Human Molecular Genetics, Vol 6, 577-582, Copyright © 1997 by Oxford University Press
T Arinami, M Gao, H Hamaguchi and M Toru
An excess dopaminergic activity may be implicated in the etiology of
schizophrenia. Our objective was to identify nucleotide variants in the 5'
region of the dopamine D2 receptor gene (DRD2) and to clarify their effects
on schizophrenia. We identified two polymorphisms, the A-241G and -141C
Ins/Del, by examination of 259 bp in the 5'-flanking region and 249 bp of
exon 1 of DRD2. Reporter constructs containing the -141C Del allele cloned
into a luciferase reporter plasmid drove 21% (Y-79 cells) and 43% (293
cells) expression compared with the -141C Ins allele. In a case-control
study, the -141C Del allele frequency was significantly lower in 260
schizophrenic patients than in 312 controls (OR = 0.60, 95%CI 0.44-0.81, P
< 0.001). No significant association was found between the A-241G
polymorphism and in vitro luciferase activity, or in allele frequency
between the patients versus controls. These findings show that the -141C
Ins/Del may be a functional polymorphism in the 5'-promoter region of DRD2
and may affect the susceptibility to schizophrenia.
ARTICLES
A functional polymorphism in the promoter region of the dopamine D2 receptor gene is associated with schizophrenia
Department of Medical Genetics, Institute of Basic Medical Sciences, University of Tsukuba, Japan.
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