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Usefulness of COMT gene polymorphisms in North African populations
- Source :
- Gene. 696:186-196
- Publication Year :
- 2019
- Publisher :
- Elsevier BV, 2019.
-
Abstract
- 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. This work was partially supported by the Tunisian Ministry of Higher Education and Scientific Research as well as by the University of Tunis El Manar . Special thanks go to the thousands of individuals around the world who volunteered to give blood and saliva samples to made this study possible. Scopus
- Subjects :
- Forensic Genetics
0301 basic medicine
Linkage disequilibrium
Acclimatization
Black People
rs4680
Single-nucleotide polymorphism
Micro-haplotypes
Biology
Catechol O-Methyltransferase
Polymorphism, Single Nucleotide
Linkage Disequilibrium
03 medical and health sciences
0302 clinical medicine
Africa, Northern
Gene Frequency
Genetics
Humans
1000 Genomes Project
Allele
Genotyping
Alleles
Genetic diversity
Haplotype
General Medicine
North Africa
COMT
Healthy Volunteers
030104 developmental biology
Haplotypes
Pharmacogenetics
030220 oncology & carcinogenesis
Subjects
Details
- ISSN :
- 03781119
- Volume :
- 696
- Database :
- OpenAIRE
- Journal :
- Gene
- Accession number :
- edsair.doi.dedup.....8b6e4b60c55c55d29a381309e51cef9c