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MG53′s new identity

Mitsugumin 53 (MG53) is a relatively newly identified tripartite motif-containing (TRIM) family muscle-specific E3 ubiquitin ligase that is expressed in skeletal muscle and the heart. It has been postulated to facilitate repair by targeting the site of an injury, and acting as a scaffold for assembl...

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Detalles Bibliográficos
Autores principales: Levy, Jennifer R, Campbell, Kevin P, Glass, David J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4177543/
https://www.ncbi.nlm.nih.gov/pubmed/24175977
http://dx.doi.org/10.1186/2044-5040-3-25
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author Levy, Jennifer R
Campbell, Kevin P
Glass, David J
author_facet Levy, Jennifer R
Campbell, Kevin P
Glass, David J
author_sort Levy, Jennifer R
collection PubMed
description Mitsugumin 53 (MG53) is a relatively newly identified tripartite motif-containing (TRIM) family muscle-specific E3 ubiquitin ligase that is expressed in skeletal muscle and the heart. It has been postulated to facilitate repair by targeting the site of an injury, and acting as a scaffold for assembly of a repair complex made up of dysferlin, annexin V, caveolin-3, and polymerase I and transcript release factor (PTRF). A recent letter published in Nature by Song et al. proposes an alternate function for MG53: as an E3 ligase that targets the insulin receptor and insulin receptor substrate 1 (IRS1) for degradation, therefore regulating muscle insulin signaling. This work is exciting, as it not only presents a novel role for MG53, but also suggests that muscle insulin signaling has a systemic influence on insulin resistance and the metabolic syndrome.
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spelling pubmed-41775432014-09-29 MG53′s new identity Levy, Jennifer R Campbell, Kevin P Glass, David J Skelet Muscle Commentary Mitsugumin 53 (MG53) is a relatively newly identified tripartite motif-containing (TRIM) family muscle-specific E3 ubiquitin ligase that is expressed in skeletal muscle and the heart. It has been postulated to facilitate repair by targeting the site of an injury, and acting as a scaffold for assembly of a repair complex made up of dysferlin, annexin V, caveolin-3, and polymerase I and transcript release factor (PTRF). A recent letter published in Nature by Song et al. proposes an alternate function for MG53: as an E3 ligase that targets the insulin receptor and insulin receptor substrate 1 (IRS1) for degradation, therefore regulating muscle insulin signaling. This work is exciting, as it not only presents a novel role for MG53, but also suggests that muscle insulin signaling has a systemic influence on insulin resistance and the metabolic syndrome. BioMed Central 2013-11-01 /pmc/articles/PMC4177543/ /pubmed/24175977 http://dx.doi.org/10.1186/2044-5040-3-25 Text en Copyright © 2013 Levy et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Commentary
Levy, Jennifer R
Campbell, Kevin P
Glass, David J
MG53′s new identity
title MG53′s new identity
title_full MG53′s new identity
title_fullStr MG53′s new identity
title_full_unstemmed MG53′s new identity
title_short MG53′s new identity
title_sort mg53′s new identity
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4177543/
https://www.ncbi.nlm.nih.gov/pubmed/24175977
http://dx.doi.org/10.1186/2044-5040-3-25
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