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Publication : Functional interaction of an axin homolog, conductin, with beta-catenin, APC, and GSK3beta.

First Author  Behrens J Year  1998
Journal  Science Volume  280
Issue  5363 Pages  596-9
PubMed ID  9554852 Mgi Jnum  J:47363
Mgi Id  MGI:1203346 Doi  10.1126/science.280.5363.596
Citation  Behrens J, et al. (1998) Functional interaction of an axin homolog, conductin, with beta-catenin, APC, and GSK3beta. Science 280(5363):596-9
abstractText  Control of stability of beta-catenin is central in the wnt signaling pathway. Here, the protein conductin was found to form a complex with both beta-catenin and the tumor suppressor gene product adenomatous polyposis coli (APC). Conductin induced beta-catenin degradation, whereas mutants of conductin that were deficient in complex formation stabilized beta-catenin. Fragments of APC that contained a conductin-binding domain also blocked beta-catenin degradation. Thus, conductin is a component of the multiprotein complex that directs beta-catenin to degradation and is located downstream of APC. In Xenopus embryos, conductin interfered with wnt-induced axis formation.
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