A Zfp609 circular RNA regulates myoblast differentiation by sponging miR-194-5p

Int J Biol Macromol. 2019 Jan:121:1308-1313. doi: 10.1016/j.ijbiomac.2018.09.039. Epub 2018 Sep 7.

Abstract

Skeletal muscle development and growth regulatory mechanism is the focus of both animal genetics and medicine. The recent studies indicate that covalently closed circular RNAs (circRNAs) also play important role on muscle development through sequestering specific miRNAs. The present study was conducted to determine the functional roles of circZfp609, a recently identified circRNA, in the regulation of myogenesis in mouse myoblast cell line (C2C12). circZfp609 is predicted to has binding sites of miR-194-5p. circZfp609 knockdown increased the expression of Myf5 and MyoG, which indicated that circZfp609 suppressed myogenic differentiation. Via a luciferase screening assay, circZfp609 is observed to sponge to miR-194-5p with four potential binding sites. Specifically, we show that circZfp609 can sponge miR-194-5p to sequester its inhibition on BCLAF1 so as to repress the myogenic differentiation. Modulation of circZfp609 expression in muscle tissue may emerge as a potential target in breeding strategies attempting to control muscle development.

Keywords: BCLAF1; Differentiation; Muscle; circRNA; miR-194.

MeSH terms

  • Animals
  • Base Sequence
  • Cell Differentiation / genetics*
  • Cell Line
  • Female
  • Gene Knockdown Techniques
  • HEK293 Cells
  • Humans
  • Mice
  • MicroRNAs / genetics*
  • Myoblasts / cytology*
  • RNA / genetics*
  • RNA, Circular
  • Trans-Activators / deficiency
  • Trans-Activators / genetics*

Substances

  • MIRN194 microRNA, mouse
  • MicroRNAs
  • RNA, Circular
  • Trans-Activators
  • Zfp609 protein, mouse
  • RNA