Choi O H, Park C S, Itoh K, Adelstein R S, Beaven M A
Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892-1760, USA.
J Muscle Res Cell Motil. 1996 Feb;17(1):69-77. doi: 10.1007/BF00140325.
The complete amino acid sequence (1961 amino acids) of a vertebrate cellular myosin heavy chain-A was deduced from cDNA clones of a secretory rat mast cell line, the RBL-2H3 cell. The rat, human and chicken cellular myosin heavy chain-A exhibited high similarity in domains that allow binding of ATP and actin. The amino acid sequence of non-muscle myosin heavy chain-A from rat was 96% identical to that in human and 92% identical to that in chicken. Northern blot analysis of mRNA indicated the presence of single message of 7.4 kilobases. Northern blot, reverse-transcriptase polymerase chain reaction, and Western blot with isoform-specific antibodies indicated that RBL-2H3 cells expressed exclusively myosin heavy chain-A. Unlike rat PC12 cells, as well as a wide variety of other cultured cells and tissues, myosin heavy chain-B mRNA and protein were not detectable in RBL-2H3 cells. Because RBL-2H3 cells can be stimulated to release secretory granules as well as newly generated arachidonic acid and cytokines but lack myosin heavy chain-B, this cell line may provide a unique model to study the role of myosin heavy chain-A in cellular responses to antigen and other stimulants.
从分泌型大鼠肥大细胞系RBL-2H3细胞的cDNA克隆中推导得到了脊椎动物细胞肌球蛋白重链A的完整氨基酸序列(1961个氨基酸)。大鼠、人类和鸡的细胞肌球蛋白重链A在允许ATP和肌动蛋白结合的结构域中表现出高度相似性。大鼠非肌肉肌球蛋白重链A的氨基酸序列与人类的序列有96%的同一性,与鸡的序列有92%的同一性。mRNA的Northern印迹分析表明存在一条7.4千碱基的单一信使RNA。Northern印迹、逆转录聚合酶链反应以及用亚型特异性抗体进行的Western印迹表明,RBL-2H3细胞仅表达肌球蛋白重链A。与大鼠PC12细胞以及多种其他培养细胞和组织不同,在RBL-2H3细胞中未检测到肌球蛋白重链B的mRNA和蛋白质。由于RBL-2H3细胞可被刺激释放分泌颗粒以及新生成的花生四烯酸和细胞因子,但缺乏肌球蛋白重链B,该细胞系可能为研究肌球蛋白重链A在细胞对抗抗原和其他刺激物的反应中的作用提供一个独特的模型。