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Distribution of cytokine gene single nucleotide polymorphisms among a multi-ethnic Iranian population

机译:细胞因子基因单核苷酸多态性在伊朗多民族人群中的分布

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Background: Cytokine gene single nucleotide polymorphisms (SNPs) are widely used to study susceptibility to complex diseases and as a tool for anthropological studies. Materials and Methods: To investigate cytokine SNPs in an Iranian multi-ethnic population, we have investigated 10 interleukin (IL) SNPs (IL-1β (C-511T, T-31C), IL-2 (G-384T), IL-4 (C-590T), IL-6 (G-174C), IL-8 (T-251A), IL-10 (G-1082A, C-819T, C-592A) and tumor necrosis factor-alpha (TNF-α) (G-308A) in 415 Iranian subjects comprising of 6 different ethnicities. Allelic and genotypic frequencies as well as Hardy-Weinberg equilibrium (HWE) were calculated by PyPop software. Population genetic indices including observed heterozygosity (H o ), expected heterozygosity (H e ), fixation index (F IS ), the effective number of alleles ( N e ) and polymorphism information content (PIC) were derived using Popgene 32 software. Multidimensional scaling (MDS) was constructed using Reynold's genetic distance obtained from the frequencies of cytokine gene polymorphism. Results: Genotypic distributions were consistent with the HWE assumptions, except for 3 loci (IL-4-590, IL-8-251 and IL-10-819) in Fars and 4 loci (IL-4-590, IL-6-174, IL-10-1082 and TNF-α-308) in Turks. Pairwise assessment of allelic frequencies, detected differences at the IL-4-590 locus in Gilakis versus Kurds ( P = 0.028) and Lurs ( P = 0.022). Mazanis and Gilakis displayed the highest (H o = 0.50 ± 0.24) and lowest (H o = 0.34 ± 0.16) mean observed heterozygosity, respectively. Conclusions: MDS analysis of our study population, in comparison with others, revealed that Iranian ethnicities except Kurds and Mazanis were tightly located within a single cluster with closest genetic affinity to Europeans.
机译:背景:细胞因子基因单核苷酸多态性(SNP)被广泛用于研究对复杂疾病的易感性,并作为人类学研究的工具。材料和方法:为了研究伊朗多族裔人群中的细胞因子SNP,我们研究了10种白介素(IL)SNP(IL-1β(C-511T,T-31C),IL-2(G-384T),IL- 4(C-590T),IL-6(G-174C),IL-8(T-251A),IL-10(G-1082A,C-819T,C-592A)和肿瘤坏死因子-α(TNF-用6个不同种族的415名伊朗受试者的α)(G-308A),通过PyPop软件计算了等位基因和基因型频率以及Hardy-Weinberg平衡(HWE),包括观察到的杂合度(H o < / sub>),预期杂合性(H e ),固定指数(F IS ),有效等位基因数(N e )和利用Popgene 32软件推导了多态性信息含量(PIC),利用从细胞因子基因多态性频率获得的雷诺遗传距离构建了多维尺度(MDS),结果:基因型分布与HWE假设一致,除3 l外。 Fars和4个基因座(IL-4-590,IL-6-174,IL-10-1082和TNF-α-308)中的oci(IL-4-590,IL-8-251和IL-10-819)在土耳其人。对等位基因频率的成对评估,在Gilakis与Kurds(P = 0.028)和Lurs(P = 0.022)的IL-4-590位点检测到差异。 Mazanis和Gilakis分别显示最高的平均杂合度(H o = 0.50±0.24)和最低的(H o = 0.34±0.16)。结论:与其他研究对象相比,对我们研究人群的MDS分析显示,除了库尔德人和马扎尼人以外,伊朗族群紧密地位于一个与欧洲人具有最亲近遗传关系的族群中。

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