PUBLICATION

Interaction of a Wnt and a Frizzled homologue triggers G-protein-linked phosphatidylinositol signaling

Authors
Slusarski, D., V. Corces, and R. Moon
ID
ZDB-PUB-980916-1
Date
1997
Source
Nature   390: 410-413 (Journal)
Registered Authors
Moon, Randall T., Slusarski, Diane C.
Keywords
none
MeSH Terms
  • Animals
  • Calcium/metabolism
  • Diphosphonates/pharmacology
  • Embryo, Nonmammalian
  • Enzyme Inhibitors/pharmacology
  • Frizzled Receptors
  • GTP-Binding Proteins/drug effects
  • GTP-Binding Proteins/metabolism*
  • Guanosine Diphosphate/analogs & derivatives
  • Guanosine Diphosphate/pharmacology
  • Humans
  • Pertussis Toxin
  • Phosphatidylinositols/metabolism*
  • Phosphoric Monoester Hydrolases/antagonists & inhibitors
  • Proteins/metabolism*
  • Rats
  • Receptors, G-Protein-Coupled
  • Receptors, Neurotransmitter/genetics
  • Receptors, Neurotransmitter/metabolism*
  • Recombinant Proteins/pharmacology
  • Signal Transduction*/drug effects
  • Thionucleotides/pharmacology
  • Virulence Factors, Bordetella/pharmacology
  • Wnt Proteins
  • Xenopus Proteins*
  • Zebrafish
PubMed
9389482 Full text @ Nature
Abstract
In Drosophila, members of the frizzled family of tissue-polarity genes encode proteins that are likely to function as cell-surface receptors of the type known as Wnt receptors, and to initiate signal transduction across the cell membrane, although how they do this is unclear. We show here that the rat protein Frizzled-2 causes an increase in the release of intracellular calcium which is enhanced by Xwnt-5a, a member of the Wnt family. This release of intracellular calcium is suppressed by an inhibitor of the enzyme inositol monophosphatase and hence of the phosphatidylinositol signalling pathway; this suppression can be rescued by injection of the compound myo-inositol, which overcomes the decrease in this intermediate caused by the inhibitor. Agents that inhibit specific G-protein subunits, pertussis toxin, GDP-beta-S and alpha-transducin also inhibit the calcium release triggered by Xwnt-5a and rat Frizzled-2. Our results indicate that some Wnt proteins work through specific Frizzled homologues to stimulate the phosphatidylinositol signalling pathway via heterotrimeric G-protein subunits.
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Human Disease / Model
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