Differential epigenetic regulation of BDNF and NT-3 genes by trichostatin A and 5-aza-2'-deoxycytidine in Neuro-2a cells

Biochem Biophys Res Commun. 2010 Mar 26;394(1):173-7. doi: 10.1016/j.bbrc.2010.02.139. Epub 2010 Feb 25.

Abstract

To understand epigenetic regulation of neurotrophins in Neuro-2a mouse neuroblastoma cells, we investigated the alteration of CpG methylation of brain-derived neurotrophic factor (BDNF) promoter I and neurotrophin-3 (NT-3) promoter IB and that of histone modification in Neuro-2a cells. Bisulfite genomic sequencing showed that the CpG sites of BDNF promoter I were methylated in non-treated Neuro-2a cells and demethylated following 5-aza-2'-deoxycytidine (5-aza-dC) treatment. In contrast, methylation status of the NT-3 promoter IB did not change by 5-aza-dC treatment in Neuro-2a cells. Furthermore, we demonstrated that BDNF exon I-IX mRNA was induced by trichostatin A (TSA) treatment. However, NT-3 exon IB-II mRNA was not induced by TSA treatment. Chromatin immunoprecipitation assays showed that the levels of acetylated histones H3 and H4 on BDNF promoter I were increased by TSA. These results demonstrate that DNA methylation and/or histone modification regulate BDNF gene expression, but do not regulate NT-3 gene expression in Neuro-2a cells.

MeSH terms

  • Acetylation
  • Animals
  • Azacitidine / analogs & derivatives
  • Azacitidine / pharmacology
  • Brain-Derived Neurotrophic Factor / genetics*
  • Cell Line, Tumor
  • Chromatin Immunoprecipitation
  • CpG Islands
  • DNA Methylation*
  • DNA Modification Methylases / antagonists & inhibitors
  • Decitabine
  • Epigenesis, Genetic*
  • Exons / genetics
  • Histones / metabolism
  • Hydroxamic Acids / pharmacology
  • Mice
  • Nerve Growth Factors / genetics*
  • Neurons / drug effects
  • Neurons / metabolism*
  • Promoter Regions, Genetic

Substances

  • Brain-Derived Neurotrophic Factor
  • Histones
  • Hydroxamic Acids
  • Nerve Growth Factors
  • neurotropin 3, mouse
  • trichostatin A
  • Decitabine
  • DNA Modification Methylases
  • Azacitidine