Journal
ADDICTION BIOLOGY
Volume 16, Issue 3, Pages 499-509Publisher
WILEY
DOI: 10.1111/j.1369-1600.2011.00323.x
Keywords
alcohol dependence; CpG-SNPs; DNA methylation; epigenetics; prodynorphin; single-nucleotide polymorphisms
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Funding
- Swedish Council for Working Life and Social Research (FAS)
- Research Foundation of the Swedish Alcohol Retail Monopoly (SRA)
- AFA Fors kring
- Swedish Science Research Council
- University of Sydney
- National Health and Medical Research Council of Australia
- National Institute of Alcohol Abuse and Alcoholism
- NSW Department of Health
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The genetic, epigenetic and environmental factors may influence the risk for neuropsychiatric disease through their effects on gene transcription. Mechanistically, these effects may be integrated through regulation of methylation of CpG dinucleotides overlapping with single-nucleotide polymorphisms (SNPs) associated with a disorder. We addressed this hypothesis by analyzing methylation of prodynorphin (PDYN) CpG-SNPs associated with alcohol dependence, in human alcoholics. Postmortem specimens of the dorsolateral prefrontal cortex (dl-PFC) involved in cognitive control of addictive behavior were obtained from 14 alcohol-dependent and 14 control subjects. Methylation was measured by pyrosequencing after bisulfite treatment of DNA. DNA binding proteins were analyzed by electromobility shift assay. Three PDYN CpG-SNPs associated with alcoholism were found to be differently methylated in the human brain. In the dl-PFC of alcoholics, methylation levels of the C, non-risk variant of 3'-untranslated region (3'-UTR) SNP (rs2235749; C > T) were increased, and positively correlated with dynorphins. A DNA-binding factor that differentially targeted the T, risk allele and methylated and unmethylated C allele of this SNP was identified in the brain. The findings suggest a causal link between alcoholism-associated PDYN 3'-UTR CpG-SNP methylation, activation of PDYN transcription and vulnerability of individuals with the C, non-risk allele(s) to develop alcohol dependence.
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