Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate
Détails
ID Serval
serval:BIB_8E0F28711155
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate
Périodique
Neuromuscular Disorders
ISSN
0960-8966 (Print)
Statut éditorial
Publié
Date de publication
02/1998
Volume
8
Numéro
1
Pages
30-8
Notes
Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S. --- Old month value: Feb
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S. --- Old month value: Feb
Résumé
The sarcoglycan complex is involved in the etiology of four autosomal recessive limb-girdle muscular dystrophies (LGMD2C-F). A missense mutation (T151R) in the beta-sarcoglycan gene on chromosome 4q12 has been shown to cause a mild form of LGMD2E in 11 families from a Southern Indiana Amish community sharing a common haplotype. We now report that two sibs from another Amish family with mild LGMD2E are compound heterozygotes for chromosome 4q12 markers. In order to characterize the genetic defect in this new family, we determined the genomic organization of the beta-sarcoglycan gene. A second missense mutation (R91C) has now been identified in this LGMD2E Amish family. This mutation is also present in the homozygous state in another family of probable Amish ancestry. Finally, analysis of all the components of the dystrophin-glycoprotein complex was performed for the first time on a biopsy from a patient homozygous for the beta-sarcoglycan mutation (T151R). Interestingly, in addition to the loss of the entire sarcoglycan complex, we detected a reduction of alpha-dystroglycan which suggests a role for the sarcoglycan complex in stabilizing alpha-dystroglycan at the sarcolemma.
Mots-clé
Adolescent
Adult
Alternative Splicing
Base Sequence
Child
Chromosome Mapping
*Chromosomes, Human, Pair 4
Cytoskeletal Proteins/*genetics
Dystroglycans
Dystrophin
Ethnic Groups/*genetics
Exons
Female
Genes, Recessive
Haplotypes
Heterozygote Detection
Homozygote
Humans
Hypertrophy
Indiana
Introns
Male
Membrane Glycoproteins/*genetics
Middle Aged
Muscle, Skeletal/pathology
Muscular Dystrophies/*genetics/pathology/physiopathology
Nuclear Family
*Point Mutation
Pubmed
Web of science
Création de la notice
25/01/2008 16:18
Dernière modification de la notice
20/08/2019 14:52