Abstract
Human dopaminergic neurons are involved in the control of hormone secretion, voluntary movement, and emotional behavior. Mediating these effects are the dopamine D1 and D2 receptors. These macromolecules belong to a large family of related sequences known as the G protein-coupled receptors. The D2 receptors have been of special interest because they bind, with high affinity and specificity, many of the commonly prescribed antipsychotic drugs. We previously isolated a full-length cDNA clone of the rat D2 receptor. When a chromosome mapping panel was probed with the rat D2 receptor cDNA a 15-kb EcoRI restriction fragment was identified and localized to human chromosome 11. The rat cDNA was also used to clone a human genomic fragment, lambda hD2G1, which contains the last coding exon of the D2 receptor gene (DRD2) and 16.5 kb of 3' flanking sequence. Hybridization of lambda hD2G1 to a chromosome 11 regional mapping panel localized DRD2 to 11q. In situ hybridization of lambda hD2G1 to metaphase chromosomes refined this assignment to the q22-q23 junction of chromosome 11. A search for RFLPs associated with D2DR identified a frequent two-allele TaqI RFLP.
MeSH Terms
Chromosome Mapping
Chromosomes, Human, Pair 11
Cloning, Molecular
Deoxyribonucleases, Type II Site-Specific
Humans
Nucleic Acid Hybridization
Polymorphism, Restriction Fragment Length
Receptors, Dopamine/genetics
Receptors, Dopamine D2
Chemicals
Receptors, Dopamine
Receptors, Dopamine D2
Deoxyribonucleases, Type II Site-Specific
TCGA-specific type II deoxyribonucleases
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Grandy D K
Vollum Institute for Advanced Biomedical Research, Oregon Health Sciences University, Portland, 97201.
Litt M
Allen L
Bunzow J R
Marchionni M
Makam H
Reed L
Magenis R E
Civelli O
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