Myomerger induces fusion of non-fusogenic cells and is required for skeletal muscle development

Malgorzata E. Quinn, Qingnian Goh, Mitsutoshi Kurosaka, Dilani G. Gamage, Michael J. Petrany, Vikram Prasad and Douglas P. Millay ()
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Malgorzata E. Quinn: Cincinnati Children’s Hospital Medical Center
Qingnian Goh: Cincinnati Children’s Hospital Medical Center
Mitsutoshi Kurosaka: Cincinnati Children’s Hospital Medical Center
Dilani G. Gamage: Cincinnati Children’s Hospital Medical Center
Michael J. Petrany: Cincinnati Children’s Hospital Medical Center
Vikram Prasad: Cincinnati Children’s Hospital Medical Center
Douglas P. Millay: Cincinnati Children’s Hospital Medical Center

Nature Communications, 2017, vol. 8, issue 1, 1-9

Abstract: Abstract Despite the importance of cell fusion for mammalian development and physiology, the factors critical for this process remain to be fully defined, which has severely limited our ability to reconstitute cell fusion. Myomaker (Tmem8c) is a muscle-specific protein required for myoblast fusion. Expression of myomaker in fibroblasts drives their fusion with myoblasts, but not with other myomaker-expressing fibroblasts, highlighting the requirement of additional myoblast-derived factors for fusion. Here we show that Gm7325, which we name myomerger, induces the fusion of myomaker-expressing fibroblasts. Thus, myomaker and myomerger together confer fusogenic activity to otherwise non-fusogenic cells. Myomerger is skeletal muscle-specific and genetic deletion in mice results in a paucity of muscle fibres demonstrating its requirement for normal muscle formation. Myomerger deficient myocytes differentiate and harbour organized sarcomeres but are fusion-incompetent. Our findings identify myomerger as a fundamental myoblast fusion protein and establish a system that begins to reconstitute mammalian cell fusion.

Date: 2017
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DOI: 10.1038/ncomms15665

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