Genetics and differential expression of NADH:ubiquinone oxidoreductase B8 subunit in brains of genetic strains of mice differing in voluntary alcohol consumption

Biochim Biophys Acta. 2002 Dec 12;1579(2-3):164-72. doi: 10.1016/s0167-4781(02)00544-4.

Abstract

Inbred strains of mice remain a valuable resource for genetic dissection of complex traits including responses to drugs and chemicals, particularly alcohol. As a novel source of candidate genes for further analysis, we have used mRNA differential displays to identify genes with differential expression in the brains of ethanol-preferring (C57BL/6J) vs. ethanol-avoiding (A/J, BALB/c, and DBA/2J) strains, with and without ethanol i.p. treatments (4 g/kg). We report on one such gene, NADH:ubiquinone oxidoreductase B8 subunit, that has a higher expression in the C57BL/6J. Further, its expression also increases following ethanol treatment as compared to the three alcohol-avoiding strains. This regulatory feature follows three single nucleotide polymorphisms (SNPs) in the promoter region across the four strains studied. The four strains represent only two haplotypes, one C57BL/6J-specific and the other found in the three alcohol-avoiding strains. Interestingly, one of the observed SNPs (-687 A/G) is located in the putative TFIID binding site with potential to regulate the expression of this gene and contribute to genotype-specific alcohol responses and effects involving reactive oxygen species (ROS).

Publication types

  • Comparative Study

MeSH terms

  • Alcohol Drinking / genetics*
  • Alcohol Drinking / metabolism*
  • Animals
  • Base Sequence
  • Binding Sites
  • Brain / metabolism*
  • Electron Transport Complex I
  • Gene Expression Profiling
  • Gene Expression Regulation, Enzymologic
  • Mice
  • Mice, Inbred Strains
  • Molecular Sequence Data
  • NADH, NADPH Oxidoreductases / chemistry
  • NADH, NADPH Oxidoreductases / genetics*
  • NADH, NADPH Oxidoreductases / metabolism*
  • Polymorphism, Single Nucleotide
  • Promoter Regions, Genetic
  • RNA, Messenger / analysis
  • Sequence Alignment
  • Transcription Factor TFIID / metabolism

Substances

  • RNA, Messenger
  • Transcription Factor TFIID
  • NADH, NADPH Oxidoreductases
  • Electron Transport Complex I