Home LiteratureArticle Details
PMID: 10441321 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan-deficient mice.

Human molecular genetics ·Vol. 8 ·No. 9 ·1999-09-00 ·Pages 1589-98

Araishi K, Sasaoka T, Imamura M, Noguchi S, Hama H, Wakabayashi E, Yoshida M, Hori T, Ozawa E

Abstract

beta-Sarcoglycan, one of the subunits of the sarcoglycan complex, is a transmembranous glycoprotein which associates with dystrophin and is the molecule responsible for beta-sarcoglycanopathy, a Duchenne-like autosomal recessive muscular dystrophy. To develop an animal model of beta-sarcoglycanopathy and to clarify the role of beta-sarcoglycan in the pathogenesis of the muscle degeneration in vivo, we developed beta-sarcoglycan-deficient mice using a gene targeting technique. beta-Sarcoglycan-deficient mice (BSG(-)(/-)mice) exhibited progressive muscular dystrophy with extensive degeneration and regeneration. The BSG(-)(/-)mice also exhibited muscular hypertrophy characteristic of beta-sarcoglycanopathy. Immunohistochemical and immunoblot analyses of BSG(-)(/-)mice demonstrated that deficiency of beta-sarcoglycan also caused loss of all of the other sarcoglycans as well as of sarcospan in the sarcolemma. On the other hand, laminin-alpha2, alpha- and beta-dystroglycan and dystrophin were still present in the sarcolemma. However, the dystrophin-dystroglycan complex in BSG(-)(/-)mice was unstable compared with that in the wild-type mice. Our data suggest that loss of the sarcoglycan complex and sarcospan alone is sufficient to cause muscular dystrophy, that beta-sarcoglycan is an important protein for formation of the sarcoglycan complex associated with sarcospan and that the role of the sarcoglycan complex and sarcospan may be to strengthen the dystrophin axis connecting the basement membrane with the cytoskeleton.

MeSH Terms
Animals Carrier Proteins/genetics,metabolism Cytoskeletal Proteins/deficiency,genetics Disease Models, Animal Dystroglycans Dystrophin/metabolism Fluorescent Antibody Technique Humans Membrane Glycoproteins/deficiency,genetics Membrane Proteins/genetics,metabolism Mice Mice, Knockout Molecular Sequence Data Muscle Proteins/deficiency,genetics Muscle, Skeletal/metabolism Muscular Dystrophies/genetics Myocardium/cytology Neoplasm Proteins Phenotype RNA, Messenger/metabolism
Chemicals
Carrier Proteins Cytoskeletal Proteins DAG1 protein, human Dystrophin Membrane Glycoproteins Membrane Proteins Muscle Proteins Neoplasm Proteins RNA, Messenger SSPN protein, human Sspn protein, mouse Dystroglycans
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Araishi K
Division of Cell Biology, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Kodaira, Tokyo, 187-8502, Japan.
Sasaoka T
Imamura M
Noguchi S
Hama H
Wakabayashi E
Yoshida M
Hori T
Ozawa E
Article Info
Journal
Human molecular genetics
Abbr.
Hum Mol Genet
ISSN
0964-6906
Published
1999-09-00
Pages
1589-98
Language
English
Region
England
NLM ID
9208958
Subset
IM
Databases
GENBANK
AB024920, AB024921, AB024922, AB024923
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]