Myosin Binding Protein-C Slow: An Intricate Subfamily of Proteins

被引:26
|
作者
Ackermann, Maegen A. [1 ]
Kontrogianni-Konstantopoulos, Aikaterini [1 ]
机构
[1] Univ Maryland, Sch Med, Dept Biochem & Mol Biol, Baltimore, MD 21201 USA
基金
美国国家卫生研究院;
关键词
FAMILIAL HYPERTROPHIC CARDIOMYOPATHY; DIGITORUM LONGUS MUSCLES; RABBIT SKELETAL-MUSCLE; FIBER-TYPE COMPOSITION; CARDIAC MYOSIN; MYBP-C; STRIATED-MUSCLE; DIFFERENTIAL EXPRESSION; ISOFORM TRANSITIONS; ACTOMYOSIN ATPASE;
D O I
10.1155/2010/652065
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Myosin binding protein C (MyBP-C) consists of a family of thick filament associated proteins. Three isoforms of MyBP-C exist in striated muscles: cardiac, slow skeletal, and fast skeletal. To date, most studies have focused on the cardiac form, due to its direct involvement in the development of hypertrophic cardiomyopathy. Here we focus on the slow skeletal form, discuss past and current literature, and present evidence to support that: (i) MyBP-C slow comprises a subfamily of four proteins, resulting from complex alternative shuffling of the single MyBP-C slow gene, (ii) the four MyBP-C slow isoforms are expressed in variable amounts in different skeletal muscles, (iii) at least one MyBP-C slow isoform is preferentially found at the periphery of M-bands and (iv) the MyBP-C slow subfamily may play important roles in the assembly and stabilization of sarcomeric M- and A-bands and regulate the contractile properties of the actomyosin filaments.
引用
收藏
页数:10
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