Bridging of β-catenin and glycogen synthase kinase-3β by Axin and inhibition of β-catenin-mediated transcription
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作者:
Sakanaka, C
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机构:Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94143 USA
Sakanaka, C
Weiss, JB
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机构:Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94143 USA
Weiss, JB
Williams, LT
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Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94143 USAUniv Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94143 USA
Williams, LT
[1
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机构:
[1] Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94143 USA
[2] Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
Axin antagonizes the developmental effects of Wnt in vertebrates, We show here that Axin simultaneously binds two components of the Wnt pathway, beta-catenin and its negative regulator glycogen synthase kinase-3 beta, In mammalian cells, Axin inhibits Wnt-1 stimulation of beta-catenin/lymphoid enhancer factor 1-dependent transcription, Axin also blocks beta-catenin-mediated transcription in colon cancer cells that have a mutation in the adenomatous polyposis coli gene, These findings suggest that Axin, by forming a complex with beta-catenin and glycogen synthase kinase-3 beta, can block signaling stimulated by Wnt or by adenomatous polyposis coli mutations.