哈萨克族维生素d受体(VDR)基因rs2228570单核苷酸多态性频率

V. Protas, G. Pogossyan, Constantin Grigoryevich Li, M. Danilenko
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摘要

本文报道了卡拉干达地区哈萨克族维生素D受体(VDR)基因rs2228570单核苷酸多态性(SNP)基因型和个体等位基因频率的研究结果。该SNP采用TaqMan技术实时聚合酶链反应测定。该研究的相关性是由于rs2228570的遗传变异影响了VDR蛋白的合成及其作为调节其他基因表达的转录因子的活性。这一机制决定了个体rs2228570基因型或等位基因与各种疾病的易感性、病程和结局的关联。多态性的频率可能取决于种族。研究结果显示,哈萨克族人rs2228570 SNP最常见的基因型为AG(32.8%)和GG(25.2%)。最罕见的是纯合子TT(1.7%)和CC(0.8%)。本研究首次同时检测到所有rs2228570等位基因的频率。G等位基因为优势等位基因(51.3%),A等位基因较少(31.0%),C和T等位基因最罕见(分别为11.8%和5.9%)。该SNP作为影响人体对包括COVID-19在内的各种疾病易感性的可能因素,其进一步研究的潜在价值得到了体现。
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Frequency of rs2228570 single nucleotide polymorphism of Vitamin-D Receptor (VDR) gene among the Kazakh ethnic group
The article presents the results of the study of vitamin D receptor (VDR) gene rs2228570 single nucleotide polymorphism (SNP) genotypes and individual alleles frequency among the Kazakh ethnic group representatives living in the Karaganda region. This SNP was determined by real-time polymerase chain reaction using TaqMan technology. The study relevance is due to the fact that genetic variations in rs2228570 affect the synthesis of the VDR protein and its activity as a transcription factor that regulates the expression of other genes. This mechanism determines the association of individual rs2228570 genotypes or alleles with susceptibility, course, and outcomes of various diseases. The polymorphism frequency may be depending on ethnicity. According to the study results, the most common genotypes of rs2228570 SNP among the Kazakhs were AG (32.8 %) and GG (25.2 %). The rarest are homozygotes TT (1.7 %) and CC (0.8 %). The frequency of all rs2228570 alleles was detected simultaneously in the present study for the first time. G became the predominant allele (51.3 %), less common was A (31.0 %), and the C and T alleles were the rarest (11.8 % and 5.9 %, respectively). The potential value of this SNP further study as a possible factor influencing the body’s susceptibility to various diseases, including COVID-19, is shown.
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