Mapping eQTLs in the Norfolk Island Genetic Isolate Identifies Candidate Genes for CVD Risk Traits

被引:27
作者
Benton, Miles C. [1 ]
Lea, Rod A. [1 ]
Macartney-Coxson, Donia [2 ]
Carless, Melanie A. [3 ]
Goering, Harald H. [3 ]
Bellis, Claire [3 ]
Hanna, Michelle [1 ,4 ]
Eccles, David [1 ]
Chambers, Geoffrey K. [5 ]
Curran, Joanne E. [3 ]
Harper, Jacquie L. [6 ]
Blangero, John [3 ]
Griffiths, Lyn R. [1 ,4 ]
机构
[1] Griffith Univ, Griffith Hlth Inst, Genom Res Ctr, Southport, Qld 4222, Australia
[2] Kenepuru Sci Ctr, Inst Environm Sci & Res, Wellington 5240, New Zealand
[3] Texas Biomed Res Inst, San Antonio, TX 78227 USA
[4] Queensland Univ Technol, Inst Hlth & Biomed Innovat, Kelvin Grove, Qld 4059, Australia
[5] Victoria Univ Wellington, Sch Biol Sci, Wellington 6140, New Zealand
[6] Malaghan Inst Med Res, Wellington 6242, New Zealand
基金
英国医学研究理事会;
关键词
GENOME-WIDE ASSOCIATION; METHYLENETETRAHYDROFOLATE REDUCTASE GENE; METABOLIC-SYNDROME; LINKAGE ANALYSIS; C677T POLYMORPHISM; CARDIAC METABOLISM; COMMON VARIANTS; LIFE-STYLE; EXPRESSION; LOCI;
D O I
10.1016/j.ajhg.2013.11.004
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cardiovascular disease (CVD) affects millions of people worldwide and is influenced by numerous factors, including lifestyle and genetics. Expression quantitative trait loci (eQTLs) influence gene expression and are good candidates for CVD risk. Founder-effect pedigrees can provide additional power to map genes associated with disease risk. Therefore, we identified eQTLs in the genetic isolate of Norfolk Island (NI) and tested for associations between these and CVD risk factors. We measured genome-wide transcript levels of blood lymphocytes in 330 individuals and used pedigree-based heritability analysis to identify heritable transcripts. eQTLs were identified by genome-wide association testing of these transcripts. Testing for association between CVD risk factors (i.e., blood lipids, blood pressure, and body fat indices) and eQTLs revealed 1,712 heritable transcripts (p < 0.05) with heritability values ranging from 0.18 to 0.84. From these, we identified 200 cis-acting and 70 trans-acting eQTLs (p < 1.84 x 10(-7)) An eQTL-centric analysis of CVD risk traits revealed multiple associations, including 12 previously associated with CVD-related traits. Trait versus eQTL regression modeling identified four CVD risk candidates (NAAA, PAPSS1, NME1, and PRDX1), all of which have known biological roles in disease. In addition, we implicated several genes previously associated with CVD risk traits, including MTHFR and FN3KRP. We have successfully identified a panel of eQTLs in the NI pedigree and used this to implicate several genes in CVD risk. Future studies are required for further assessing the functional importance of these eQTLs and whether the findings here also relate to outbred populations.
引用
收藏
页码:1087 / 1099
页数:13
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