| Literature DB >> 29078404 |
Jun Shi1,2, Pengpeng Bi1,2,3, Jimin Pei4, Hui Li1,2,3, Nick V Grishin4,5, Rhonda Bassel-Duby1,2,3, Elizabeth H Chen6,2, Eric N Olson6,2,3.
Abstract
Skeletal muscle formation requires fusion of mononucleated myoblasts to form multinucleated myofibers. The muscle-specific membrane proteins myomaker and myomixer cooperate to drive mammalian myoblast fusion. Whereas myomaker is highly conserved across diverse vertebrate species, myomixer is a micropeptide that shows relatively weak cross-species conservation. To explore the functional conservation of myomixer, we investigated the expression and function of the zebrafish myomixer ortholog. Here we show that myomixer expression during zebrafish embryogenesis coincides with myoblast fusion, and genetic deletion of myomixer using CRISPR/Cas9 mutagenesis abolishes myoblast fusion in vivo. We also identify myomixer orthologs in other species of fish and reptiles, which can cooperate with myomaker and substitute for the fusogenic activity of mammalian myomixer. Sequence comparison of these diverse myomixer orthologs reveals key amino acid residues and a minimal fusogenic peptide motif that is necessary for promoting cell-cell fusion with myomaker. Our findings highlight the evolutionary conservation of the myomaker-myomixer partnership and provide insights into the molecular basis of myoblast fusion. Published under the PNAS license.Entities:
Keywords: fusogenic; micropeptide; myogenesis; myomaker; zebrafish
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Year: 2017 PMID: 29078404 PMCID: PMC5692600 DOI: 10.1073/pnas.1715229114
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205