldson, Natalia Shpiro, Rodolfo Marquez, Dario R. Alessi

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    513 Citations (Scopus)


    The inactivation of glycogen synthase kinase (GSK)3 has been proposed to play important roles in insulin and Wnt signalling. To define the role that inactivation of GSK3 plays, we generated homozygous knockin mice in which the protein kinase B phosphorylation sites on GSK3a (Ser21) and GSK3ß (Ser9) were changed to Ala. The knockin mice were viable and were not diabetic. Using these mice we show that inactivation of GSK3ß rather than GSK3a is the major route by which insulin activates muscle glycogen synthase. In contrast, we demonstrate that the activation of muscle glycogen synthase by contraction, the stimulation of muscle glucose uptake by insulin, or the activation of hepatic glycogen synthase by glucose do not require GSK3 phosphorylation on Ser21/Ser9. GSK3 also becomes inhibited in the Wnt-signalling pathway, by a poorly defined mechanism. In GSK3a/GSK3ß homozygous knockin cells, Wnt3a induces normal inactivation of GSK3, as judged by the stabilisation of ß-catenin and stimulation of Wnt-dependent transcription. These results establish the function of Ser21/Ser9 phosphorylation in several processes in which GSK3 inactivation has previously been implicated.
    Original languageEnglish
    Pages (from-to)1571-1583
    Number of pages13
    JournalThe EMBO Journal
    Issue number8
    Publication statusPublished - Apr 2005


    • Exercise
    • Glucose transport
    • GSK3 inhibitor AR-A014418
    • PI 3-kinase
    • PKB/Akt


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