Suppr超能文献

以多巴胺(D4)受体VNTR多态性为特征的印度族裔人群。

Indian ethnic populations characterized by dopamine (D4) receptor VNTR polymorphism.

作者信息

Ghosh Anu, Seshadri M

机构信息

Low Level Radiation Studies Section, Biosciences Group, Bhabha Atomic Research Centre, Trombay, Mumbai 400 085, India.

出版信息

Ann Hum Biol. 2005 Sep-Oct;32(5):574-84. doi: 10.1080/03014460500228790.

Abstract

BACKGROUND

The human dopamine receptor D4 gene (DRD4) contains a 48-bp tandem repeat in exon 3 and shows alleles varying between repeats 2 and 11. The gene shows a high level of expression in the prefrontal cortex of the brain and association of particular alleles of this locus with various neuropsychiatric and personality disorders have been reported.

OBJECTIVE

The present study reports allele frequency distribution at the DRD4 variable number tandem repeat (VNTR) locus among five ethnic populations of India. This background information is fundamental to the field of pharmacogenetics for disease susceptibility and association studies.

SUBJECTS AND METHODS

Three hundred and thirty two healthy unrelated adult individuals belonging to five ethnic groups: Konkanastha Brahmins, Marathas, Ezhavas, Nairs and Muslims, have been typed. Genomic DNA, extracted from peripheral blood, was PCR amplified using a two-enzyme system. The use of ALF Express DNA sequencer was found to be helpful for large-scale population genotyping. Statistical analysis was performed using the POPGENE and DISPAN programs.

RESULTS

A total of eight alleles ranging from repeat 2 to repeat 9 were observed. Allele 4 was the predominant allele among all the five populations, consistent with the data on other world populations. A rare allele 9 was detected exclusively among Marathas. The observed heterozygosity was low, ranging from 0.38 to 0.54 while other parameters like Polymorphism Information Content (PIC) and Power of Discrimination (PD) showed moderate values. The populations were in genetic equilibrium when tested under Hardy-Weinberg expectations.

CONCLUSION

The allele frequency estimates for DRD4 provided here will contribute towards developing an informative database for this functionally relevant locus. This will prove useful when studying the association between genetic factors and pathogenesis of disease in Indian populations and will address the concern of biased results of association due to population admixtures.

摘要

背景

人类多巴胺受体D4基因(DRD4)在第3外显子中含有一个48碱基对的串联重复序列,其等位基因在2到11次重复之间变化。该基因在大脑前额叶皮质中表现出高水平的表达,并且已经报道了该位点的特定等位基因与各种神经精神疾病和人格障碍之间的关联。

目的

本研究报告了印度五个民族群体中DRD4可变数目串联重复序列(VNTR)位点的等位基因频率分布。这些背景信息对于疾病易感性和关联研究的药物遗传学领域至关重要。

对象与方法

对属于五个民族群体的332名健康无关成年个体进行了基因分型,这五个民族群体分别是:科纳克斯坦婆罗门、马拉地人、埃扎瓦人、奈尔人和穆斯林。从外周血中提取基因组DNA,使用双酶系统进行PCR扩增。发现使用ALF Express DNA测序仪有助于大规模群体基因分型。使用POPGENE和DISPAN程序进行统计分析。

结果

共观察到8个等位基因,重复次数从2到9次。等位基因4是所有五个群体中的主要等位基因,这与其他世界群体的数据一致。仅在马拉地人群体中检测到一个罕见的等位基因9。观察到的杂合度较低,范围从0.38到0.54,而其他参数如多态性信息含量(PIC)和鉴别力(PD)显示为中等值。在哈迪-温伯格期望下进行测试时,这些群体处于遗传平衡状态。

结论

此处提供的DRD4等位基因频率估计值将有助于为这个功能相关位点建立一个信息丰富的数据库。这在研究印度人群体中遗传因素与疾病发病机制之间的关联时将被证明是有用的,并且将解决由于群体混合导致的关联结果有偏差的问题。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验