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Dapper, a Dishevelled-associated antagonist of β-catenin and JNK signaling, is required for notochord formation

  • Benjamin N.R. Cheyette
  • , Joshua S. Waxman
  • , Jeffrey R. Miller
  • , Ken Ichi Takemaru
  • , Laird C. Sheldahl
  • , Natasha Khlebtsova
  • , Eric P. Fox
  • , Thomas Earnest
  • , Randall T. Moon
  • Howard Hughes Medical Institute
  • University of Washington
  • Lawrence Berkeley National Laboratory

Research output: Contribution to journal › Article › peer-review

237 Scopus citations

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 languageEnglish
Pages (from-to)449-461
Number of pages13
JournalDevelopmental Cell
Volume2
Issue number4
DOIs
StatePublished - 2002

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