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

Author

Listed:
  • 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)

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.

Suggested Citation

  • Malgorzata E. Quinn & Qingnian Goh & Mitsutoshi Kurosaka & Dilani G. Gamage & Michael J. Petrany & Vikram Prasad & Douglas P. Millay, 2017. "Myomerger induces fusion of non-fusogenic cells and is required for skeletal muscle development," Nature Communications, Nature, vol. 8(1), pages 1-9, August.
  • Handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms15665
    DOI: 10.1038/ncomms15665
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    Cited by:

    1. Viviane Tran & Sarah Nahlé & Amélie Robert & Inès Desanlis & Ryan Killoran & Sophie Ehresmann & Marie-Pier Thibault & David Barford & Kodi S. Ravichandran & Martin Sauvageau & Matthew J. Smith & Marie, 2022. "Biasing the conformation of ELMO2 reveals that myoblast fusion can be exploited to improve muscle regeneration," Nature Communications, Nature, vol. 13(1), pages 1-15, December.

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