| Literature DB >> 11970895 |
Benjamin N R Cheyette1, Joshua S Waxman, Jeffrey R Miller, Ken-Ichi Takemaru, Laird C Sheldahl, Natasha Khlebtsova, Eric P Fox, Thomas Earnest, Randall T Moon.
Abstract
Dapper was isolated in a screen for proteins interacting with Dishevelled, a key factor in Wnt signaling. Dapper and Dishevelled colocalize intracellularly and form a complex with Axin, GSK-3, CKI, and beta-catenin. Overexpression of Dapper increases Axin and GSK-3 in this complex, resulting in decreased soluble beta-catenin and decreased activation of beta-catenin-responsive genes. Dapper also inhibits activation by Dishevelled of c-Jun N-terminal kinase (JNK), a component of beta-catenin-independent Frizzled signaling. Inhibition of Dapper activates both beta-catenin-responsive genes and an AP1-responsive promoter, demonstrating that Dapper is a general Dishevelled antagonist. Depletion of maternal Dapper RNA from Xenopus embryos results in loss of notochord and head structures, demonstrating that Dapper is required for normal vertebrate development.Entities:
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Year: 2002 PMID: 11970895 DOI: 10.1016/s1534-5807(02)00140-5
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270