4.7 Article

High-Resolution Association Mapping of Atherosclerosis Loci in Mice

Journal

ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
Volume 32, Issue 8, Pages 1790-U216

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/ATVBAHA.112.253864

Keywords

atherosclerosis; gene expression; genetic techniques; genetically altered mice

Funding

  1. National Institutes of Health/National Heart, Lung, and Blood Institute [PO1 HL30568]
  2. [K99 HL102223]

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The purpose of this study was to fine map previously identified quantitative trait loci affecting atherosclerosis in mice using association analysis. Methods and Results-We recently showed that high-resolution association analysis using common inbred strains of mice is feasible if corrected for population structure. To use this approach for atherosclerosis, which requires a sensitizing mutation, we bred human apolipoprotein B-100 transgenic mice with 22 different inbred strains to produce F1 heterozygotes. Mice carrying the dominant transgene were tested for association with high-density single nucleotide polymorphism maps. Here, we focus on high-resolution mapping of the previously described atherosclerosis 30 locus on chromosome 1. Compared with the previous linkage analysis, association improved the resolution of the atherosclerosis 30 locus by more than an order of magnitude. Using expression quantitative trait locus analysis, we identified one of the genes in the region, desmin, as a strong candidate. Conclusion-Our high-resolution mapping approach accurately identifies and fine maps known atherosclerosis quantitative trait loci. These results suggest that high-resolution genome-wide association analysis for atherosclerosis is feasible in mice. (Arterioscler Thromb Vasc Biol. 2012;32:1790-1798.)

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