The VNTR polymorphism in the human dopamine transporter gene: improved detection and absence of association of VNTR alleles with attention-deficit hyperactivity disorder.
Author: Simsek M, Al Sharbati M, Al Adawi S, Lawatia K
Source:
Genetic Testing, 10(1), 31-34.
The human dopamine transporter (DAT1) gene contains a variable number tandem
repeat (VNTR) in its 3'-untranslated region because of repetition of a 40-bp core
sequence. Methods available for the diagnosis of this polymorphism are limited in
number. We have developed a new polymerase chain reaction (PCR) test, which is
similar to that described originally by Vandenbergh's group, but provides a
better detection of the VNTR alleles in the human DAT1 gene. Using two
independent PCR methods, we have determined the distribution of VNTR alleles in
110 healthy Omani subjects, and in 92 children with attention-deficit
hyperactivity disorder (ADHD). The frequency of the risk allele (DAT1*10) was
similar in the healthy subjects and ADHD cases, indicating absence of association
of this allele with ADHD in Oman.