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Arginine methylation of G3BP1 in response to Wnt3a regulates β-catenin mRNA

  • Stony Brook University

Research output: Contribution to journalArticlepeer-review

74 Scopus citations

Abstract

Wnt/β-catenin signaling is essential for normal mammalian development. Wnt3a activates the Wnt/β-catenin pathway through stabilization of β-catenin; a process in which the phosphoprotein Dishevelled figures prominently. Protein arginine methylation in signaling complexes containing Dishevelled was investigated. Mass spectrometry of a prominent arginine-methylated, Dishevelled-associated protein identified the Ras GTPase activating protein-binding protein 1 G3BP1. Stimulation of totipotent mouse embryonic F9 cells with Wnt3a provoked increased methylation of G3BP1. We show that G3BP1 is a novel Ctnnb1 mRNA binding protein. Methylation of G3BP1 constitutes a molecular switch that regulates Ctnnb1 mRNA in response to Wnt3a. Thus, the protein arginine methylation that targets G3BP1 acts as a novel regulator of Ctnnb1 mRNA.

Original languageEnglish
Pages (from-to)2310-2320
Number of pages11
JournalDevelopment
Volume138
Issue number14
DOIs
StatePublished - Jul 15 2011

Keywords

  • Arginine methylation
  • Dishevelled
  • Frizzled
  • G3BP1
  • Protein arginine methyl transferase
  • RNA binding protein
  • Wnt
  • ß-catenin mRNA

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