Characterization of human junctophilin subtype genes

被引:108
作者
Nishi, M
Mizushima, A
Nakagawara, K
Takeshima, H
机构
[1] Kurume Univ, Inst Life Sci, Div Cell Biol, Fukuoka 8390861, Japan
[2] Univ Tokyo, Fac Med, Dept Pharmacol, Bunkyo Ku, Tokyo 1138654, Japan
[3] Japan Sci & Technol, CREST, Tokyo, Japan
[4] Nihon Gene Res Labs Inc, Miyagino Ku, Sendai, Miyagi 9830034, Japan
关键词
Ca2+ release channel; endoplasmic reticulum; genomic organization; intracellular Ca2+ store; junctophilin; peripheral coupling; ryanodine receptor; sarcoplasmic reticulum; subsurface cisternae; triad junction;
D O I
10.1006/bbrc.2000.3011
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
Junctophilin (JP) subtypes, namely JP-1, 2, and 3, have been currently identified in excitable cells and constitute a novel family of junctional membrane complex proteins. Our studies have suggested that JPs take part in the formation of junctional membrane complexes by spanning the membrane of the intracellular Ca2+ store and interacting with the cell-surface membrane. In this report we describe the primary structures, genomic organization, and tissue distribution of human JP subtypes. By cloning and analyzing human genomic DNA segments, the protein-coding sequence interrupted with four introns was defined in each JP gene, The deduced human JP subtypes shared characteristic structural features with their rabbit and mouse counterparts. Genomic mapping demonstrated that JP genes do not cluster on the human genome. RNA blot hybridization indicated that tissue-specific expression patterns of JP genes in human are essentially the same as those in mouse; skeletal muscle contained both JP-1 and JP-2 mRNAs, the heart predominantly expressed JP-2 mRNA, and the brain specifically contained JP-3 mRNA. In the light of this, we propose intramolecular domains of JP subtypes based on the structural and functional characteristics. (C) 2000 Academic Press.
引用
收藏
页码:920 / 927
页数:8
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