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Myomerger induces fusion of non-fusogenic cells and is required for skeletal muscle development.
- Source :
-
Nature communications [Nat Commun] 2017 Jun 01; Vol. 8, pp. 15665. Date of Electronic Publication: 2017 Jun 01. - Publication Year :
- 2017
-
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.
- Subjects :
- Animals
CRISPR-Cas Systems
Cell Communication
Cell Differentiation
Computational Biology
Female
Fibroblasts cytology
Male
Membrane Proteins genetics
Membrane Proteins metabolism
Mice
Mice, Inbred C57BL
Mice, Knockout
Myoblasts cytology
NIH 3T3 Cells
Oligonucleotide Array Sequence Analysis
Cell Fusion
Membrane Proteins physiology
Muscle Development
Muscle Fibers, Skeletal physiology
Muscle Proteins physiology
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 8
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 28569755
- Full Text :
- https://doi.org/10.1038/ncomms15665