Casein kinase I epsilon enhances the binding of Dvl-1 to Frat-1 and is essential for Wnt-3a-induced accumulation of beta-catenin

J Biol Chem. 2003 Apr 18;278(16):14066-73. doi: 10.1074/jbc.M213265200. Epub 2003 Jan 28.

Abstract

We demonstrate that Dvl-1, casein kinase I epsilon (CKI epsilon), and Frat-1 activate the Wnt signaling pathway cooperatively. The amino acid region 228-250 of Dvl-1 was necessary for its binding to Frat-1, and the interaction of Dvl-1 with Frat-1 was enhanced by CKI epsilon. Coexpression of Dvl-1 and Frat-1 caused accumulation of beta-catenin synergistically in L cells. Both proteins also activated the transcriptional activity of T-cell factor-4 (Tcf-4) synergistically in human embryonic kidney 293 cells, but coexpression of Dvl-1-(Delta 228-250), which lacks the amino acid region 228-250 from Dvl-1, and Frat-1 did not. Dvl-1, but not Dvl-1-(Delta 228-250), acted synergistically with CKI epsilon to activate Tcf-4. Depletion of CKI epsilon by double-stranded RNA interference in HeLa S3 cells led to the inhibition of Wnt-3a-induced phosphorylation of Dvl and the binding of Dvl-1 to Frat-1. Furthermore, depletion of CKI epsilon reduced the Wnt-3a-induced accumulation of beta-catenin, although it did not affect the basal level of beta-catenin. These results indicate that CKI epsilon-dependent phosphorylation of Dvl enhances the formation of a complex of Dvl-1 with Frat-1 and that this complex leads to the activation of the Wnt signaling pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Animals
  • COS Cells
  • Carrier Proteins*
  • Casein Kinases
  • Cell Line
  • Cytoskeletal Proteins / metabolism*
  • DNA, Complementary / metabolism
  • Dishevelled Proteins
  • Gene Deletion
  • Genes, Dominant
  • HeLa Cells
  • Humans
  • Immunohistochemistry
  • Intracellular Signaling Peptides and Proteins
  • Luciferases / metabolism
  • Mutation
  • Neoplasm Proteins*
  • Phenotype
  • Phosphoproteins / metabolism*
  • Phosphorylation
  • Plasmids / metabolism
  • Protein Binding
  • Protein Kinases / metabolism*
  • Protein Kinases / physiology*
  • Protein Structure, Tertiary
  • Proteins / metabolism*
  • Proto-Oncogene Proteins / metabolism*
  • RNA Interference
  • RNA, Double-Stranded
  • Signal Transduction
  • TCF Transcription Factors
  • Trans-Activators / metabolism*
  • Transcription Factor 7-Like 2 Protein
  • Transcription Factors / metabolism
  • Transcription, Genetic
  • Wnt Proteins
  • Wnt3 Protein
  • Wnt3A Protein
  • Xenopus
  • Xenopus Proteins*
  • beta Catenin

Substances

  • Adaptor Proteins, Signal Transducing
  • CTNNB1 protein, Xenopus
  • CTNNB1 protein, human
  • Carrier Proteins
  • Cytoskeletal Proteins
  • DNA, Complementary
  • DVL1 protein, Xenopus
  • DVL1 protein, human
  • Dishevelled Proteins
  • FRAT1 protein, human
  • Intracellular Signaling Peptides and Proteins
  • Neoplasm Proteins
  • PIAS1 protein, Xenopus
  • Phosphoproteins
  • Proteins
  • Proto-Oncogene Proteins
  • RNA, Double-Stranded
  • TCF Transcription Factors
  • TCF7L2 protein, human
  • Trans-Activators
  • Transcription Factor 7-Like 2 Protein
  • Transcription Factors
  • WNT3A protein, Xenopus
  • WNT3A protein, human
  • Wnt Proteins
  • Wnt3 Protein
  • Wnt3A Protein
  • Xenopus Proteins
  • beta Catenin
  • tcf7l2 protein, Xenopus
  • Luciferases
  • Protein Kinases
  • Casein Kinases