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A role for the Myoblast city homologues Dock1 and Dock5 and the adaptor proteins Crk and Crk-like in zebrafish myoblast fusion.

机译:在斑马鱼成肌细胞融合中,成肌细胞城市同源物Dock1和Dock5以及衔接蛋白Crk和Crk-like的作用。

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摘要

Myoblast fusion follows a defined sequence of events that is strikingly similar in vertebrates and invertebrates. Genetic analysis in Drosophila has identified many of the molecules that mediate the different steps in the fusion process; by contrast, the molecular basis of myoblast fusion during vertebrate embryogenesis remains poorly characterised. A key component of the intracellular fusion pathway in Drosophila is the protein encoded by the myoblast city (mbc) gene, a close homologue of the vertebrate protein dedicator of cytokinesis 1 (DOCK1, formerly DOCK180). Using morpholino antisense-oligonucleotide-mediated knockdown of gene activity in the zebrafish embryo, we show that the fusion of embryonic fast-twitch myoblasts requires the activities of Dock1 and the closely related Dock5 protein. In addition, we show that the adaptor proteins Crk and Crk-like (Crkl), with which Dock proteins are known to interact physically, are also required for myoblast fusion.
机译:成肌细胞融合遵循确定的事件序列,在脊椎动物和无脊椎动物中惊人地相似。果蝇的遗传分析已经鉴定出许多介导融合过程中不同步骤的分子。相比之下,在脊椎动物胚胎发生过程中成肌细胞融合的分子基础仍然很差。果蝇中细胞内融合途径的关键成分是成肌细胞城市(mbc)基因编码的蛋白质,成肌细胞城市(mbc)基因是胞质分裂1的脊椎动物蛋白质专用标记物(DOCK1,以前称为DOCK180)的紧密同源物。使用吗啉代反义寡核苷酸介导的斑马鱼胚胎基因活性的敲低,我们表明,胚胎快速抽搐成肌细胞的融合需要Dock1和密切相关的Dock5蛋白的活动。此外,我们表明成肌细胞融合还需要已知与Dock蛋白发生物理相互作用的衔接蛋白Crk和Crk-like(Crkl)。

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