UBE2L3, a Partner of MuRF1/TRIM63, Is Involved in the Degradation of Myofibrillar Actin and Myosin.


Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
03 08 2021
Historique:
received: 31 03 2021
revised: 21 07 2021
accepted: 28 07 2021
entrez: 27 8 2021
pubmed: 28 8 2021
medline: 18 11 2021
Statut: epublish

Résumé

The ubiquitin proteasome system (UPS) is the main player of skeletal muscle wasting, a common characteristic of many diseases (cancer, etc.) that negatively impacts treatment and life prognosis. Within the UPS, the E3 ligase MuRF1/TRIM63 targets for degradation several myofibrillar proteins, including the main contractile proteins alpha-actin and myosin heavy chain (MHC). We previously identified five E2 ubiquitin-conjugating enzymes interacting with MuRF1, including UBE2L3/UbcH7, that exhibited a high affinity for MuRF1 (K

Identifiants

pubmed: 34440743
pii: cells10081974
doi: 10.3390/cells10081974
pmc: PMC8392593
pii:
doi:

Substances chimiques

Actins 0
Histocompatibility Antigens Class II 0
Muscle Proteins 0
RNA, Small Interfering 0
Tripartite Motif Proteins 0
Dexamethasone 7S5I7G3JQL
Ube2l3 protein, mouse EC 2.3.2.23
Ubiquitin-Conjugating Enzymes EC 2.3.2.23
Trim63 protein, mouse EC 2.3.2.27
Ubiquitin-Protein Ligases EC 2.3.2.27

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Association Française contre les Myopathies
ID : #19521
Organisme : Fondation pour la Recherche Médicale
ID : DEQ20180339180
Organisme : French government IDEX-ISITE initiative CAP 20e25
ID : 16-IDEX-0001
Organisme : European Union's Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement
ID : No 813599

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Auteurs

Dulce Peris-Moreno (D)

Université Clermont Auvergne, INRAE, UNH Unité de Nutrition Humaine, F-63000 Clermont-Ferrand, France.

Mélodie Malige (M)

Université Clermont Auvergne, INRAE, UNH Unité de Nutrition Humaine, F-63000 Clermont-Ferrand, France.

Agnès Claustre (A)

Université Clermont Auvergne, INRAE, UNH Unité de Nutrition Humaine, F-63000 Clermont-Ferrand, France.

Andrea Armani (A)

Department of Biomedical Sciences, Venetian Institute of Molecular Medicine, University of Padua, 35100 Padova, Italy.

Cécile Coudy-Gandilhon (C)

Université Clermont Auvergne, INRAE, UNH Unité de Nutrition Humaine, F-63000 Clermont-Ferrand, France.

Christiane Deval (C)

Université Clermont Auvergne, INRAE, UNH Unité de Nutrition Humaine, F-63000 Clermont-Ferrand, France.

Daniel Béchet (D)

Université Clermont Auvergne, INRAE, UNH Unité de Nutrition Humaine, F-63000 Clermont-Ferrand, France.

Pierre Fafournoux (P)

Université Clermont Auvergne, INRAE, UNH Unité de Nutrition Humaine, F-63000 Clermont-Ferrand, France.

Marco Sandri (M)

Department of Biomedical Sciences, Venetian Institute of Molecular Medicine, University of Padua, 35100 Padova, Italy.

Lydie Combaret (L)

Université Clermont Auvergne, INRAE, UNH Unité de Nutrition Humaine, F-63000 Clermont-Ferrand, France.

Daniel Taillandier (D)

Université Clermont Auvergne, INRAE, UNH Unité de Nutrition Humaine, F-63000 Clermont-Ferrand, France.

Cécile Polge (C)

Université Clermont Auvergne, INRAE, UNH Unité de Nutrition Humaine, F-63000 Clermont-Ferrand, France.

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Classifications MeSH