Promoter methylation represses AT2R gene and increases brain hypoxic-ischemic injury in neonatal rats

Neurobiol Dis. 2013 Dec:60:32-8. doi: 10.1016/j.nbd.2013.08.011. Epub 2013 Aug 24.

Abstract

Perinatal nicotine exposure downregulated angiotensin II type 2 receptor (AT2R) in the developing brain and increased brain vulnerability to hypoxic-ischemic injury in male neonatal rats. We tested the hypothesis that site-specific CpG methylation at AT2R gene promoter contributes to the increased vulnerability of brain injury in the neonate. Nicotine was administered to pregnant rats from day 4 of gestation to day 10 after birth. Brain hypoxic-ischemic injury was induced in day 10 male pups. CpG methylation at AT2R promoter was determined in the brain by quantitative methylation-specific PCR. Nicotine exposure significantly increased the methylation of a single CpG-52 locus near the TATA-box at AT2R promoter. Electrophoretic mobility shift assay indicated that the methylation of CpG-52 significantly decreased the binding affinity of TATA-binding protein (TBP). Chromatin immunoprecipitation assay further demonstrated an increase in the binding of a methyl-binding protein and a decrease in TBP binding to AT2R promoter in vivo in neonatal brains of nicotine-treated animals. This resulted in AT2R gene repression in the brain. Intracerebroventricular administration of a demethylating agent 5-aza-2'-deoxycytidine abrogated the enhanced methylation of CpG-52, rescued the TBP binding, and restored AT2R gene expression. Of importance, 5-aza-2'-deoxycytidine reversed the nicotine-increased vulnerability of brain hypoxic-ischemic injury in the neonate. The finding provides mechanistic evidence of increased promoter methylation and resultant AT2R gene repression in the developing brain linking perinatal stress and a pathophysiological consequence of heightened vulnerability of brain hypoxic-ischemic encephalopathy in the neonate.

Keywords: AT(2)R; Hypoxic–ischemic encephalopathy; Methylation; Nicotine.

Publication types

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

MeSH terms

  • Animals
  • Animals, Newborn
  • Brain / drug effects
  • Brain / pathology
  • CpG Islands*
  • DNA Methylation*
  • Female
  • Hypoxia-Ischemia, Brain / genetics*
  • Hypoxia-Ischemia, Brain / pathology
  • Male
  • Nicotine / toxicity
  • Pregnancy
  • Prenatal Exposure Delayed Effects
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, Angiotensin, Type 2 / genetics*
  • Receptor, Angiotensin, Type 2 / metabolism
  • TATA Box*
  • TATA-Box Binding Protein / metabolism

Substances

  • Receptor, Angiotensin, Type 2
  • TATA-Box Binding Protein
  • Nicotine