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Volume 51 Issue 11
Nov.  2024
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Article Contents

Ectopic expression of Myomaker and Myomixer in slow muscle cells induces slow muscle fusion and myofiber death

doi: 10.1016/j.jgg.2024.08.006
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This work was supported by funding from the U.S. National Institute of Health (NIH) National Institute of Arthritis and Musculoskeletal and Skin Diseases (R01AR072703 to S.D.).

  • Received Date: 2024-05-31
  • Accepted Date: 2024-08-21
  • Rev Recd Date: 2024-08-21
  • Available Online: 2025-06-06
  • Publish Date: 2024-08-30
  • Zebrafish embryos possess two major types of myofibers, the slow and fast fibers, with distinct patterns of cell fusion. The fast muscle cells can fuse, while the slow muscle cells cannot. Here, we show that myomaker is expressed in both slow and fast muscle precursors, whereas myomixer is exclusive to fast muscle cells. The loss of Prdm1a, a regulator of slow muscle differentiation, results in strong myomaker and myomixer expression and slow muscle cell fusion. This abnormal fusion is further confirmed by the direct ectopic expression of myomaker or myomixer in slow muscle cells of transgenic models. Using the transgenic models, we show that the heterologous fusion between slow and fast muscle cells can alter slow muscle cell migration and gene expression. Furthermore, the overexpression of myomaker and myomixer also disrupts membrane integrity, resulting in muscle cell death. Collectively, this study identifies that the fiber-type-specific expression of fusogenic proteins is critical for preventing inappropriate fusion between slow and fast fibers in fish embryos, highlighting the need for precise regulation of fusogenic gene expression to maintain muscle fiber integrity and specificity.
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  • Barresi, M.J.F., D’Angelo, J.A., Hernandez, L.P., Devoto, S.H., 2001. Distinct mechanisms regulate slow-muscle development. Curr. Biol. 11, 1432-1438.
    Baxendale, S., Davison, C., Muxworthy, C., Wolff, C., Ingham, P.W., Roy, S., 2004. The B-cell maturation factor Blimp-1 specifies vertebrate slow-twitch muscle fiber identity in response to Hedgehog signaling. Nat. Genet. 36, 88-93.
    Bi, P., McAnally, J.R., Shelton, J.M., Sanchez-Ortiz, E., Bassel-Duby, R., Olson, E.N., 2018. Fusogenic micropeptide Myomixer is essential for satellite cell fusion and muscle regeneration. Proc. Natl. Acad. Sci. 115, 3864-3869.
    Bi, P., Ramirez-Martinez, A., Li, H., Cannavino, J., McAnally, J.R., Shelton, J.M., Sanchez-Ortiz, E., Bassel-Duby, R., Olson, E.N., 2017. Control of muscle formation by the fusogenic micropeptide myomixer. Science 356, 323-327.
    Billah, Md.M., Or Rashid, Md.M., Ahmed, M., Yamazaki, M., 2023. Antimicrobial peptide magainin 2-induced rupture of single giant unilamellar vesicles comprising E. coli polar lipids. Biochim. Biophys. Acta. BBA - Biomembr. 1865, 184112.
    Blau, H.M., Pavlath, G.K., Hardeman, E.C., Chiu, C.-P., Silberstein, L., Webster, S.G., Miller, S.C., Webster, C., 1985. Plasticity of the Differentiated State. Science 230, 758-766.
    Bryson-Richardson, R. j., Daggett, D. f., Cortes, F., Neyt, C., Keenan, D. g., Currie, P. d., 2005. Myosin heavy chain expression in zebrafish and slow muscle composition. Dev. Dyn. 233, 1018-1022.
    Chen, B., You, W., Wang, Y., Shan, T., 2020. The regulatory role of Myomaker and Myomixer-Myomerger-Minion in muscle development and regeneration. Cell. Mol. Life Sci. 77, 1551-1569.
    Chiu, C.-P., Blau, H.M., 1984. Reprogramming cell differentiation in the absence of DNA synthesis. Cell 37, 879-887.
    Devoto, S.H., Melancon, E., Eisen, J.S., Westerfield, M., 1996. Identification of separate slow and fast muscle precursor cells in vivo, prior to somite formation. Development 122, 3371-3380.
    Di Gioia, S.A., Connors, S., Matsunami, N., Cannavino, J., Rose, M.F., Gilette, N.M., Artoni, P., de Macena Sobreira, N.L., Chan, W.-M., Webb, B.D., et al., 2017. A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome. Nat. Commun. 8, 16077.
    Dunn, K., Vashisht, A., Hammond-Weinberger, D.R., 2022. Comparative in situ hybridization protocols in zebrafish. BioTechniques 73, 123-130.
    Elworthy, S., Hargrave, M., Knight, R., Mebus, K., Ingham, P.W., 2008. Expression of multiple slow myosin heavy chain genes reveals a diversity of zebrafish slow twitch muscle fibres with differing requirements for Hedgehog and Prdm1 activity. Development 135, 2115-2126.
    Gamage, D.G., Melikov, K., Munoz-Tello, P., Wherley, T.J., Focke, L.C., Leikina, E., Huffman, E., Diao, J., Kojetin, D.J., Prasad, V., et al., 2022. Phosphatidylserine orchestrates Myomerger membrane insertions to drive myoblast fusion. Proc. Natl. Acad. Sci. 119, e2202490119.
    Goh, Q., Millay, D.P., 2017. Requirement of myomaker-mediated stem cell fusion for skeletal muscle hypertrophy. eLife 6, e20007.
    Golani, G., Leikina, E., Melikov, K., Whitlock, J.M., Gamage, D.G., Luoma-Overstreet, G., Millay, D.P., Kozlov, M.M., Chernomordik, L.V., 2021. Myomerger promotes fusion pore by elastic coupling between proximal membrane leaflets and hemifusion diaphragm. Nat. Commun. 12, 495.
    Gurdon, J.B., Melton, D.A., 2008. Nuclear reprogramming in cells. Science 322, 1811-1815.
    Ham, T.J., Mapes, J., Kokel, D., Peterson, R.T., 2010. Live imaging of apoptotic cells in zebrafish. FASEB J. 24, 4336-4342.
    Hamer, P., McGeachie, J., Davies, M., Grounds, M., 2002. Evans blue dye as an in vivo marker of myofibre damage: optimising parameters for detecting initial myofibre membrane permeability. J. Anat. 200, 69-79.
    Henry, C.A., Amacher, S.L., 2004. Zebrafish slow muscle cell migration induces a wave of fast muscle morphogenesis. Dev. Cell 7, 917-923.
    Hernandez-Lagunas, L., Choi, I.F., Kaji, T., Simpson, P., Hershey, C., Zhou, Y., Zon, L., Mercola, M., Artinger, K.B., 2005. Zebrafish narrowminded disrupts the transcription factor prdm1 and is required for neural crest and sensory neuron specification. Dev. Biol. 278, 347-357.
    Hindi, S.M., Millay, D.P., 2022. All for one and one for all: regenerating skeletal muscle. Cold Spring Harb. Perspect. Biol. 14, a040824.
    Hromowyk, K.J., Talbot, J.C., Martin, B.L., Janssen, P.M.L., Amacher, S.L., 2020. Cell fusion is differentially regulated in zebrafish post-embryonic slow and fast muscle. Dev. Biol. 462, 85-100.
    Jackson, H.E., Ingham, P.W., 2013. Control of muscle fibre-type diversity during embryonic development: The zebrafish paradigm. Mech. Dev. 130, 447-457.
    Landemaine, A., Rescan, P.-Y., Gabillard, J.-C., 2014. Myomaker mediates fusion of fast myocytes in zebrafish embryos. Biochem. Biophys. Res. Commun. 451, 480-484.
    Lauter, G., Soll, I., Hauptmann, G., 2011. Two-color fluorescent in situ hybridization in the embryonic zebrafish brain using differential detection systems. BMC Dev. Biol. 11, 43.
    Lee, W., Lee, D.G., 2014. Magainin 2 induces bacterial cell death showing apoptotic properties. Curr. Microbiol. 69, 794-801.
    Leikina, E., Gamage, D.G., Prasad, V., Goykhberg, J., Crowe, M., Diao, J., Kozlov, M.M., Chernomordik, L.V., Millay, D.P., 2018. Myomaker and Myomerger work independently to control distinct steps of membrane remodeling during myoblast fusion. Dev. Cell 46, 767-780.e7.
    Li, M., Hromowyk, K.J., Amacher, S.L., Currie, P.D., 2017. Muscular dystrophy modeling in zebrafish, in: Methods in Cell Biology. Elsevier, pp. 347-380.
    Li, S., Wen, H., Du, S., 2020. Defective sarcomere organization and reduced larval locomotion and fish survival in slow muscle heavy chain 1 (smyhc1) mutants. FASEB J. 34, 1378-1397.
    Long, T., Zhang, Y., Donnelly, L., Li, H., Pien, Y.-C., Liu, N., Olson, E.N., Li, X., 2023. Cryo-EM structures of Myomaker reveal a molecular basis for myoblast fusion. Nat. Struct. Mol. Biol. 30, 1746-1754.
    Luo, Z., Shi, J., Pandey, P., Ruan, Z.-R., Sevdali, M., Bu, Y., Lu, Y., Du, S., Chen, E.H., 2022. The cellular architecture and molecular determinants of the zebrafish fusogenic synapse. Dev. Cell 57, 1582-1597.e6.
    Mendieta-Serrano, M.A., Dhar, S., Ng, B.H., Narayanan, R., Lee, J.J.Y., Ong, H.T., Toh, P.J.Y., Rollin, A., Roy, S., Saunders, T.E., 2022. Slow muscles guide fast myocyte fusion to ensure robust myotome formation despite the high spatiotemporal stochasticity of fusion events. Dev. Cell 57, 2095-2110.e5.
    Millay, D.P., 2022. Regulation of the myoblast fusion reaction for muscle development, regeneration, and adaptations. Exp. Cell Res. 415, 113134.
    Millay, D.P., Gamage, D.G., Quinn, M.E., Min, Y.-L., Mitani, Y., Bassel-Duby, R., Olson, E.N., 2016. Structure-function analysis of myomaker domains required for myoblast fusion. Proc. Natl. Acad. Sci. U. S. A. 113, 2116-2121.
    Millay, D.P., O’Rourke, J.R., Sutherland, L.B., Bezprozvannaya, S., Shelton, J.M., Bassel-Duby, R., Olson, E.N., 2013. Myomaker is a membrane activator of myoblast fusion and muscle formation. Nature 499, 301-305.
    Millay, D.P., Sutherland, L.B., Bassel-Duby, R., Olson, E.N., 2014. Myomaker is essential for muscle regeneration. Genes Dev. 28, 1641-1646.
    Mitani, Y., Vagnozzi, R.J., Millay, D.P., 2017. In vivo myomaker-mediated heterologous fusion and nuclear reprogramming. FASEB J. 31, 400-411.
    Morsch, M., Radford, R., Lee, A., Don, E.K., Badrock, A.P., Hall, T.E., Cole, N.J., Chung, R., 2015. In vivo characterization of microglial engulfment of dying neurons in the zebrafish spinal cord. Front. Cell. Neurosci. 9.
    Ono, Y., Yu, W., Jackson, H.E., Parkin, C.A., Ingham, P.W., 2015. Adaxial cell migration in the zebrafish embryo is an active cell autonomous property that requires the Prdm1a transcription factor. Differentiation 89, 77-86.
    Petrany, M.J., Millay, D.P., 2019. Cell fusion: merging membranes and making muscle. Trends Cell Biol. 29, 964-973.
    Petrany, M.J., Song, T., Sadayappan, S., Millay, D.P., 2020. Myocyte-derived Myomaker expression is required for regenerative fusion but exacerbates membrane instability in dystrophic myofibers. JCI Insight 5, e136095.
    Pomerantz, J.H., Mukherjee, S., Palermo, A.T., Blau, H.M., 2009. Reprogramming to a muscle fate by fusion recapitulates differentiation. J. Cell Sci. 122, 1045-1053.
    Powell, G.T., Wright, G.J., 2011. Jamb and Jamc are essential for vertebrate myocyte fusion. PLoS Biol. 9, e1001216.
    Quinn, M.E., Goh, Q., Kurosaka, M., Gamage, D.G., Petrany, M.J., Prasad, V., Millay, D.P., 2017. Myomerger induces fusion of non-fusogenic cells and is required for skeletal muscle development. Nat. Commun. 8, 15665.
    Ramirez-Martinez, A., Zhang, Y., van den Boogaard, M.-J., McAnally, J.R., Rodriguez-Caycedo, C., Chai, A.C., Chemello, F., Massink, M.P.G., Cuppen, I., Elferink, M.G., et al., 2022. Impaired activity of the fusogenic micropeptide Myomixer causes myopathy resembling Carey-Fineman-Ziter syndrome. J. Clin. Invest. 132, e159002.
    Roy, S., Wolff, C., Ingham, P.W., 2001. The u-boot mutation identifies a Hedgehog-regulated myogenic switch for fiber-type diversification in the zebrafish embryo. Genes Dev. 15, 1563-1576.
    Schneider, C.A., Rasband, W.S., Eliceiri, K.W., 2012. NIH Image to ImageJ: 25 years of image analysis. Nat. Methods 9, 671-675.
    Shi, J., Bi, P., Pei, J., Li, H., Grishin, N.V., Bassel-Duby, R., Chen, E.H., Olson, E.N., 2017. Requirement of the fusogenic micropeptide myomixer for muscle formation in zebrafish. Proc. Natl. Acad. Sci. U. S. A. 114, 11950-11955.
    Shi, J., Cai, M., Si, Y., Zhang, J., Du, S., 2018. Knockout of myomaker results in defective myoblast fusion, reduced muscle growth and increased adipocyte infiltration in zebrafish skeletal muscle. Hum. Mol. Genet. 27, 3542-3554.
    Smith, S.J., Horstick, E.J., Davidson, A.E., Dowling, J., 2015. Analysis of zebrafish larvae skeletal muscle integrity with evans blue dye. J. Vis. Exp. 53183.
    Srinivas, B.P., Woo, J., Leong, W.Y., Roy, S., 2007. A conserved molecular pathway mediates myoblast fusion in insects and vertebrates. Nat. Genet. 39, 781-786.
    Thisse, C., Thisse, B., 2008. High-resolution in situ hybridization to whole-mount zebrafish embryos. Nat. Protoc. 3, 59-69.
    Urasaki, A., Morvan, G., Kawakami, K., 2006. Functional dissection of the Tol2 transposable element identified the minimal cis-sequence and a highly repetitive sequence in the subterminal region essential for transposition. Genetics 174, 639-649.
    Witcher, P.C., Sun, C., Millay, D.P., 2023. Expression of Myomaker and Myomerger in myofibers causes muscle pathology. Skelet. Muscle 13, 8.
    Wu, P., Yong, P., Zhang, Z., Xu, R., Shang, R., Shi, J., Zhang, J., Bi, P., Chen, E., Du, S., 2022. Loss of myomixer results in defective myoblast fusion, impaired muscle growth, and severe myopathy in zebrafish. Mar. Biotechnol. 24, 1023-1038.
    Xing, L., Quist, T.S., Stevenson, T.J., Dahlem, T.J., Bonkowsky, J.L., 2014. Rapid and efficient zebrafish genotyping using PCR with high-resolution melt analysis. J. Vis. Exp. 5, e51138.
    Zaina, S., del Pilar Valencia-Morales, M., Tristan-Flores, F.E., Lund, G., 2013. Nuclear reprogramming and its role in vascular smooth muscle cells. Curr. Atheroscler. Rep. 15, 352.
    Zhang, H., Shang, R., Kim, K., Zheng, W., Johnson, C.J., Sun, L., Niu, X., Liu, Liang, Zhou, J., Liu, Lingshu, et al., 2022. Evolution of a chordate-specific mechanism for myoblast fusion. Sci. Adv. 8, eadd2696.
    Zhang, H., Wen, J., Bigot, A., Chen, J., Shang, R., Mouly, V., Bi, P., 2020. Human myotube formation is determined by MyoD-Myomixer/Myomaker axis. Sci. Adv. 6, eabc4062.
    Zhang, Q., Vashisht, A.A., O’Rourke, J., Corbel, S.Y., Moran, R., Romero, A., Miraglia, L., Zhang, J., Durrant, E., Schmedt, C., et al., 2017. The microprotein Minion controls cell fusion and muscle formation. Nat. Commun. 8, 15664.
    Zhang, W., Roy, S., 2017a. Myomaker is required for the fusion of fast-twitch myocytes in the zebrafish embryo. Dev. Biol. 423, 24-33.
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