首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Haplotyping strategy highlights the specificity of FTO gene association with polycystic ovary syndrome in Tunisian women population
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Haplotyping strategy highlights the specificity of FTO gene association with polycystic ovary syndrome in Tunisian women population

机译:单倍型策略突显了突尼斯女性人群中FTO基因与多囊卵巢综合征的关联性

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摘要

The FTO (fat mass and obesity associated) gene was associated with different metabolic disorders in populations from different origins but with great difference between African and non-African populations. North-African populations combine many genetic backgrounds, among which African, Berber and Caucasian components, which makes North-Africans a good model for studying the genetic association of FTO. In the present investigation we explored the association of FTO gene with polycystic ovary syndrome (PCOS) in a population from Tunisia (n = 278). Single nucleotide polymorphisms (SNPs) used in this study were previously associated in non-African populations: rs8050136 (A/C), rs9939609 (A/T), rs9930506 (G/A), or in both African and non-African populations: rs8057044 (A/G). Genotyping was performed by allelic discrimination method on StepOne real-time PCR system or KASPar technology. Linkage disequilibrium (LD) pattern was assessed by HAPLOVIEW and reconstruction of haplotypes was performed by PHASE, while statistical analyses were performed using StatView and GoldenHelix programs. Among the 13 haplotypes in the population, three (h1, h7 and h13) were strongly associated with PCOS notably h13 (P <0.0001, 0R95%CI = 0.040 [0.005-0294]) while SNPs display weaker association. Moreover the LD pattern in FTO in the Tunisian population (r(2) index) was intermediary between those of Caucasian and Africans. This highlights the need for studying the genetics of complex disorders in the North-African populations taking into-account the haplotype structure of candidate loci more than SNPs taken alone. (C) 2014 Elsevier B.V. All rights reserved.
机译:FTO(与肥胖和肥胖相关的基因)基因与不同来源人群的代谢紊乱有关,但非洲人群与非非洲人群差异很大。北美人口具有许多遗传背景,其中包括非洲人,柏柏尔人和高加索人,这使得北非成为研究FTO遗传关联的良好模型。在本研究中,我们探讨了突尼斯(n = 278)人群中FTO基因与多囊卵巢综合征(PCOS)的关联。这项研究中使用的单核苷酸多态性(SNP)以前在非非洲人群中存在:rs8050136(A / C),rs9939609(A / T),rs9930506(G / A),或者在非洲和非非洲人群中都存在: rs8057044(A / G)。通过等位基因鉴别方法在StepOne实时PCR系统或KASPar技术上进行基因分型。通过HAPLOVIEW评估连锁不平衡(LD)模式,并通过PHASE进行单倍型重建,同时使用StatView和GoldenHelix程序进行统计分析。在人口的13个单倍型中,三个(h1,h7和h13)与PCOS密切相关,尤其是h13(P <0.0001,0R95%CI = 0.040 [0.005-0294]),而SNPs显示较弱的关联。此外,突尼斯人在FTO中的LD模式(r(2)指数)介于高加索人和非洲人之间。这突出表明,有必要研究北非人口中复杂疾病的遗传学,而不是单独考虑SNP来考虑候选基因座的单倍型结构。 (C)2014 Elsevier B.V.保留所有权利。

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