Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A.

Détails

ID Serval
serval:BIB_96F88AC9C57C
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A.
Périodique
Cell
Auteur⸱e⸱s
Richard I., Broux O., Allamand V., Fougerousse F., Chiannilkulchai N., Bourg N., Brenguier L., Devaud C., Pasturaud P., Roudaut C., Hillaire D., Passos-Bueno M.R., Zatz M., Tischfield J.A., Fardeau M., Jackson C.E., Cohen D., Beckmann J.S.
ISSN
0092-8674
Statut éditorial
Publié
Date de publication
04/1995
Peer-reviewed
Oui
Volume
81
Numéro
1
Pages
27-40
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't - Publication Status: ppublish
Résumé
Limb-girdle muscular dystrophies (LGMDs) are a group of inherited diseases whose genetic etiology has yet to be elucidated. The autosomal recessive forms (LGMD2) constitute a genetically heterogeneous group with LGMD2A mapping to chromosome 15q15.1-q21.1. The gene encoding the muscle-specific calcium-activated neutral protease 3 (CANP3) large subunit is located in this region. This cysteine protease belongs to the family of intracellular calpains. Fifteen nonsense, splice site, frameshift, or missense calpain mutations cosegregate with the disease in LGMD2A families, six of which were found within La Réunion island patients. A digenic inheritance model is proposed to account for the unexpected presence of multiple independent mutations in this small inbred population. Finally, these results demonstrate an enzymatic rather than a structural protein defect causing a muscular dystrophy, a defect that may have regulatory consequences, perhaps in signal transduction.
Mots-clé
Amino Acid Sequence, Base Sequence, Calpain/genetics, Chromosomes, Human, Pair 15, DNA/blood, DNA Mutational Analysis, Exons/genetics, Gene Expression, Genetic Screening, Humans, Models, Genetic, Molecular Sequence Data, Muscular Dystrophies/enzymology, Muscular Dystrophies/ethnology, Mutation/genetics, Nucleic Acid Heteroduplexes, Polymerase Chain Reaction/methods, Restriction Mapping, Sequence Alignment
Pubmed
Web of science
Open Access
Oui
Création de la notice
25/01/2008 17:18
Dernière modification de la notice
20/08/2019 15:58
Données d'usage