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Neuropsychopharmacology. 2016 Dec;41(13):3025-3031. doi: 10.1038/npp.2016.113. Epub 2016 Jul 1.

Functional Impact of An ADHD-Associated DIRAS2 Promoter Polymorphism.

Author information

1
Department of Psychiatry, Psychosomatics and Psychotherapy, Translational Psychiatry, University Hospital Frankfurt, Frankfurt, Germany.
2
Department of Biomedicine, K.G. Jebsen Centre for Neuropsychiatric Disorders, University of Bergen, Bergen, Norway.
3
Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University of Würzburg, Würzburg, Germany.
4
Department of Translational Research in Psychiatry, Max Planck Institute of Psychiatry, Munich, Germany.
5
Department of Psychiatry, Psychosomatics and Psychotherapy, Molecular Psychiatry Laboratory of Translational Neuroscience, University of Würzburg, Würzburg, Germany.
6
Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA, USA.

Abstract

The DIRAS2 gene is coding for a small Ras GTPase with so far unknown function. In a previous study, we described the association of DIRAS2 rs1412005, as well as a haplotype containing this polymorphism and located in the promoter region of this gene with attention-deficit/hyperactivity disorder (ADHD). In the present study, we searched for rare variants within or near the DIRAS2 gene that might be associated with ADHD using next-generation sequencing. As we were not able to detect any rare variants associated with the disease, we sought to establish a functional role of DIRAS2 rs1412005 on the molecular or systems level. First, we investigated whether it has an influence on gene expression by means of a luciferase-based promoter assay. We could demonstrate that the minor risk allele goes along with the increased expression of the reporter gene. Next, we aimed to identify differences in response inhibition between risk-allele and non-risk allele carriers in children suffering from ADHD and healthy control individuals by analyzing event-related potentials in the electroencephalogram during a Go/NoGo task. Risk-allele carriers showed a changed NoGo anteriorization. Therefore, our results suggest an impact of the investigated polymorphism on the prefrontal response control in children with ADHD. These results imply that the promoter polymorphism is indeed the associated as well as in itself a causal variant. Further research is thus warranted to clarify the mechanisms linking DIRAS2 to ADHD.

PMID:
27364329
PMCID:
PMC5101550
DOI:
10.1038/npp.2016.113
[Indexed for MEDLINE]
Free PMC Article

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