Potassium bromate, a potent DNA oxidizing agent, exacerbates germline repeat expansion in a fragile X premutation mouse model

Hum Mutat. 2010 May;31(5):611-6. doi: 10.1002/humu.21237.

Abstract

Tandem repeat expansion is responsible for the Repeat Expansion Diseases, a group of human genetic disorders that includes Fragile X syndrome (FXS). FXS results from expansion of a premutation (PM) allele having 55-200 CGG.CCG-repeats in the 5' UTR of the FMR1 gene. The mechanism of expansion is unknown. We have treated FX PM mice with potassium bromate (KBrO(3)), a potent DNA oxidizing agent. We then monitored the germline and somatic expansion frequency in the progeny of these animals. We show here that KBrO(3) increased both the level of 8-oxoG in the oocytes of treated animals and the germline expansion frequency. Our data thus suggest that oxidative damage may be a factor that could affect expansion risk in humans.

Publication types

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

MeSH terms

  • 8-Hydroxy-2'-Deoxyguanosine
  • Animals
  • Bromates / pharmacology*
  • DNA Damage / drug effects
  • DNA Damage / genetics
  • Deoxyguanosine / analogs & derivatives
  • Deoxyguanosine / pharmacology
  • Disease Models, Animal
  • Flap Endonucleases / genetics
  • Fragile X Syndrome / genetics*
  • Humans
  • Mice
  • Mice, Knockout
  • Tandem Repeat Sequences
  • Trinucleotide Repeat Expansion / drug effects
  • Trinucleotide Repeat Expansion / genetics*

Substances

  • Bromates
  • potassium bromate
  • 8-Hydroxy-2'-Deoxyguanosine
  • Flap Endonucleases
  • Deoxyguanosine