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首页> 外文期刊>Developmental biology >The MARVEL domain protein, Singles Bar, is required for progression past the pre-fusion complex stage of myoblast fusion
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The MARVEL domain protein, Singles Bar, is required for progression past the pre-fusion complex stage of myoblast fusion

机译:MARVEL结构域蛋白Singles Bar是成肌细胞融合前融合复杂阶段之后的进展所必需的

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摘要

Multinucleated myotubes develop by the sequential fusion of individual myoblasts. Using a convergence of genomic and classical genetic approaches, we have discovered a novel gene, singles bar (sing), that is essential for myoblast fusion. sing encodes a small multipass transmembrane protein containing a MARVEL domain, which is found in vertebrate proteins involved in processes such as tight junction formation and vesicle trafficking where-as in myoblast fusion-membrane apposition occurs. sing is expressed in both founder cells and fusion competent myoblasts, preceding and during myoblast fusion. Examination of embryos injected with double-stranded sing RNA or embryos homozygous for ethane methyl sulfonate-induced sing alleles revealed an identical phenotype: replacement of multinucleated myofibers by groups of single, myosin-expressing myoblasts at a stage when formation of the mature muscle pattern is complete in wild-type embryos. Unfused sing mutant myoblasts form clusters, suggesting that early recognition and adhesion of these cells are unimpaired. To further investigate this phenotype, we undertook electron microscopic ultrastructural studies of fusing myoblasts in both sing and wild-type embryos. These experiments revealed that more sing mutant myoblasts than wild-type contain pre-fusion complexes, which are characterized by electron-dense vesicles paired on either side of the fusing plasma membranes. In contrast, embryos mutant for another muscle fusion gene, blown fuse (blow), have a normal number of such complexes. Together, these results lead to the hypothesis that sing acts at a step distinct from that of blow, and that sing is required on both founder cell and fusion-competent myoblast membranes to allow progression past the pre-fusion complex stage of myoblast fusion, possibly by mediating fusion of the electron-dense vesicles to the plasma membrane. Published by Elsevier Inc.
机译:多核肌管通过单个成肌细胞的顺序融合而形成。使用基因组学和经典遗传学方法的融合,我们发现了一种新基因,单条杆(唱歌),这对于成肌细胞融合是必不可少的。 sing编码含有MARVEL结构域的小的多通道跨膜蛋白,该蛋白在参与紧密连接形成和囊泡运输等过程的脊椎动物蛋白中被发现,如成肌细胞融合膜并置。在成肌细胞融合之前和过程中,基础细胞和融合感受态成肌细胞均表达sing。检查注射双链sing RNA的胚胎或由乙烷甲基磺酸盐诱导的sing等位基因纯合的胚胎表现出相同的表型:在成熟肌肉模式形成的阶段,用表达肌动蛋白的单个成肌细胞组代替多核肌纤维在野生型胚胎中完整。未融合的单个突变体成肌细胞形成簇,表明这些细胞的早期识别和粘附没有受到损害。为了进一步研究这种表型,我们进行了电子显微超微结构研究,将单胚和野生型胚中的成肌细胞融合在一起。这些实验表明,与野生型相比,单种突变型成肌细胞中含有融合前复合物,其特征是在融合质膜的两侧配对有电子致密囊泡。相比之下,另一个肌肉融合基因突变的胚胎,即保险丝(blow),具有正常数量的这种复合物。总之,这些结果导致了这样一个假设:唱歌的作用不同于吹气,并且在基础细胞和具有融合能力的成肌细胞膜上都需要唱歌,以使进展超过成肌细胞融合的融合前复杂阶段。通过介导电子致密囊泡与质膜的融合。由Elsevier Inc.发布

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