circHIPK3 regulates proliferation and differentiation of myoblast through the miR-7/TCF12 pathway

J Cell Physiol. 2021 Oct;236(10):6793-6805. doi: 10.1002/jcp.30363. Epub 2021 Mar 21.

Abstract

Skeletal muscle development is a complex biological process involving multiple key genes, signaling pathways and noncoding RNAs, including microRNAs and circular RNAs (circRNAs). However, the regulatory relationship among them is so complicated that it has not yet been fully elucidated. In this study, we found that miR-7 inhibited C2C12 cell proliferation and differentiation by targeting transcription factor 12 (TCF12). circHIPK3 acted as a competing endogenous RNA, and its overexpression effectively reversed the regulation of miR-7 on C2C12 cell proliferation and differentiation by increasing TCF12 expression. Taken together, our findings provide evidence that circHIPK3 regulates skeletal muscle development through the miR-7/TCF12 pathway. This study provides a scientific basis for further research on skeletal muscle development at the circRNA level.

Keywords: TCF12; circHIPK3; miR-7; myoblast proliferation and differentiation; skeletal muscle development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / metabolism*
  • Cell Differentiation*
  • Cell Line
  • Cell Proliferation*
  • Gene Expression Regulation
  • Mice
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Muscle Development*
  • Myoblasts, Skeletal / metabolism*
  • RNA, Circular / genetics
  • RNA, Circular / metabolism*
  • Signal Transduction

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • MIRN7 microRNA, mouse
  • MicroRNAs
  • RNA, Circular
  • Tcf12 protein, mouse