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TNF 基因中的单核苷酸多态性与食蟹猴肥胖相关表型相关。

Single-nucleotide polymorphisms in the TNF gene are associated with obesity-related phenotypes in vervet monkeys.

机构信息

Department of Pathology, Section on Comparative Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.

出版信息

Obesity (Silver Spring). 2011 Jul;19(7):1427-32. doi: 10.1038/oby.2011.19. Epub 2011 Feb 17.

Abstract

Tumor necrosis factor (TNF) promoter single-nucleotide polymorphisms (SNPs) have been extensively characterized in humans, with numerous reports of associations with obesity-related phenotypes as well an array of infectious, immune-mediated, and inflammatory disease phenotypes. Controlling for the multitude of environmental risk factors in human studies has been a major confounder of efforts to elucidate the role and relative contribution of TNF promoter SNPs. As part of an ongoing initiative to further genetically and phenotypically characterize the St Kitts-origin vervet monkey (Chlorocebus aethiops ssp.) as an animal model of human obesity, we have conducted association analyses between TNF SNPs and previously defined obesity-related phenotypes in 265 pedigreed vervets. We report eight SNPs (-809G, -756A, -352C, -322A, +1285T, +2133T, +2362A, +2405), all contained within the same haplotype block and comprising a single haplotype, to be significantly associated with BMI, waist circumference, total plasma cholesterol (P < 0.05), and high-density lipoprotein-cholesterol (HDL-C) (P < 0.01). This study provides additional validation of the St Kitts-origin vervet model of obesity by demonstrating genetic associations analogous to that shown in humans.

摘要

肿瘤坏死因子 (TNF) 启动子单核苷酸多态性 (SNP) 在人类中得到了广泛的研究,大量研究报告表明其与肥胖相关表型以及一系列感染、免疫介导和炎症性疾病表型有关。在人类研究中,控制多种环境风险因素是阐明 TNF 启动子 SNP 作用和相对贡献的主要混杂因素。作为一项正在进行的计划的一部分,该计划旨在进一步对圣基茨起源的长尾猕猴 (Chlorocebus aethiops ssp.) 进行遗传和表型特征分析,作为人类肥胖的动物模型,我们对 265 只 pedigreed 长尾猕猴进行了 TNF SNP 与之前定义的肥胖相关表型之间的关联分析。我们报告了 8 个 SNP(-809G、-756A、-352C、-322A、+1285T、+2133T、+2362A、+2405),都包含在同一个单倍型块中,并且构成了一个单倍型,与 BMI、腰围、总血浆胆固醇 (P < 0.05) 和高密度脂蛋白胆固醇 (HDL-C) (P < 0.01) 显著相关。这项研究通过证明与人类相似的遗传关联,为肥胖的圣基茨起源长尾猕猴模型提供了额外的验证。

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