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 β-catenin. Overexpression of Dapper increases Axin and GSK-3 in this complex, resulting in decreased soluble β-catenin and decreased activation of β-catenin-responsive genes. Dapper also inhibits activation by Dishevelled of c-Jun N-terminal kinase (JNK), a component of β-catenin-independent Frizzled signaling. Inhibition of Dapper activates both β-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.
| Original language | English |
|---|---|
| Pages (from-to) | 449-461 |
| Number of pages | 13 |
| Journal | Developmental Cell |
| Volume | 2 |
| Issue number | 4 |
| DOIs | |
| State | Published - 2002 |
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