Developmental Dieldrin Exposure Alters DNA Methylation at Genes Related to Dopaminergic Neuron Development and Parkinson's Disease in Mouse Midbrain

Toxicol Sci. 2019 Jun 1;169(2):593-607. doi: 10.1093/toxsci/kfz069.

Abstract

Human and animal studies have shown that exposure to the organochlorine pesticide dieldrin is associated with increased risk of Parkinson's disease (PD). Despite previous work showing a link between developmental dieldrin exposure and increased neuronal susceptibility to MPTP toxicity in male C57BL/6 mice, the mechanism mediating this effect has not been identified. Here, we tested the hypothesis that developmental exposure to dieldrin increases neuronal susceptibility via genome-wide changes in DNA methylation. Starting at 8 weeks of age and prior to mating, female C57BL/6 mice were exposed to 0.3 mg/kg dieldrin by feeding (every 3 days) throughout breeding, gestation, and lactation. At 12 weeks of age, pups were sacrificed and ventral mesencephalon, containing primarily substantia nigra, was microdissected. DNA was isolated and dieldrin-related changes in DNA methylation were assessed via reduced representation bisulfite sequencing. We identified significant, sex-specific differentially methylated CpGs (DMCs) and regions (DMRs) by developmental dieldrin exposure (false discovery rate < 0.05), including DMCs at the Nr4a2 and Lmx1b genes, which are involved in dopaminergic neuron development and maintenance. Developmental dieldrin exposure had distinct effects on the male and female epigenome. Together, our data suggest that developmental dieldrin exposure establishes sex-specific poised epigenetic states early in life. These poised epigenomes may mediate sensitivity to subsequent toxic stimuli and contribute to the development of late-life neurodegenerative disease, including PD.

Keywords: DNA methylation; Parkinson’s disease; RNA-sequencing; dieldrin; epigenetics; pesticides.

Publication types

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

MeSH terms

  • Animals
  • DNA Methylation / drug effects*
  • Dieldrin / toxicity*
  • Dopaminergic Neurons / drug effects*
  • Dopaminergic Neurons / physiology
  • Female
  • Fetus / drug effects*
  • GRB10 Adaptor Protein / genetics
  • Male
  • Mesencephalon / drug effects*
  • Mesencephalon / metabolism
  • Mice, Inbred C57BL
  • Parkinson Disease / etiology*
  • Sex Characteristics

Substances

  • Grb10 protein, mouse
  • GRB10 Adaptor Protein
  • Dieldrin