MDM4 regulation by the let-7 miRNA family in the DNA damage response of glioma cells

FEBS Lett. 2015 Jul 8;589(15):1958-65. doi: 10.1016/j.febslet.2015.05.030. Epub 2015 May 27.

Abstract

Despite extensive investigation into the role of let-7 miRNAs in pathological tumor processes, their involvement in the DNA damage response remains unclear. Here we show that most let-7 family members down-regulate MDM4 expression via binding to MDM4 mRNA at a conserved DNA sequence. Expression of exogenous let-7 miRNA mimics decreased MDM4 protein but not mRNA levels. Several DNA damage reagents increased let-7 expression, thereby decreasing MDM4 protein levels in glioma cells. Inhibition of endogenous let-7 with antisense RNAs rescued MDM4 protein levels with or without MG132, a proteasome-dependent degradation inhibitor. An MDM4 mutation identified in a glioma patient was associated with loss of the putative MDM4 target site. Therefore, let-7 binding to MDM4 is implicated in the DNA damage response.

Keywords: Coding DNA sequence; DNA damage; Glioma; MDM4; MicroRNA let-7.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Brain Neoplasms / genetics*
  • Brain Neoplasms / metabolism
  • Brain Neoplasms / pathology
  • Cell Cycle Proteins
  • Cell Line, Tumor
  • DNA Damage*
  • Gene Expression Regulation, Neoplastic / physiology*
  • Glioma / genetics*
  • Glioma / metabolism
  • Glioma / pathology
  • Humans
  • MicroRNAs / physiology*
  • Mutation
  • Nuclear Proteins / genetics*
  • Proto-Oncogene Proteins / genetics*
  • Sequence Homology, Nucleic Acid

Substances

  • Cell Cycle Proteins
  • MDM4 protein, human
  • MicroRNAs
  • Nuclear Proteins
  • Proto-Oncogene Proteins
  • mirnlet7 microRNA, human