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首页> 外文期刊>The Journal of Veterinary Medical Science >QTL mapping of genes controlling plasma insulin and leptin concentrations: metabolic effect of obesity QTLs identified in an F2 intercross between C57BL/6J and DDD.Cg-Ay inbred mice.
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QTL mapping of genes controlling plasma insulin and leptin concentrations: metabolic effect of obesity QTLs identified in an F2 intercross between C57BL/6J and DDD.Cg-Ay inbred mice.

机译:控制血浆胰岛素和瘦素浓度的基因的QTL定位:在C57BL / 6J与DDD.Cg-A y 近交小鼠的F 2 杂交中鉴定的肥胖QTL的代谢作用。

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DDD.Cg-Ay female mice developed massive obesity as compared with B6.Cg-Ay female mice. We previously identified quantitative trait loci (QTLs) for obesity on chromosomes 1, 6, 9 and 17 in F2 female mice, including F2Ay (F2 mice with the Ay allele) and F2 non-Ay mice (F2 mice without the Ay allele), produced by crossing C57BL/6J and DDD.Cg-Ay strains. We here addressed the question whether the obesity QTLs share genetic bases with putative QTLs for plasma glucose, insulin and leptin concentrations. We performed QTL analyses for the first principal component (PC1) extracted from these metabolic measurements to identify the genes that contributed to the comprehensive evaluation of metabolic traits. By single QTL scans, we identified two significant QTLs for insulin concentration on chromosomes 6 and 12, three for leptin concentration on chromosomes 1, 6 and 17, and five for PC1 on chromosomes 1, 6, 12 (two loci) and 17. Although insulin and leptin concentrations and PC1 were not normally distributed in combined F2 mice, results of single QTL scans by parametric and non-parametric methods were very similar. Therefore, QTL scan by the parametric method was performed with the agouti locus genotype as a covariate. A significant QTL x covariate interaction was found for PC1 on chromosome 9. All obesity QTLs had significant metabolic effects. Thus, obesity- and diabetes-related traits in DDD.Cg-Ay mice were largely controlled by QTLs on chromosomes 1, 6, 9, 12 and 17.
机译:与B6.Cg-A y 雌性小鼠相比,DDD.Cg-A y 雌性小鼠出现大量肥胖。我们先前在F 2 雌性小鼠(包括F 2 A y (具有A y 等位基因的F 2 小鼠)和F 2 非A y 小鼠(F通过C57BL / 6J和DDD.Cg-A y 品系杂交产生的 2 小鼠,没有A y 等位基因。我们在这里解决了肥胖QTL是否与假定的QTL具有相同的遗传基础的血浆葡萄糖,胰岛素和瘦素浓度的问题。我们对从这些代谢测量值中提取的第一个主要成分(PC1)进行了QTL分析,以鉴定有助于全面评估代谢性状的基因。通过单次QTL扫描,我们在6号和12号染色体上确定了两个重要的胰岛素浓度QTL,在1号,6号和17号染色​​体上确定了瘦素浓度的三个QTL,在1、6、12号染色体(两个基因座)和17个上的PC1鉴定了五个。在组合的F 2 小鼠中,胰岛素和瘦素的浓度以及PC1均未呈正态分布,通过参数和非参数方法进行的单个QTL扫描结果非常相似。因此,通过参数方法进行的QTL扫描以刺豚鼠基因座基因型为协变量。发现9号染色体上PC1有显着的QTL x协变量相互作用。所有肥胖QTL具有明显的代谢作用。因此,DDD.Cg-A y 小鼠中与肥胖和糖尿病有关的性状主要受1、6、9、12和17号染色​​体上QTL的控制。

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