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

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 i...

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Detalles Bibliográficos
Autores principales: Bikkavilli, Rama Kamesh, Malbon, Craig C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Company of Biologists 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3113675/
https://www.ncbi.nlm.nih.gov/pubmed/21652632
http://dx.doi.org/10.1242/jcs.084046
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author Bikkavilli, Rama Kamesh
Malbon, Craig C.
author_facet Bikkavilli, Rama Kamesh
Malbon, Craig C.
author_sort Bikkavilli, Rama Kamesh
collection PubMed
description 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.
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spelling pubmed-31136752011-07-01 Arginine methylation of G3BP1 in response to Wnt3a regulates β-catenin mRNA Bikkavilli, Rama Kamesh Malbon, Craig C. J Cell Sci Research Articles 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. Company of Biologists 2011-07-01 /pmc/articles/PMC3113675/ /pubmed/21652632 http://dx.doi.org/10.1242/jcs.084046 Text en © 2011. http://creativecommons.org/licenses/by-nc-sa/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial Share Alike License (http://creativecommons.org/licenses/by-nc-sa/3.0), which permits unrestricted non-commercial use, distribution and reproduction in any medium provided that the original work is properly cited and all further distributions of the work or adaptation are subject to the same Creative Commons License terms.
spellingShingle Research Articles
Bikkavilli, Rama Kamesh
Malbon, Craig C.
Arginine methylation of G3BP1 in response to Wnt3a regulates β-catenin mRNA
title Arginine methylation of G3BP1 in response to Wnt3a regulates β-catenin mRNA
title_full Arginine methylation of G3BP1 in response to Wnt3a regulates β-catenin mRNA
title_fullStr Arginine methylation of G3BP1 in response to Wnt3a regulates β-catenin mRNA
title_full_unstemmed Arginine methylation of G3BP1 in response to Wnt3a regulates β-catenin mRNA
title_short Arginine methylation of G3BP1 in response to Wnt3a regulates β-catenin mRNA
title_sort arginine methylation of g3bp1 in response to wnt3a regulates β-catenin mrna
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3113675/
https://www.ncbi.nlm.nih.gov/pubmed/21652632
http://dx.doi.org/10.1242/jcs.084046
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