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G protein signaling from activated rat Frizzled-1 to the β-catenin-lef-tcf pathway

  • T. Liu
  • , A. J. DeCostanzo
  • , X. Liu
  • , H. Wang
  • , S. Hallagan
  • , R. T. Moon
  • , C. C. Malbon
  • Stony Brook University

Research output: Contribution to journalArticlepeer-review

230 Scopus citations

Abstract

The frizzled receptors, which mediate development and display seven hydrophobic, membrane-spanning segments, are cell membrane-localized. We constructed a chimeric receptor with the ligand-binding and transmembrane segments from the β2-adrenergic receptor (β2AR) and the cytoplasmic domains from rat Frizzled-1 (Rfz1), Stimulation of mouse F9 clones expressing the chimera (β2AR-Rfz1) with the β-adrenergic agonist isoproterenol stimulated stabilization of β-catenin, activation of a β-catenin-sensitive promoter, and formation of primitive endoderm. The response was blocked by inactivation of pertussis toxin-sensitive, heterotrimeric guanine nucleotide-binding proteins (G proteins) and by depletion of Gαq and Gαo. Thus, G proteins are elements of Wnt/Frizzled-1 signaling to the β-catenin-lymphoid-enhancer factor (LEF)-T cell factor (Tcf) pathway.

Original languageEnglish
Pages (from-to)1718-1722
Number of pages5
JournalScience
Volume292
Issue number5522
DOIs
StatePublished - Jun 1 2001

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