Rno-miR-425-5p targets the DLST and SLC16A1 genes to reduce liver damage caused by excessive energy mobilization under cold stress

J Anim Physiol Anim Nutr (Berl). 2019 Jul;103(4):1251-1262. doi: 10.1111/jpn.13100. Epub 2019 May 14.

Abstract

MicroRNAs (miRNAs) are a class of single-stranded non-coding small RNA molecules, which participate in the regulation of many physiological processes, and play a crucial role in cancer, metabolism and other processes. Rno-miR-425-5p has been shown to play a role in the response to cold stress. To explore the mechanism by which rno-miR-425-5p regulates the response to cold stress, we analysed the candidate target genes of rno-miR-425-5p. After verification in rat hepatocyte BRL cells and in rat liver tissue, we identified several target genes that were altered in expression in response to cold stress. In rat liver tissue, the expression of rno-miR-425-5p was significantly increased and the expression levels of target genes DLST and SLC16A1 were decreased under cold stress. The miRNA and mRNA levels were analysed by quantitative real-time PCR and the protein levels were detected by Western blot analysis. Combined with the results of bioinformatic analysis, we concluded that rno-miR-425-5p reduced the expression of DLST and SLC16A1, inhibiting energy release from the tricarboxylic acid cycle and preventing the liver from being injured by excessive energy mobilization.

Keywords: DLST; SLC16A1 (MCT1); cold stress; miR-425.

MeSH terms

  • Acyltransferases / genetics
  • Acyltransferases / metabolism*
  • Animals
  • Cell Line
  • Cold Temperature*
  • Cold-Shock Response
  • Computational Biology
  • Energy Metabolism
  • Gene Expression Regulation
  • Hepatocytes / physiology
  • Laboratory Animal Science
  • Liver Diseases
  • Male
  • MicroRNAs / genetics*
  • Monocarboxylic Acid Transporters / genetics
  • Monocarboxylic Acid Transporters / metabolism*
  • Random Allocation
  • Rats
  • Specific Pathogen-Free Organisms
  • Stress, Physiological*
  • Symporters / genetics
  • Symporters / metabolism*

Substances

  • MicroRNAs
  • Monocarboxylic Acid Transporters
  • Symporters
  • monocarboxylate transport protein 1
  • Acyltransferases
  • dihydrolipoamide succinyltransferase