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Bridging of β-catenin and glycogen synthase kinase-3β by Axin and inhibition of β-catenin-mediated transcription
被引:274
|作者:
Sakanaka, C
Weiss, JB
Williams, LT
[1
]
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
[3] Chiron Corp, Emeryville, CA 94608 USA
来源:
关键词:
D O I:
10.1073/pnas.95.6.3020
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
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.
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页码:3020 / 3023
页数:4
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