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Translational control by RGS2

The regulator of G protein signaling (RGS) proteins are a family of guanosine triphosphatase (GTPase)–accelerating proteins. We have discovered a novel function for RGS2 in the control of protein synthesis. RGS2 was found to bind to eIF2Bϵ (eukaryotic initiation factor 2B ϵ subunit) and inhibit the...

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Autores principales: Nguyen, Chau H., Ming, Hong, Zhao, Peishen, Hugendubler, Lynne, Gros, Robert, Kimball, Scot R., Chidiac, Peter
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2742185/
https://www.ncbi.nlm.nih.gov/pubmed/19736320
http://dx.doi.org/10.1083/jcb.200811058
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author Nguyen, Chau H.
Ming, Hong
Zhao, Peishen
Hugendubler, Lynne
Gros, Robert
Kimball, Scot R.
Chidiac, Peter
author_facet Nguyen, Chau H.
Ming, Hong
Zhao, Peishen
Hugendubler, Lynne
Gros, Robert
Kimball, Scot R.
Chidiac, Peter
author_sort Nguyen, Chau H.
collection PubMed
description The regulator of G protein signaling (RGS) proteins are a family of guanosine triphosphatase (GTPase)–accelerating proteins. We have discovered a novel function for RGS2 in the control of protein synthesis. RGS2 was found to bind to eIF2Bϵ (eukaryotic initiation factor 2B ϵ subunit) and inhibit the translation of messenger RNA (mRNA) into new protein. This effect was not observed for other RGS proteins tested. This novel function of RGS2 is distinct from its ability to regulate G protein–mediated signals and maps to a stretch of 37 amino acid residues within its conserved RGS domain. Moreover, RGS2 was capable of interfering with the eIF2–eIF2B GTPase cycle, which is a requisite step for the initiation of mRNA translation. Collectively, this study has identified a novel role for RGS2 in the control of protein synthesis that is independent of its established RGS domain function.
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spelling pubmed-27421852010-03-07 Translational control by RGS2 Nguyen, Chau H. Ming, Hong Zhao, Peishen Hugendubler, Lynne Gros, Robert Kimball, Scot R. Chidiac, Peter J Cell Biol Research Articles The regulator of G protein signaling (RGS) proteins are a family of guanosine triphosphatase (GTPase)–accelerating proteins. We have discovered a novel function for RGS2 in the control of protein synthesis. RGS2 was found to bind to eIF2Bϵ (eukaryotic initiation factor 2B ϵ subunit) and inhibit the translation of messenger RNA (mRNA) into new protein. This effect was not observed for other RGS proteins tested. This novel function of RGS2 is distinct from its ability to regulate G protein–mediated signals and maps to a stretch of 37 amino acid residues within its conserved RGS domain. Moreover, RGS2 was capable of interfering with the eIF2–eIF2B GTPase cycle, which is a requisite step for the initiation of mRNA translation. Collectively, this study has identified a novel role for RGS2 in the control of protein synthesis that is independent of its established RGS domain function. The Rockefeller University Press 2009-09-07 /pmc/articles/PMC2742185/ /pubmed/19736320 http://dx.doi.org/10.1083/jcb.200811058 Text en © 2009 Nguyen et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jcb.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Nguyen, Chau H.
Ming, Hong
Zhao, Peishen
Hugendubler, Lynne
Gros, Robert
Kimball, Scot R.
Chidiac, Peter
Translational control by RGS2
title Translational control by RGS2
title_full Translational control by RGS2
title_fullStr Translational control by RGS2
title_full_unstemmed Translational control by RGS2
title_short Translational control by RGS2
title_sort translational control by rgs2
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2742185/
https://www.ncbi.nlm.nih.gov/pubmed/19736320
http://dx.doi.org/10.1083/jcb.200811058
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