Alignment of the transcriptome with individual variation in animals selectively bred for High Drinking-In-the-Dark (HDID)

Alcohol. 2017 May:60:115-120. doi: 10.1016/j.alcohol.2017.02.176. Epub 2017 Apr 12.

Abstract

Among animals at risk for excessive ethanol consumption such as the HDID selected mouse lines, there is considerable individual variation in the amount of ethanol consumed and the associated blood ethanol concentrations (BECs). For the HDID lines, this variation occurs even though the residual genetic variation associated with the DID phenotype has been largely exhausted and thus is most likely associated with epigenetic factors. Here we focus on the question of whether the genes associated with individual variation in HDID-1 mice are different from those associated with selection (risk) (Iancu et al., 2013). Thirty-three HDID-1 mice were phenotyped for their BECs at the end of a standard DID trial, were sacrificed 3 weeks later, and RNA-Seq was used to analyze the striatal transcriptome. The data obtained illustrate that there is considerable overlap of the risk and variation gene sets, both focused on the fine-tuning of synaptic plasticity.

Keywords: Excessive ethanol consumption; Individual variation; Risk.

Publication types

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

MeSH terms

  • Alcohol Drinking / adverse effects
  • Alcohol Drinking / blood
  • Alcohol Drinking / genetics*
  • Alcohol Drinking / psychology
  • Animals
  • Behavior, Animal / drug effects*
  • Blood Alcohol Content
  • Brain / drug effects*
  • Brain / metabolism
  • Brain / physiopathology
  • Darkness*
  • Epigenesis, Genetic / drug effects
  • Ethanol / blood
  • Ethanol / toxicity*
  • Female
  • Gene Expression Profiling / methods
  • Genetic Variation*
  • Genotype
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Models, Animal
  • N-Methylaspartate / metabolism
  • Neuronal Plasticity / drug effects
  • Neuronal Plasticity / genetics
  • Phenotype
  • Synaptic Transmission / drug effects
  • Synaptic Transmission / genetics
  • Transcriptome / drug effects*

Substances

  • Blood Alcohol Content
  • Ethanol
  • N-Methylaspartate