Identification of CAD candidate genes in GWAS loci and their expression in vascular cells

被引:80
作者
Erbilgin, Ayca [1 ]
Civelek, Mete [2 ]
Romanoski, Casey E. [3 ]
Pan, Calvin [2 ]
Hagopian, Raffi [2 ]
Berliner, Judith A. [4 ]
Lusis, Aldons J. [1 ,2 ,3 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
coronary artery disease; genome-wide association study; atherosclerosis; genetics; endothelium; smooth muscle cells; macrophages; GENOME-WIDE ASSOCIATION; CORONARY-ARTERY-DISEASE; SUBTILISIN/KEXIN TYPE 9; N-ACETYLGALACTOSAMINYLTRANSFERASE; SUSCEPTIBILITY LOCI; SERINE RACEMASE; ATHEROSCLEROSIS; ACTIVATION; MIGRATION; VARIANTS;
D O I
10.1194/jlr.M037085
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recent genome-wide association studies (GWAS) have identified 35 loci that significantly associate with coronary artery disease (CAD) susceptibility. The majority of the genes represented in these loci have not previously been studied in the context of atherosclerosis. To characterize the roles of these candidate genes in the vessel wall, we determined their expression levels in endothelial, smooth muscle, and macrophage cells isolated from healthy, prelesioned, and lesioned mouse aortas. We also performed expression quantitative locus (eQTL) mapping of these genes in human endothelial cells under control and proatherogenic conditions. Of the 57 genes studied, 31 were differentially expressed in one or more cell types in disease state in mice, and the expression levels of 8 were significantly associated with the CAD SNPs in human cells, 7 of which were also differentially expressed in mice. By integrating human and mouse results, we predict that PPAP2B, GALNT4, MAPKAPK5, TCTN1, SRR, SNF8, and ICAM1 play a causal role in the susceptibility to atherosclerosis through a role in the vasculature. Additionally, we highlight the genetic complexity of a subset of CAD loci through the differential expression of multiple candidate genes per locus and the involvement of genes that lie outside linkage disequilibrium blocks.
引用
收藏
页码:1894 / 1905
页数:12
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