Direct binding of the PDZ domain of Dishevelled to a conserved internal sequence in the C-terminal region of Frizzled

Mol Cell. 2003 Nov;12(5):1251-60. doi: 10.1016/s1097-2765(03)00427-1.

Abstract

The cytoplasmic protein Dishevelled (Dvl) and the associated membrane-bound receptor Frizzled (Fz) are essential in canonical and noncanonical Wnt signaling pathways. However, the molecular mechanisms underlying this signaling are not well understood. By using NMR spectroscopy, we determined that an internal sequence of Fz binds to the conventional peptide binding site in the PDZ domain of Dvl; this type of site typically binds to C-terminal binding motifs. The C-terminal region of the Dvl inhibitor Dapper (Dpr) and Frodo bound to the same site. In Xenopus, Dvl binding peptides of Fz and Dpr/Frodo inhibited canonical Wnt signaling and blocked Wnt-induced secondary axis formation in a dose-dependent manner, but did not block noncanonical Wnt signaling mediated by the DEP domain. Together, our results identify a missing molecular connection within the Wnt pathway. Differences in the binding affinity of the Dvl PDZ domain and its binding partners may be important in regulating signal transduction by Dvl.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adaptor Proteins, Signal Transducing*
  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • Body Patterning
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Dishevelled Proteins
  • Drosophila Proteins / chemistry*
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism*
  • Female
  • Frizzled Receptors
  • Homeodomain Proteins / metabolism
  • Humans
  • Membrane Proteins / chemistry*
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Microinjections
  • Models, Molecular
  • Molecular Sequence Data
  • Morphogenesis / physiology
  • Nuclear Proteins*
  • Peptide Fragments / genetics
  • Peptide Fragments / metabolism
  • Phosphoproteins / chemistry*
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism*
  • Protein Binding
  • Protein Structure, Tertiary
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism
  • Receptors, G-Protein-Coupled
  • Sequence Alignment
  • Signal Transduction / physiology
  • Two-Hybrid System Techniques
  • Wnt Proteins
  • Xenopus Proteins / genetics
  • Xenopus Proteins / metabolism
  • Xenopus laevis
  • Zebrafish Proteins*

Substances

  • Adaptor Proteins, Signal Transducing
  • Carrier Proteins
  • DACT1 protein, Xenopus
  • DACT1 protein, human
  • DVL1 protein, Xenopus
  • Dishevelled Proteins
  • Drosophila Proteins
  • Frizzled Receptors
  • Homeodomain Proteins
  • Membrane Proteins
  • Nuclear Proteins
  • Peptide Fragments
  • Phosphoproteins
  • Proto-Oncogene Proteins
  • Receptors, G-Protein-Coupled
  • SIA1 protein, Xenopus
  • Wnt Proteins
  • Xenopus Proteins
  • Zebrafish Proteins
  • dsh protein, Drosophila
  • fz protein, Drosophila

Associated data

  • PDB/1MC7