Muscle-specific microRNA miR-206 promotes muscle differentiation

J Cell Biol. 2006 Aug 28;174(5):677-87. doi: 10.1083/jcb.200603008. Epub 2006 Aug 21.

Abstract

Three muscle-specific microRNAs, miR-206, -1, and -133, are induced during differentiation of C2C12 myoblasts in vitro. Transfection of miR-206 promotes differentiation despite the presence of serum, whereas inhibition of the microRNA by antisense oligonucleotide inhibits cell cycle withdrawal and differentiation, which are normally induced by serum deprivation. Among the many mRNAs that are down-regulated by miR-206, the p180 subunit of DNA polymerase alpha and three other genes are shown to be direct targets. Down-regulation of the polymerase inhibits DNA synthesis, an important component of the differentiation program. The direct targets are decreased by mRNA cleavage that is dependent on predicted microRNA target sites. Unlike small interfering RNA-directed cleavage, however, the 5' ends of the cleavage fragments are distributed and not confined to the target sites, suggesting involvement of exonucleases in the degradation process. In addition, inhibitors of myogenic transcription factors, Id1-3 and MyoR, are decreased upon miR-206 introduction, suggesting the presence of additional mechanisms by which microRNAs enforce the differentiation program.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors
  • Cell Differentiation*
  • Cell Line
  • Cell Proliferation
  • Connexin 43 / genetics
  • Connexin 43 / metabolism
  • DNA Polymerase I / genetics
  • DNA Polymerase I / metabolism
  • Down-Regulation
  • Lymphokines / genetics
  • Lymphokines / metabolism
  • Mice
  • MicroRNAs / biosynthesis
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Muscle Development
  • Myoblasts, Skeletal / cytology*
  • Myoblasts, Skeletal / metabolism
  • Oligonucleotide Array Sequence Analysis
  • Oligonucleotides, Antisense / genetics
  • Oligonucleotides, Antisense / metabolism
  • Proteins / genetics
  • Proteins / metabolism
  • RNA, Messenger / metabolism
  • Time Factors
  • Transcription Factors / metabolism*
  • Transfection

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Connexin 43
  • Hspc121 protein, mouse
  • Lymphokines
  • MicroRNAs
  • Msc protein, mouse
  • Oligonucleotides, Antisense
  • Proteins
  • RNA, Messenger
  • Transcription Factors
  • monocyte-macrophage differentiation factor
  • DNA Polymerase I