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多巴胺D4受体基因的5'非翻译区与注意缺陷多动障碍

5'-untranslated region of the dopamine D4 receptor gene and attention-deficit hyperactivity disorder.

作者信息

Barr C L, Feng Y, Wigg K G, Schachar R, Tannock R, Roberts W, Malone M, Kennedy J L

机构信息

Department of Psychiatry, The Toronto Western Hospital, Ontario, Canada.

出版信息

Am J Med Genet. 2001 Jan 8;105(1):84-90.

Abstract

Recently the molecular genetic basis of attention-deficit hyperactivity disorder (ADHD) has been the focus of a number of studies with the majority of these investigating the role of dopamine system genes. A great deal of attention has been focused on the possible involvement of the dopamine D4 receptor gene (DRD4) following a report of an association of ADHD with the allele containing seven copies of the 48-bp repeat in the third exon. In this paper we extended the search for the molecular explanation for the observed association by testing three polymorphisms in the region 5' to the dopamine receptor D4 gene transcription start site for linkage to ADHD. We specifically targeted polymorphisms in the region 5' to the start site of transcription as DNA variants in this region could alter the transcription level of the gene and hence the phenotype. We did not observe significant evidence for biased transmission of any of the alleles at these three polymorphisms to ADHD probands using the transmission disequilibrium test. We conclude that these three polymorphisms are not related to the ADHD phenotype.

摘要

最近,注意力缺陷多动障碍(ADHD)的分子遗传基础一直是众多研究的焦点,其中大多数研究都在探究多巴胺系统基因的作用。在一份关于ADHD与第三外显子中包含七个48碱基对重复序列拷贝的等位基因之间关联的报告之后,多巴胺D4受体基因(DRD4)的可能参与受到了极大关注。在本文中,我们通过检测多巴胺受体D4基因转录起始位点5'区域的三个多态性与ADHD的连锁关系,扩大了对观察到的关联进行分子解释的研究范围。我们特别针对转录起始位点5'区域的多态性,因为该区域的DNA变异可能会改变基因的转录水平,进而影响表型。使用传递不平衡检验,我们没有观察到这三个多态性的任何等位基因向ADHD先证者的偏向传递的显著证据。我们得出结论,这三个多态性与ADHD表型无关。

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