Laboratory of Genetics, Immunology and Human Pathology, Faculty of Science of Tunis, University of Tunis El Manar, 2092 Tunis, Tunisia.
Laboratory of Genetics, Immunology and Human Pathology, Faculty of Science of Tunis, University of Tunis El Manar, 2092 Tunis, Tunisia; High Institute of Biotechnology, University of Monastir, 5000 Monastir, Tunisia.
Gene. 2019 May 15;696:186-196. doi: 10.1016/j.gene.2019.02.021. Epub 2019 Feb 18.
The COMT gene encodes for catechol-O-methyl-transferase, an enzyme playing a major role in regulation of synaptic catecholamine neurotransmitters. Investigating 4 markers of the COMT gene (rs2020917, rs4818, rs4680, rs9332377) in 6 Tunisian populations and a pool of Libyans. Our objective was to determine the distribution of allelic, genotypic and haplotypic frequencies by comparison to other populations of the 1000 genomes project and 59 populations from the Kidd Lab dataset. The allelic frequencies established for these SNPs in the North African populations are similar to those of Europeans and South Asians. Linkage disequilibrium between these SNPs and haplotypes frequencies are different between populations whose clustering in principal components analysis (PCA) according to their geographic origin was more significant using haplotypic frequencies. COMT activity prediction by haplotypes genotyping could be limited to rs4818-rs4680 micro-haplotypes. The Low activity haplotype (CG) displays the highest frequency in African populations (55%), in the 59 Kidd Lab populations we found also that Sub-Saharan Africans, Native Americans, and some East Asian and Pacific Island populations all have frequencies in the 50-81% range for (CG) where as its lowest frequency was found in Europeans (10%), this results have been also confirmed for Southwest Asians. North Africans and South Asians with intermediate frequencies have approximately similar values (20% and 25%). Europeans show the highest frequencies of haplotypes with predicted High and Medium activity in contrast to Africans. North Africans and South Asians present similar results for all the category of the COMT activity prediction by haplotypes genotyping. The high level of genetic diversity of COMT haplotypes, not only allows distinction between populations according to their history settlement, origin and ethnicity, it constitutes a basis for studies of association of the COMT gene polymorphism with pathologies, drugs response and for forensic investigation in North African populations.
COMT 基因编码儿茶酚-O-甲基转移酶,该酶在调节突触儿茶酚胺神经递质方面起着主要作用。在 6 个突尼斯人群和利比亚人群中研究了 COMT 基因的 4 个标记物(rs2020917、rs4818、rs4680、rs9332377)。我们的目的是通过与 1000 基因组计划的其他人群和 Kidd 实验室数据集的 59 个人群进行比较,确定等位基因、基因型和单倍型频率的分布。这些 SNP 在北非人群中的等位基因频率与欧洲人和南亚人相似。这些 SNP 之间的连锁不平衡和单倍型频率在人群之间不同,根据其地理来源对人群进行主成分分析(PCA)聚类时,使用单倍型频率更为显著。通过单倍型基因分型预测 COMT 活性可能仅限于 rs4818-rs4680 微单倍型。低活性单倍型(CG)在非洲人群中的频率最高(55%),在 59 个 Kidd 实验室人群中,我们还发现撒哈拉以南非洲人、美洲原住民以及一些东亚和太平洋岛屿人群的(CG)频率范围在 50-81%,而其频率最低的是欧洲人(10%),这一结果也得到了西南亚人的证实。北非和南亚人的中间频率具有相似的值(20%和 25%)。与非洲人相比,欧洲人显示出具有预测高和中等活性的单倍型的最高频率。北非和南亚人在 COMT 活性预测的所有单倍型类别中均表现出相似的结果。COMT 单倍型的遗传多样性水平很高,不仅可以根据人群的历史定居点、起源和种族来区分人群,还可以为 COMT 基因多态性与疾病、药物反应的关联研究以及北非人群的法医学调查提供基础。