Energizing miRNA research: a review of the role of miRNAs in lipid metabolism, with a prediction that miR-103/107 regulates human metabolic pathways

Mol Genet Metab. 2007 Jul;91(3):209-17. doi: 10.1016/j.ymgme.2007.03.011. Epub 2007 May 22.

Abstract

MicroRNAs (miRNAs) are powerful regulators of gene expression. Although first discovered in worm larvae, miRNAs play fundamental biological roles-including in humans-well beyond development. MiRNAs participate in the regulation of metabolism (including lipid metabolism) for all animal species studied. A review of the fascinating and fast-growing literature on miRNA regulation of metabolism can be parsed into three main categories: (1) adipocyte biochemistry and cell fate determination; (2) regulation of metabolic biochemistry in invertebrates; and (3) regulation of metabolic biochemistry in mammals. Most research into the 'function' of a given miRNA in metabolic pathways has concentrated on a given miRNA acting upon a particular 'target' mRNA. Whereas in some biological contexts the effects of a given miRNA:mRNA pair may predominate, this might not be the case generally. In order to provide an example of how a single miRNA could regulate multiple 'target' mRNAs or even entire human metabolic pathways, we include a discussion of metabolic pathways that are predicted to be regulated by the miRNA paralogs, miR-103 and miR-107. These miRNAs, which exist in vertebrate genomes within introns of the pantothenate kinase (PANK) genes, are predicted by bioinformatics to affect multiple mRNA targets in pathways that involve cellular Acetyl-CoA and lipid levels. Significantly, PANK enzymes also affect these pathways, so the miRNA and 'host' gene may act synergistically. These predictions require experimental verification. In conclusion, a review of the literature on miRNA regulation of metabolism leads us believe that the future will provide researchers with many additional energizing revelations.

Publication types

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

MeSH terms

  • Acetyl Coenzyme A / metabolism
  • Adipocytes / physiology
  • Animals
  • Cells, Cultured
  • Energy Metabolism
  • Enzyme Activation
  • Humans
  • Lipid Metabolism*
  • Metabolic Networks and Pathways*
  • MicroRNAs / physiology*
  • Phosphotransferases (Alcohol Group Acceptor) / metabolism*
  • RNA, Messenger / metabolism
  • Ribosomes / metabolism

Substances

  • MicroRNAs
  • RNA, Messenger
  • Acetyl Coenzyme A
  • Phosphotransferases (Alcohol Group Acceptor)
  • pantothenate kinase