The dopamine D4 receptor (DRD4) is a member of the D2-like dopamine receptor family. Polymorphisms at the DRD4 gene have been examined for association with a wide range of neuropsychiatric disorders and normal behavioral variation. The DRD4 gene is unusual in its high amount of expressed polymorphis
Lack of imprinting of the human dopamine D4 receptor (DRD4) gene
✍ Scribed by Cichon, Sven; Nöthen, Markus M.; Wolf, Helmut K.; Propping, Peter
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 8 KB
- Volume
- 67
- Category
- Article
- ISSN
- 0148-7299
- DOI
- 10.1002/(sici)1096-8628(19960409)67:2<229::aid-ajmg17>3.0.co;2-l
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✦ Synopsis
The term genomic imprinting has been used to refer to the differential expression of genetic material depending on whether it has come from the male or female parent. In humans, the chromosomal region llp15.5 has been shown to contain 2 imprinted genes (H19 and IGF2). The gene for the dopamine D4 receptor (DRDU, which is of great interest for research into neuropsychiatric disorders and psychopharmacology, is also located in this area. In the present study, we have examined the imprinting status of the DRD4 gene in brain tissue of an epileptic patient who was heterozygous for a 12 bp repeat polymorphism in exon 1 of the DRD4 gene. W e show that both alleles are expressed in equivalent amounts. W e therefore conclude that the DRD4 gene is not imprinted in the human brain.
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