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.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469413 | PMC |
http://dx.doi.org/10.1534/g3.118.200996 | DOI Listing |
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