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Vol. 298, Issue 2, 634-643, August 2001
Research Service, Veterans Affairs Medical Center (A.J., C.M.,
R.A.J., T.J.P., J.C.C., A.J.E., J.K.B.), Portland, Oregon; and
Department of Psychiatry (A.J., C.M., R.A.J.), Department of Behavioral
Neuroscience (A.J., C.L.C., T.J.P., J.C.C., J.K.B.), Department of
Physiology and Pharmacology (A.J., J.C.C., A.J.E.), and Portland
Alcohol Research Center (A.J., C.L.C., T.J.P., J.C.C., A.J.E., J.K.B.),
Oregon Health Sciences University, Portland, Oregon
Binding of 3
-(4-iodophenyl) tropane-2
-carboxylic acid methyl
ester ([125I]RTI-55) to the dopamine transporter (DAT) in
neostriatum from C57BL/6J, DBA/2J, and 21 BXD recombinant inbred (RI)
mouse strains indicated highly significant strain differences in DAT
density (Bmax) but no significant
differences in affinity (Kd) for this radioligand. Strain mean Bmax values and the
known genomic locations of 1390 marker loci were used to carry out a
genome-wide search for quantitative trait loci (QTLs), which are
chromosomal sites containing genes that influence DAT expression. This
search revealed an unusually large effect QTL on chromosome 19 in the region of the proopiomelanocortin pseudogene
Pomc-ps1 (8-11 cM), homologous to regions of human
chromosomes 9q21 and 11q12-13. This QTL (logarithm of the odds
4.7, df = 1, p = 3 × 10
6)
by conservative estimates accounts for just over half of the genetic
variation in DAT binding site density. The QTL is not the DAT gene
itself (Dat1, chromosome 13), but a powerful modulator of DAT expression in neostriatum. Furthermore, DAT expression levels in
20 of the BXD RI strains and the chromosome 19 QTL were correlated with
cocaine and methamphetamine-induced locomotor activation and thermic
responses (hypo- or hyperthermia), but were not correlated with
behaviors related to sensitization, reward, voluntary consumption,
stereotypy, or seizures induced by these two psychostimulant drugs. The
results suggest that there is a gene(s) on proximal chromosome 19 that
strongly influences DAT expression in neostriatum and may influence
psychostimulant-induced activity and thermal responses.
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