MicroRNA-21 Regulates PI3K/Akt/mTOR Signaling by Targeting TGFβI during Skeletal Muscle Development in Pigs

PLoS One. 2015 May 7;10(5):e0119396. doi: 10.1371/journal.pone.0119396. eCollection 2015.

Abstract

MicroRNAs (miRNAs), which are short (22-24 base pairs), non-coding RNAs, play critical roles in myogenesis. Using Solexa deep sequencing, we detected the expression levels of 229 and 209 miRNAs in swine skeletal muscle at 90 days post-coitus (E90) and 100 days postnatal (D100), respectively. A total of 138 miRNAs were up-regulated on E90, and 31 were up-regulated on D100. Of these, 9 miRNAs were selected for the validation of the small RNA libraries by quantitative RT-PCR (RT-qPCR). We found that miRNA-21 was down-regulated by 17-fold on D100 (P<0.001). Bioinformatics analysis suggested that the transforming growth factor beta-induced (TGFβI) gene was a potential target of miRNA-21. Both dual luciferase reporter assays and western blotting demonstrated that the TGFβI gene was regulated by miRNA-21. Co-expression analysis revealed that the mRNA expression levels of miRNA-21 and TGFβI were negatively correlated (r = -0.421, P = 0.026) in skeletal muscle during the 28 developmental stages. Our results revealed that more miRNAs are expressed in prenatal than in postnatal skeletal muscle. The miRNA-21 is a novel myogenic miRNA that is involved in skeletal muscle development and regulates PI3K/Akt/mTOR signaling by targeting the TGFβI gene.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Gene Expression Regulation, Developmental
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Molecular Sequence Data
  • Muscle, Skeletal / growth & development*
  • Muscle, Skeletal / metabolism
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Sequence Analysis, RNA
  • Signal Transduction
  • Swine
  • TOR Serine-Threonine Kinases / metabolism
  • Transforming Growth Factor beta / genetics*
  • Transforming Growth Factor beta / metabolism*

Substances

  • MicroRNAs
  • Transforming Growth Factor beta
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases

Associated data

  • SRA/SRP050975

Grants and funding

This study was supported by the National Natural Science Foundation of China (31171192, 31330074), the National Basic Research Program of China (2012CB124706-6), the National Key Project (2014ZX08009-001), and the Agricultural Science and Technology Innovation Program (ASTIP-IAS05). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.