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Identification and Replication of a Novel Obesity Locus on Chromosome 1q24 in Isolated Populations of Cilento

机译:鉴定和复制孤立的奇伦托人口染色体1q24上的新型肥胖基因座。

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OBJECTIVE-Obesity is a complex trait with a variety of genetic susceptibility variants. Several loci linked to obesity and/or obesity-related traits have been identified, and relatively few regions have been replicated. Studying isolated populations can be a useful approach to identify rare variants that will not be detected with whole-genome association studies in large populations. RESEARCH DESIGN AND METHODS-Random individuals were sampled from Campora, an isolated village of the Cilento area in South Italy, phenotyped for BMI, and genotyped using a dense microsatellite marker map. An efficient pedigree-breaking strategy was applied to perform genome-wide linkage analyses of both BMI and obesity. Significance was assessed with ad hoc simulations for the two traits and with an original local false discovery rate approach to quantitative trait linkage analysis for BMI. A genealogy-corrected association test was performed for a single nucleotide polymorphism located in one of the linkage regions. A replication study was conducted in the neighboring village of Gioi. RESULTS-A new locus on chrlq24 significantly linked to BMI was identified in Campora. Linkage at the same locus is suggested with obesity. Three additional loci linked to BMI were also detected, including the locus including the INSIG2 gene region. No evidence of association between the rs7566605 variant and BMI or obesity was found. In Gioi, the linkage on chrlq24 was replicated with both BMI and obesity. CONCLUSIONS-Overall, our results confirm that successful linkage studies can be accomplished in these populations both to replicate known linkages and to identify novel quantitative trait linkages.
机译:目标肥胖是具有多种遗传易感性变异的复杂性状。已经确定了与肥胖和/或肥胖相关性状相关的几个基因座,并且已经复制了相对较少的区域。研究孤立的种群可能是一种有用的方法,可以识别在大种群中无法通过全基因组关联研究检测到的稀有变异。研究设计和方法-随机个体是从意大利南部奇伦托地区一个孤立的村庄Campora取样的,表型为BMI,并使用密集的微卫星标记图进行基因分型。一种有效的谱系突破策略被用于对BMI和肥胖症进行全基因组连锁分析。通过对这两个性状的临时模拟以及对BMI进行定量性状连锁分析的原始本地错误发现率方法,评估了重要性。对位于一个连接区域中的单核苷酸多态性进行了族谱校正关联测试。在邻近的Gioi村进行了复制研究。结果-在坎波拉(Campora)发现了chrlq24上一个与BMI显着相关的新基因座。肥胖者建议在同一基因座处连锁。还检测到三个与BMI相关的基因座,包括包括INSIG2基因区域的基因座。未发现rs7566605变体与BMI或肥胖之间存在关联的证据。在Gioi中,chrlq24上的连锁与BMI和肥胖症均重复存在。结论总体而言,我们的结果证实,可以在这些种群中完成成功的连锁研究,以复制已知的连锁并确定新颖的数量性状连锁。

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