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PMID: 16082693 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Sequence variation in the 3'-untranslated region of the dopamine transporter gene and attention-deficit hyperactivity disorder (ADHD).

Feng Y, Wigg KG, Makkar R, Ickowicz A, Pathare T, Tannock R, Roberts W, Malone M, Kennedy JL, Schachar R, Barr CL

Abstract

The dopamine transporter gene (DAT1) has been reported to be associated with attention-deficit hyperactivity disorder (ADHD) in a number of studies [Cook et al. (1995): Am J Human Genet 56(4):9993-998; Gill et al. (1997): Mol Psychiatry 2(4):311-313; Waldman et al. (1998): Am J Human Genet 63(6):1767-1776; Barr et al. (2001): Biol Psychiatry 49(4):333-339; Curran et al. (2001): Mol Psychiatry 6(4):425-428; Chen et al. (2003): Mol Psychiatry 8(4):393-396]. Specifically, the 10-repeat allele of the 40-bp variable number of tandem repeats (VNTR) polymorphism located in the 3' untranslated region (UTR) of the gene has been found to be associated with ADHD. There is evidence from in vitro studies indicating that variability in the repeat number, and sequence variation in the 3'-UTR of the DAT1 gene may influence the level of the dopamine transporter protein [Fuke et al. (2001): Pharmacogenomics J 1(2):152-156; Miller and Madras (2002): Mol Psychiatry 7(1):44-55]. In this study, we investigated whether DNA variation in the DAT1 3'UTR contributed to ADHD by genotyping DNA variants around the VNTR region in a sample of 178 ADHD families. These included a MspI polymorphism (rs27072), a DraI DNA change (T/C) reported to influence DAT1 expression levels, and a BstUI polymorphism (rs3863145) in addition to the VNTR. We also screened the VNTR region by direct resequencing to determine if there was sequence variation within the repeat units that could account for the association. Our results indicate that DAT1 is associated with ADHD in our sample but not with alleles of the VNTR polymorphism. We did not find any variation in the sequence for either the 10- or 9-repeat alleles in the probands screened nor did we observe the reported DraI (T/C) variation. Our results therefore refute the possibility of the reported DraI variation or alleles of the VNTR as the functional variants contributing to the disorder.

MeSH Terms
3' Untranslated Regions Animals Attention Deficit Disorder with Hyperactivity/genetics Base Sequence Deoxyribonucleases, Type II Site-Specific/genetics Dopamine Plasma Membrane Transport Proteins/genetics Genetic Variation Haplotypes Humans Mice Minisatellite Repeats Molecular Sequence Data
Chemicals
3' Untranslated Regions Dopamine Plasma Membrane Transport Proteins SLC6A3 protein, human Deoxyribonucleases, Type II Site-Specific TTTAAA -specific type II deoxyribonucleases
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Feng Yu
Cell and Molecular Biology Division, Toronto Western Research Institute, University Health Network, Toronto, Ontario, Canada.
Wigg Karen G
Makkar Rohit
Ickowicz Abel
Pathare Tejaswee
Tannock Rosemary
Roberts Wendy
Malone Molly
Kennedy James L
Schachar Russell
Barr Cathy L
Article Info
Journal
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
Abbr.
Am J Med Genet B Neuropsychiatr Genet
ISSN
1552-4841
Published
2005-11-05
Pages
1-6
Language
English
Region
United States
NLM ID
101235742
Subset
IM
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