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 language | English |
|---|---|
| Pages (from-to) | 2310-2320 |
| Number of pages | 11 |
| Journal | Development |
| Volume | 138 |
| Issue number | 14 |
| DOIs | |
| State | Published - Jul 15 2011 |
Keywords
- Arginine methylation
- Dishevelled
- Frizzled
- G3BP1
- Protein arginine methyl transferase
- RNA binding protein
- Wnt
- ß-catenin mRNA
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