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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2013
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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. |
format | Online Article Text |
id | pubmed-4177543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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