The Role of Alpha-Dystrobrevin in Striated Muscle

被引:21
作者
Nakamori, Masayuki [1 ,2 ]
Takahashi, Masanori P. [1 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Neurol, Suita, Osaka 5650871, Japan
[2] Univ Rochester, Med Ctr, Dept Neurol, Rochester, NY 14642 USA
来源
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | 2011年 / 12卷 / 03期
基金
日本学术振兴会;
关键词
dystrobrevin; syntrophin; dystrophin; DGC; muscular dystrophy; signaling; intermediate filament; splicing; DYSTROPHIN-GLYCOPROTEIN COMPLEX; NITRIC-OXIDE SYNTHASE; INTERMEDIATE-FILAMENT PROTEINS; LEFT-VENTRICULAR NONCOMPACTION; SKELETAL-MUSCLE; MYOTONIC-DYSTROPHY; MUSCULAR-DYSTROPHY; MESSENGER-RNA; NEUROMUSCULAR DISORDERS; POSTSYNAPTIC PROTEIN;
D O I
10.3390/ijms12031660
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Muscular dystrophies are a group of diseases that primarily affect striated muscle and are characterized by the progressive loss of muscle strength and integrity. Major forms of muscular dystrophies are caused by the abnormalities of the dystrophin glycoprotein complex (DGC) that plays crucial roles as a structural unit and scaffolds for signaling molecules at the sarcolemma. alpha-Dystrobrevin is a component of the DGC and directly associates with dystrophin. alpha-Dystrobrevin also binds to intermediate filaments as well as syntrophin, a modular adaptor protein thought to be involved in signaling. Although no muscular dystrophy has been associated within mutations of the alpha-dystrobrevin gene, emerging findings suggest potential significance of alpha-dystrobrevin in striated muscle. This review addresses the functional role of alpha-dystrobrevin in muscle as well as its possible implication for muscular dystrophy.
引用
收藏
页码:1660 / 1671
页数:12
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