Zeng Q, Subramaniam V N, Wong S H, Tang B L, Parton R G, Rea S, James D E, Hong W
Institute of Molecular and Cell Biology, Singapore 117609, Singapore.
Mol Biol Cell. 1998 Sep;9(9):2423-37. doi: 10.1091/mbc.9.9.2423.
cDNA clones encoding a novel protein (VAMP5) homologous to synaptobrevins/VAMPs are detected during database searches. The predicted 102-amino acid VAMP5 harbors a 23-residue hydrophobic region near the carboxyl terminus and exhibits an overall amino acid identity of 33% with synaptobrevin/VAMP1 and 2 and cellubrevin. Northern blot analysis reveals that the mRNA for VAMP5 is preferentially expressed in the skeletal muscle and heart, whereas significantly lower levels are detected in several other tissues but not in the brain. During in vitro differentiation (myogenesis) of C2C12 myoblasts into myotubes, the mRNA level for VAMP5 is increased approximately 8- to 10-fold. Immunoblot analysis using antibodies specific for VAMP5 shows that the protein levels are also elevated approximately 6-fold during in vitro myogenesis of C2C12 cells. Indirect immunofluorescence microscopy and immunoelectron microscopy reveal that VAMP5 is associated with the plasma membrane as well as intracellular perinuclear and peripheral vesicular structures of myotubes. Epitope-tagged versions of VAMP5 are similarly targeted to the plasma membrane.
在数据库搜索过程中检测到编码一种与突触小泡蛋白/囊泡相关膜蛋白(VAMP)同源的新型蛋白质(VAMP5)的cDNA克隆。预测的102个氨基酸的VAMP5在羧基末端附近有一个23个残基的疏水区域,与突触小泡蛋白/VAMP1、2以及细胞ubrevin的氨基酸序列整体一致性为33%。Northern印迹分析表明,VAMP5的mRNA在骨骼肌和心脏中优先表达,而在其他几种组织中检测到的水平明显较低,但在脑中未检测到。在C2C12成肌细胞体外分化(成肌)为肌管的过程中,VAMP5的mRNA水平增加了约8至10倍。使用针对VAMP5的特异性抗体进行的免疫印迹分析表明,在C2C12细胞体外成肌过程中,蛋白质水平也升高了约6倍。间接免疫荧光显微镜和免疫电子显微镜显示,VAMP5与肌管质膜以及细胞内核周和周边囊泡结构相关。VAMP5的表位标记版本同样定位于质膜。