D'Souza Ursula M, Russ Carsten, Tahir Eda, Mill Jonathan, McGuffin Peter, Asherson Philip J, Craig Ian W
Medical Research Council Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, King's College London, Box Number P082, Denmark Hill, London SE5 8AF, United Kingdom.
Biol Psychiatry. 2004 Nov 1;56(9):691-7. doi: 10.1016/j.biopsych.2004.08.008.
Several polymorphisms have been identified in the 5'flanking region of the human dopamine D(4) receptor gene (DRD4), including a tandem duplication polymorphism. This comprises a 120-base-pair repeat sequence that is known to have different allele frequencies in various populations around the world. Furthermore, various studies have revealed evidence of linkage to attention-deficit/hyperactivity disorder and association with schizophrenia and methamphetamine abuse. The location of the polymorphism in the 5'regulatory region of the DRD4 gene and the fact that it consists of potential transcription factor binding sites suggest that it might confer differential transcriptional activity of the alleles.
We investigated the functional effects of this gene variant with transient transfection methods in four human cell lines and then assessed transcriptional activity with luciferase reporter gene assays.
The longer allele has lower transcriptional activity than the shorter allele in SK-N-MC, SH-SY5Y, HEK293, and HeLa cell lines.
This evidence suggests that the duplication might have a role in regulating the expression of the DRD4 gene and provides an understanding of the biological mechanisms underlying the etiology of neuropsychiatric disorders such as ADHD, schizophrenia, and metamphetamine abuse.
在人类多巴胺D(4)受体基因(DRD4)的5'侧翼区域已鉴定出几种多态性,包括串联重复多态性。这包括一个120个碱基对的重复序列,已知在世界各地的不同人群中具有不同的等位基因频率。此外,各种研究已经揭示了与注意力缺陷多动障碍的连锁证据以及与精神分裂症和甲基苯丙胺滥用的关联。DRD4基因5'调控区域的多态性位置以及它由潜在转录因子结合位点组成这一事实表明,它可能赋予等位基因不同的转录活性。
我们用瞬时转染方法在四种人类细胞系中研究了这种基因变异的功能效应,然后用荧光素酶报告基因测定法评估转录活性。
在SK-N-MC、SH-SY5Y、HEK293和HeLa细胞系中,较长等位基因的转录活性低于较短等位基因。
这一证据表明该重复可能在调节DRD4基因的表达中起作用,并有助于理解诸如注意力缺陷多动障碍、精神分裂症和甲基苯丙胺滥用等神经精神疾病病因背后的生物学机制。