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

First Author  Bikkavilli RK Year  2011
Journal  J Cell Sci Volume  124
Issue  Pt 13 Pages  2310-20
PubMed ID  21652632 Mgi Jnum  J:183055
Mgi Id  MGI:5317392 Doi  10.1242/jcs.084046
Citation  Bikkavilli RK, et al. (2011) Arginine methylation of G3BP1 in response to Wnt3a regulates beta-catenin mRNA. J Cell Sci 124(Pt 13):2310-20
abstractText  Wnt/beta-catenin signaling is essential for normal mammalian development. Wnt3a activates the Wnt/beta-catenin pathway through stabilization of beta-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.
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