Contribution of Dopamine Transporter Gene Methylation Status to Cannabis Dependency.
Anna GrzywaczWojciech BarczakJolanta ChmielowiecKrzysztof ChmielowiecAleksandra SuchaneckaGrzegorz TrybekJolanta MasiakPawel JagielskiKatarzyna GrocholewiczBłażej RubiśPublished in: Brain sciences (2020)
The susceptibility to cannabis dependency results from the influence of numerous factors such as social, genetic, as well as epigenetic factors. Many studies have attempted to discover a molecular basis for this disease. However, our study aimed at evaluating the connection between altered methylation of the dopamine transporter gene (DAT1) promoter CpG sites and cannabis dependency. In the cases of some DNA sequences, including the DAT1 gene region, their methylation status in blood cells may reflect a systemic modulation in the whole organism. Consequently, we isolated the DNA from the peripheral blood cells from a group of 201 cannabis-dependent patients and 285 controls who were healthy volunteers and who were matched for age and sex. The DNA was subjected to bisulfite conversion and sequencing. Our analysis revealed no statistical differences in the general methylation status of the DAT1 gene promoter CpG island between the patients and controls. Yet, the analysis of individual CpG sites where methylation occurred indicated significant differences. These sites are known to be bound by transcription factors (e.g., SP1, p53, PAX5, or GR), which, apart from other functions, were shown to play a role in the development of the nervous system. Therefore, DAT1 gene promoter methylation studies may provide important insight into the mechanism of cannabis dependency.
Keyphrases
- dna methylation
- genome wide
- copy number
- gene expression
- end stage renal disease
- transcription factor
- newly diagnosed
- peripheral blood
- ejection fraction
- chronic kidney disease
- healthcare
- peritoneal dialysis
- prognostic factors
- oxidative stress
- cell free
- single molecule
- single cell
- mental health
- patient reported outcomes
- signaling pathway
- uric acid
- induced apoptosis
- cell death
- cell cycle arrest
- genome wide analysis