Methylation by NSun2 represses the levels and function of microRNA 125b

Mol Cell Biol. 2014 Oct 1;34(19):3630-41. doi: 10.1128/MCB.00243-14. Epub 2014 Jul 21.

Abstract

Methylation is a prevalent posttranscriptional modification of RNAs. However, whether mammalian microRNAs are methylated is unknown. Here, we show that the tRNA methyltransferase NSun2 methylates primary (pri-miR-125b), precursor (pre-miR-125b), and mature microRNA 125b (miR-125b) in vitro and in vivo. Methylation by NSun2 inhibits the processing of pri-miR-125b2 into pre-miR-125b2, decreases the cleavage of pre-miR-125b2 into miR-125, and attenuates the recruitment of RISC by miR-125, thereby repressing the function of miR-125b in silencing gene expression. Our results highlight the impact of miR-125b function via methylation by NSun2.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carboxypeptidases / metabolism
  • DNA Methylation*
  • Epigenesis, Genetic
  • Gene Silencing
  • HeLa Cells
  • Humans
  • Hydrogen Peroxide / pharmacology
  • Methyltransferases / genetics*
  • MicroRNAs / metabolism*
  • Oxidative Stress
  • RNA Processing, Post-Transcriptional
  • RNA, Messenger / genetics

Substances

  • MIRN125 microRNA, human
  • MicroRNAs
  • RNA, Messenger
  • Hydrogen Peroxide
  • Methyltransferases
  • NSUN2 protein, human
  • Carboxypeptidases
  • SCPEP1 protein, human