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通过同源性分析和生物信息学分析,将 Fob3b 基因在小鼠第 15 号染色体上的一个主效 QTL 分解为两个紧密连锁的基因座。

Congenic and bioinformatics analyses resolved a major-effect Fob3b QTL on mouse Chr 15 into two closely linked loci.

机构信息

Department of Animal Science, Biotechnical Faculty, University of Ljubljana, Groblje 3, 1230, Domzale, Slovenia.

出版信息

Mamm Genome. 2010 Apr;21(3-4):172-85. doi: 10.1007/s00335-010-9252-z. Epub 2010 Mar 5.

Abstract

We previously identified a Chr 15 quantitative trait locus (QTL) Fob3b in lines of mice selected for high (Fat line) and low (Lean line) body fat content that represent a unique model of polygenic obesity. Here we genetically dissected the Fob3b interval by analyzing the phenotypes of eight overlapping congenic lines and four F(2) congenic intercrosses and prioritized candidates by bioinformatics approaches. Analyses revealed that the Fob3b QTL consists of at least two separate linked QTLs Fob3b1 and Fob3b2. They exhibit additive inheritance and are linked in coupling with alleles originating from the Lean line, decreasing obesity-related traits. In further analyses, we focused on Fob3b1 because it had a larger effect on obesity-related traits than Fob3b2, e.g., the difference between homozygotes for adiposity index (ADI) percentage was 1.22 and 0.77% for Fob3b1 and Fob3b2, respectively. A set of bioinformatics tools was used to narrow down positional candidates from 85 to 4 high-priority Fob3b1 candidates. A previous single Fob3b QTL was therefore resolved into another two closely linked QTLs, confirming the fractal nature of QTLs mapped at low resolution. The interval of the original Fob3b QTL was narrowed from 22.39 to 4.98 Mbp for Fob3b1 and to 7.68 Mbp for Fob3b2, which excluded the previously assigned candidate squalene epoxidase (Sqle) as the causal gene because it maps proximal to refined Fob3b1 and Fob3b2 intervals. A high-resolution map along with prioritization of Fob3b1 candidates by bioinformatics represents an important step forward to final identification of the Chr 15 obesity QTL.

摘要

我们之前在选择高脂肪(Fat 品系)和低脂肪(Lean 品系)含量的小鼠品系中鉴定了一个 Chr15 数量性状位点(QTL)Fob3b,该品系代表了一种独特的多基因肥胖模型。在这里,我们通过分析八个重叠的近交系和四个 F2 近交系杂交的表型,对 Fob3b 区间进行了遗传剖析,并通过生物信息学方法对候选基因进行了优先级排序。分析表明,Fob3b QTL 至少由两个独立的连锁 QTL Fob3b1 和 Fob3b2 组成。它们表现出加性遗传,与来自 Lean 品系的等位基因连锁,降低了与肥胖相关的特征。在进一步的分析中,我们专注于 Fob3b1,因为它对与肥胖相关的特征的影响大于 Fob3b2,例如,Fob3b1 和 Fob3b2 的肥胖指数(ADI)百分比的纯合子之间的差异分别为 1.22%和 0.77%。一组生物信息学工具用于将位置候选者从 85 个缩小到 4 个 Fob3b1 的高优先级候选者。因此,一个先前的单一 Fob3b QTL 被解析为另外两个紧密连锁的 QTL,证实了在低分辨率下映射的 QTL 的分形性质。原始 Fob3b QTL 的间隔从 Fob3b1 的 22.39 到 4.98 Mbp 缩小到 Fob3b2 的 7.68 Mbp,排除了先前分配的候选 squalene epoxidase (Sqle) 作为候选基因,因为它位于精细 Fob3b1 和 Fob3b2 区间的近端。沿着 Chr15 肥胖 QTL 的高分辨率图谱以及通过生物信息学对 Fob3b1 候选基因进行优先级排序,是最终确定该 QTL 的重要一步。

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