首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Fine mapping reveals sex bias in quantitative trait loci affecting growth, skeletal size and obesity-related traits on mouse chromosomes 2 and 11.
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Fine mapping reveals sex bias in quantitative trait loci affecting growth, skeletal size and obesity-related traits on mouse chromosomes 2 and 11.

机译:精细定位揭示了数量性状基因座中的性别偏见,影响小鼠染色体2和11的生长,骨骼大小和肥胖相关性状。

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Previous speed congenic analysis has suggested that the expression of growth and obesity quantitative trait loci (QTL) on distal mouse chromosomes (MMU) 2 and 11, segregating between the CAST/EiJ (CAST) and C57BL/6J-hg/hg (HG) strains, is dependent on sex. To confirm, fine map, and further evaluate QTL x sex interactions, we constructed congenic by recipient F2 crosses for the HG.CAST-(D2Mit329-D2Mit457)N(6) (HG2D) and HG.CAST-(D11Mit260-D11Mit255)N(6) (HG11) congenic strains. Over 700 F2 mice were densely genotyped and phenotyped for a panel of 40 body and organ weight, skeletal length, and obesity-related traits at 9 weeks of age. Linkage analysis revealed 20 QTL affecting a representative subset of phenotypes in HG2DF2 and HG11F2 mice. The effect of sex was quantified by comparing two linear models: the first model included sex as an additive covariate and the second incorporated sex as an additive and an interactive covariate. Of the 20 QTL, 8 were sex biased, sex specific, or sex antagonistic. Most traits were regulated by single QTL; however, two closely linked loci were identified for five traits in HG2DF2 mice. Additionally, the confidence intervals for most QTL were significantly reduced relative to the original mapping results, setting the stage for quantitative trait gene (QTG) discovery. These results highlight the importance of assessing the contribution of sex in complex trait analyses.
机译:先前的速度同基因分析表明,生长和肥胖定量特征基因座(QTL)在远端小鼠染色体(MMU)2和11上的表达,在CAST / EiJ(CAST)和C57BL / 6J-hg / hg(HG)之间分离应变,取决于性别。为了确认,精细定位并进一步评估QTL x性别相互作用,我们通过受体F2杂交构建了HG.CAST-(D2Mit329-D2Mit457)N(6)(HG2D)和HG.CAST-(D11Mit260-D11Mit255)N (6)(HG11)同基因菌株。在9周龄时,对700多只F2小鼠进行了密集的基因分型和表型分析,以显示40种体重和器官重量,骨骼长度以及与肥胖相关的特征。连锁分析显示20个QTL影响HG2DF2和HG11F2小鼠表型的代表性子集。通过比较两个线性模型来量化性别的影响:第一个模型包括性作为加性协变量,第二个模型包含性作为加性和交互式协变量。在20个QTL中,有8个存在性别偏见,性别特定或性别对立。大多数性状受单一QTL调控。但是,在HG2DF2小鼠中发现了两个密切相关的基因座,涉及五个性状。此外,相对于原始作图结果,大多数QTL的置信区间显着降低,为定量性状基因(QTG)发现奠定了基础。这些结果突出了评估性别在复杂性格分析中的作用的重要性。

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