A genetic screen for behavioral mutations that perturb dopaminergic homeostasis in mice

• Published in: Genes, brain and behavior Vol. 5; no. 1; pp. 19 - 28
• Main Authors: Speca, D. J., Rabbee, N., Chihara, D., Speed, T. P., Peterson, A. S.
• Format: Journal Article
• Language: English
• Published: Oxford, UK; Malden, USA Munksgaard International Publishers 01.02.2006
• Subjects: Animals; Chromosome Mapping; Dopamine; Dopamine - metabolism; Dopamine Plasma Membrane Transport Proteins - genetics; Dopamine Plasma Membrane Transport Proteins - metabolism; ENU; Ethylnitrosourea; Exploratory Behavior - physiology; Female; Genetic Carrier Screening; Genetic Testing; Homeostasis - genetics; Homozygote; Locomotor; Male; Mice; Mice, Inbred DBA; Mice, Knockout; Motor Activity - genetics; mouse; Mutagenesis - genetics; Mutagens; Phenotype; phenotype‐driven screen; Quantitative Trait Loci - genetics; Random Allocation
• ISSN: 1601-1848; 1601-183X
• DOI: 10.1111/j.1601-183X.2005.00127.x

Disruption of dopaminergic (DA) systems is thought to play a central role in the addictive process and in the pathophysiology of schizophrenia. Although inheritance plays an important role in the predisposition to these disorders, the genetic basis of this is not well understood. To provide additional insight, we have performed a modifier screen in mice designed to identify mutations that perturb DA homeostasis. With a genetic background sensitized by a mutation in the dopamine transporter (DAT), we used random chemical mutagenesis and screened for mutant mice with locomotor abnormalities. Four mutant lines were identified with quantitatively elevated levels of locomotor activity. Mapping of mutations in these lines identified two loci that alter activity only when dopamine levels are elevated by a DAT mutation and thus would only have been uncovered by this type of approach. One of these quantitative trait loci behaves as an enhancer of DA neurotransmission, whereas the other may act as a suppressor. In addition, we also identified three loci which are not dependent on the sensitized background but which also contribute to the overall locomotor phenotype.