The Roles of NEDD4 Subfamily of HECT E3 Ubiquitin Ligases in Neurodevelopment and Neurodegeneration.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
31 Mar 2022
Historique:
received: 01 02 2022
revised: 28 03 2022
accepted: 29 03 2022
entrez: 12 4 2022
pubmed: 13 4 2022
medline: 14 4 2022
Statut: epublish

Résumé

The ubiquitin pathway regulates the function of many proteins and controls cellular protein homeostasis. In recent years, it has attracted great interest in neurodevelopmental and neurodegenerative diseases. Here, we have presented the first review on the roles of the 9 proteins of the HECT E3 ligase NEDD4 subfamily in the development and function of neurons in the central nervous system (CNS). We discussed their regulation and their direct or indirect involvement in neurodevelopmental diseases, such as intellectual disability, and neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease or Amyotrophic Lateral Sclerosis. Further studies on the roles of these proteins, their regulation and their targets in neurons will certainly contribute to a better understanding of neuronal function and dysfunction, and will also provide interesting information for the development of therapeutics targeting them.

Identifiants

pubmed: 35409239
pii: ijms23073882
doi: 10.3390/ijms23073882
pmc: PMC8999422
pii:
doi:

Substances chimiques

Endosomal Sorting Complexes Required for Transport 0
Ubiquitin 0
Nedd4 Ubiquitin Protein Ligases EC 2.3.2.26
Nedd4 protein, human EC 2.3.2.26
Ubiquitin-Protein Ligases EC 2.3.2.27

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Shanez Haouari (S)

UMR 1253, iBrain, Université de Tours, Inserm, 37044 Tours, France.

Patrick Vourc'h (P)

UMR 1253, iBrain, Université de Tours, Inserm, 37044 Tours, France.
CHRU de Tours, Service de Biochimie et Biologie Moléculaire, 37044 Tours, France.

Médéric Jeanne (M)

UMR 1253, iBrain, Université de Tours, Inserm, 37044 Tours, France.
CHRU de Tours, Service de Génétique, 37044 Tours, France.

Sylviane Marouillat (S)

UMR 1253, iBrain, Université de Tours, Inserm, 37044 Tours, France.

Charlotte Veyrat-Durebex (C)

UMR 1253, iBrain, Université de Tours, Inserm, 37044 Tours, France.
CHRU de Tours, Service de Biochimie et Biologie Moléculaire, 37044 Tours, France.

Débora Lanznaster (D)

UMR 1253, iBrain, Université de Tours, Inserm, 37044 Tours, France.

Frédéric Laumonnier (F)

UMR 1253, iBrain, Université de Tours, Inserm, 37044 Tours, France.

Philippe Corcia (P)

UMR 1253, iBrain, Université de Tours, Inserm, 37044 Tours, France.
CHRU de Tours, Service de Neurologie, 37044 Tours, France.

Hélène Blasco (H)

UMR 1253, iBrain, Université de Tours, Inserm, 37044 Tours, France.
CHRU de Tours, Service de Biochimie et Biologie Moléculaire, 37044 Tours, France.

Christian R Andres (CR)

UMR 1253, iBrain, Université de Tours, Inserm, 37044 Tours, France.
CHRU de Tours, Service de Biochimie et Biologie Moléculaire, 37044 Tours, France.

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