Schultheis Dorothea, Schwirz Jonas, Frasch Manfred
Division of Developmental Biology, Department of Biology, Friedrich-Alexander University of Erlangen-Nürnberg (FAU), 91058 Erlangen, Germany.
Johann-Friedrich-Blumenbach-Institut, GZMB, Georg-August-Universität Göttingen, 37077, Göttingen, German.
G3 (Bethesda). 2019 Apr 9;9(4):1141-1151. doi: 10.1534/g3.118.200996.
In a large-scale RNAi screen in for genes with knock-down phenotypes in the larval somatic musculature, one recurring phenotype was the appearance of larval muscle fibers that were significantly thinner than those in control animals. Several of the genes producing this knock-down phenotype corresponded to orthologs of genes that are known to participate in myoblast fusion, particularly via their effects on actin polymerization. A new gene previously not implicated in myoblast fusion but displaying a similar thin-muscle knock-down phenotype was the ortholog of , which encodes an F-BAR and SH3 domain protein. Our genetic studies of and , a gene encoding a structurally related protein, in show that the encoded F-BAR proteins jointly contribute to efficient myoblast fusion during larval muscle development. Together with the F-Bar protein Syndapin they are also required for normal embryonic midgut morphogenesis. In addition, is required together with during the profound remodeling of the midgut visceral musculature during metamorphosis. We propose that these F-Bar proteins help govern proper morphogenesis particularly of the longitudinal midgut muscles during metamorphosis.
在一项针对幼虫体壁肌肉组织中具有敲低表型的基因进行的大规模RNA干扰筛选中,一种反复出现的表型是幼虫肌肉纤维明显比对照动物的更细。产生这种敲低表型的几个基因对应于已知参与成肌细胞融合的基因的直系同源物,特别是通过它们对肌动蛋白聚合的影响。一个以前未涉及成肌细胞融合但表现出类似细肌敲低表型的新基因是 的直系同源物,它编码一种F-BAR和SH3结构域蛋白。我们对 和 (一种编码结构相关蛋白的基因)在 中的基因研究表明,编码的F-BAR蛋白共同有助于幼虫肌肉发育过程中的有效成肌细胞融合。与F-Bar蛋白Syndapin一起,它们也是正常胚胎中肠形态发生所必需的。此外,在变态过程中中肠内脏肌肉组织的深刻重塑过程中, 与 一起是必需的。我们提出,这些F-Bar蛋白有助于特别是在变态过程中控制中肠纵肌的正常形态发生。