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一个用于解析小鼠复杂性状的高分辨率关联图谱面板。

A high-resolution association mapping panel for the dissection of complex traits in mice.

机构信息

Department of Medicine/Division of Cardiology, David Geffen School of Medicine, University of California, Los Angeles, California 90095, USA.

出版信息

Genome Res. 2010 Feb;20(2):281-90. doi: 10.1101/gr.099234.109. Epub 2010 Jan 6.

Abstract

Systems genetics relies on common genetic variants to elucidate biologic networks contributing to complex disease-related phenotypes. Mice are ideal model organisms for such approaches, but linkage analysis has been only modestly successful due to low mapping resolution. Association analysis in mice has the potential of much better resolution, but it is confounded by population structure and inadequate power to map traits that explain less than 10% of the variance, typical of mouse quantitative trait loci (QTL). We report a novel strategy for association mapping that combines classic inbred strains for mapping resolution and recombinant inbred strains for mapping power. Using a mixed model algorithm to correct for population structure, we validate the approach by mapping over 2500 cis-expression QTL with a resolution an order of magnitude narrower than traditional QTL analysis. We also report the fine mapping of metabolic traits such as plasma lipids. This resource, termed the Hybrid Mouse Diversity Panel, makes possible the integration of multiple data sets and should prove useful for systems-based approaches to complex traits and studies of gene-by-environment interactions.

摘要

系统遗传学依赖于常见的遗传变异来阐明导致复杂疾病相关表型的生物网络。老鼠是此类方法的理想模式生物,但由于映射分辨率低,连锁分析的成功率仅适中。由于群体结构和映射解释方差小于 10%的性状的能力不足(典型的小鼠数量性状位点[QTL]),老鼠的关联分析有可能具有更好的分辨率。我们报告了一种新的关联映射策略,该策略结合了经典近交系用于映射分辨率和重组近交系用于映射能力。我们使用混合模型算法来校正群体结构,通过映射超过 2500 个顺式表达 QTL 来验证该方法,其分辨率比传统 QTL 分析窄一个数量级。我们还报告了代谢性状(如血浆脂质)的精细映射。该资源称为杂种鼠多样性面板,使多个数据集的整合成为可能,并且应该对复杂性状的基于系统的方法和基因-环境相互作用的研究很有用。

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