Bute Medical School, University of St. Andrews, St. Andrews, Scotland, UK.
Am J Med Genet B Neuropsychiatr Genet. 2010 Sep;153B(6):1228-33. doi: 10.1002/ajmg.b.31084.
Genetic variation within the dopamine D4 receptor (DRD4) gene has been implicated in many neuropsychiatric disorders and behavioral traits. This variation includes the extensively studied exon 3 variably numbered tandem repeat (VNTR), and several 5' polymorphisms including a120-bp duplication and two single-nucleotide polymorphisms at -521 C/T (rs1800955) and -616 C/G (rs747302). Several reports have provided evidence for a functional role for some of these variants using in vitro techniques. This study investigated the functionality of these polymorphisms in 28 human post-mortem brain tissue samples by quantifying DRD4 mRNA expression in relation to genotype. No statistically significant relationship between genotype and mRNA expression levels was found for these four polymorphisms although a weak trend toward the 7-repeat of the exon 3 VNTR reducing DRD4 mRNA expression was found. Employing post-mortem brain tissue, rather than using in vitro techniques may provide a more relevant paradigm to study functional effects of reported risk alleles.
多巴胺 D4 受体(DRD4)基因内的遗传变异与许多神经精神疾病和行为特征有关。这种变异包括广泛研究的外显子 3 可变编号串联重复(VNTR),以及几个 5' 多态性,包括 120bp 重复和两个单核苷酸多态性 -521 C/T(rs1800955)和 -616 C/G(rs747302)。一些报告使用体外技术提供了这些变体具有功能作用的证据。本研究通过定量分析与基因型相关的 DRD4 mRNA 表达,在 28 个人死后脑组织样本中研究了这些多态性的功能。尽管发现 3' 外显子 VNTR 的 7 重复降低了 DRD4 mRNA 表达,但这四个多态性与 mRNA 表达水平之间没有统计学上显著的关系。使用死后脑组织而不是体外技术可能提供更相关的范例来研究报道的风险等位基因的功能影响。