TY - JOUR
T1 - Trout myomaker contains 14 minisatellites and two sequence extensions but retains fusogenic function
AU - Landemaine, Aurélie
AU - Ramirez-Martinez, Andres
AU - Monestier, Olivier
AU - Sabin, Nathalie
AU - Rescan, Pierre Yves
AU - Olson, Eric N.
AU - Gabillard, Jean Charles
N1 - Funding Information:
This work was supported by National Institutes of Health Grants AR-067294, HL-130253, DK-099653, and HD-087351. This study was also supported by French National Research Agency Grant ANR-12-JSV7–0001-01, by Brit-tany region funds (to A. L.), and by Robert A. Welch Foundation Grant 1-0025 (to E. N. O.). The authors declare that they have no conflicts of inter-est with the contents of this article. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Publisher Copyright:
© 2019 Landemaine et al. Published under exclusive license by The American Society for Biochemistry and Molecular Biology, Inc.
PY - 2019/4/19
Y1 - 2019/4/19
N2 - The formation of new myofibers in vertebrates occurs by myoblast fusion and requires fusogenic activity of the muscle-specific membrane protein myomaker. Here, using in silico (BLAST) genome analyses, we show that the myomaker gene from trout includes 14 minisatellites, indicating that it has an unusual structure compared with those of other animal species. We found that the trout myomaker gene encodes a 434 –amino acid (aa) protein, in accordance with its apparent molecular mass (40 kDa) observed by immunoblotting. The first half of the trout myomaker protein (1–220 aa) is similar to the 221-aa mouse myomaker protein, whereas the second half (222–234 aa) does not correspond to any known motifs and arises from two protein extensions. The first extension (70 aa) apparently appeared with the radiation of the bony fish clade Euteleostei, whereas the second extension (up to 236 aa) is restricted to the superorder Protacanthopterygii (containing salmonids and pike) and corresponds to the insertion of minisatellites having a length of 30 nucleotides. According to gene expression analyses, trout myomaker expression is consistently associated with the formation of new myofibers during embryonic development, postlarval growth, and muscle regeneration. Using cell-mixing experiments, we observed that trout myomaker has retained the ability to drive the fusion of mouse fibroblasts with C2C12 myoblasts. Our work reveals that trout myomaker has fusogenic function despite containing two protein extensions.
AB - The formation of new myofibers in vertebrates occurs by myoblast fusion and requires fusogenic activity of the muscle-specific membrane protein myomaker. Here, using in silico (BLAST) genome analyses, we show that the myomaker gene from trout includes 14 minisatellites, indicating that it has an unusual structure compared with those of other animal species. We found that the trout myomaker gene encodes a 434 –amino acid (aa) protein, in accordance with its apparent molecular mass (40 kDa) observed by immunoblotting. The first half of the trout myomaker protein (1–220 aa) is similar to the 221-aa mouse myomaker protein, whereas the second half (222–234 aa) does not correspond to any known motifs and arises from two protein extensions. The first extension (70 aa) apparently appeared with the radiation of the bony fish clade Euteleostei, whereas the second extension (up to 236 aa) is restricted to the superorder Protacanthopterygii (containing salmonids and pike) and corresponds to the insertion of minisatellites having a length of 30 nucleotides. According to gene expression analyses, trout myomaker expression is consistently associated with the formation of new myofibers during embryonic development, postlarval growth, and muscle regeneration. Using cell-mixing experiments, we observed that trout myomaker has retained the ability to drive the fusion of mouse fibroblasts with C2C12 myoblasts. Our work reveals that trout myomaker has fusogenic function despite containing two protein extensions.
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U2 - 10.1074/jbc.RA118.006047
DO - 10.1074/jbc.RA118.006047
M3 - Article
C2 - 30819805
AN - SCOPUS:85064815808
SN - 0021-9258
VL - 294
SP - 6364
EP - 6374
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 16
ER -