miR-205 Regulates the Fusion of Porcine Myoblast by Targeting the Myomaker Gene

Cells. 2023 Apr 7;12(8):1107. doi: 10.3390/cells12081107.

Abstract

Skeletal muscle formation is an extremely important step in animal growth and development. Recent studies have found that TMEM8c (also known as Myomaker, MYMK), a muscle-specific transmembrane protein, can promote myoblast fusion and plays a key role in the normal development of skeletal muscle. However, the effect of Myomaker on porcine (Sus scrofa) myoblast fusion and the underlying regulatory mechanisms remain largely unknown. Therefore, in this study, we focused on the role and corresponding regulatory mechanism of the Myomaker gene during skeletal muscle development, cell differentiation, and muscle injury repair in pigs. We obtained the entire 3' UTR sequence of porcine Myomaker using the 3' RACE approach and found that miR-205 inhibited porcine myoblast fusion by targeting the 3' UTR of Myomaker. In addition, based on a constructed porcine acute muscle injury model, we discovered that both the mRNA and protein expression of Myomaker were activated in the injured muscle, while miR-205 expression was significantly inhibited during skeletal muscle regeneration. The negative regulatory relationship between miR-205 and Myomaker was further confirmed in vivo. Taken together, the present study reveals that Myomaker plays a role during porcine myoblast fusion and skeletal muscle regeneration and demonstrates that miR-205 inhibits myoblast fusion through targeted regulation of the expression of Myomaker.

Keywords: Myomaker; miR-205; muscle regeneration; myoblast fusion; pig.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions / genetics
  • Animals
  • Membrane Proteins / metabolism
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • Muscle, Skeletal / metabolism
  • Muscular Diseases* / genetics
  • Myoblasts / metabolism
  • Swine

Substances

  • 3' Untranslated Regions
  • Membrane Proteins
  • MicroRNAs

Grants and funding

This work was supported by grants from the National Key R & D Program of China (2020YFA0509500); the National Natural Science Foundation of China (U19A2036 and 32072687); the Major Science and Technology Projects of Tibet Autonomous Region (XZ202101ZD0005N); the Sichuan Science and Technology Program (2019YFN0035, 2021YFYZ0009 and 2021YFH0033); the Special Support for Postdoctoral Research Projects of Chongqing (2020379); the Municipal Financial Special Fund of Chongqing Academy of Animal Science (21518); the Performance Incentive Guidance for Scientific Research Institution of Chongqing (cstc2019jxj10039); and the China Agriculture Research System of MOF and MARA (CARS-35-01A).