Genetic, epigenetic, and gene-by-diet interaction effects underlie variation in serum lipids in a LG/JxSM/J murine model

被引:20
作者
Lawson, Heather A. [1 ]
Zelle, Kathleen M. [1 ]
Fawcett, Gloria L. [1 ]
Wang, Bing [1 ]
Pletscher, L. Susan [1 ]
Maxwell, Taylor J. [3 ]
Ehrich, Thomas H. [1 ]
Kenney-Hunt, Jane P. [1 ]
Wolf, Jason B. [4 ]
Semenkovich, Clay F. [2 ]
Cheverud, James M. [1 ]
机构
[1] Washington Univ, Sch Med, Dept Anat & Neurobiol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[3] Univ Texas Hlth Sci Ctr Houston, Sch Publ Hlth, Ctr Human Genet, Houston, TX USA
[4] Univ Bath, Dept Biol & Biochem, Bath BA2 7AY, Avon, England
基金
英国生物技术与生命科学研究理事会; 美国国家卫生研究院;
关键词
LG/J by SM/J advanced intercross; cholesterol; free-fatty acid; triglyceride; imprinting; quantitative trait locus; QUANTITATIVE TRAIT LOCI; CARDIOVASCULAR-DISEASE; METABOLIC SYNDROME; LIPOPROTEIN CHOLESTEROL; OBESITY; LINE; RISK; SM/J; ASSOCIATION; ADIPOSITY;
D O I
10.1194/jlr.M006957
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
Variation in serum cholesterol, free-fatty acids, and triglycerides is associated with cardiovascular disease (CVD) risk factors. There is great interest in characterizing the underlying genetic architecture of these risk factors, because they vary greatly within and among human populations and between the sexes. We present results of a genome-wide scan for quantitative trait loci (QTL) affecting serum cholesterol, free-fatty acids, and triglycerides in an F 16 advanced intercross line of LG/J and SM/J (Wustl:LG,SM-G16). Half of the population was fed a high-fat diet and half was fed a relatively low-fat diet. Context-dependent genetic (additive and dominance) and epigenetic (imprinting) effects were characterized by partitioning animals into sex, diet, and sex-by-diet cohorts. Here we examine genetic, environmental, and genetic-by-environmental interactions of QTL overlapping previously identified loci associated with CVD risk factors, and we add to the serum lipid QTL landscape by identifying new loci.-Lawson, H. A., K. M. Zelle, G. L. Fawcett, B. Wang, L. S. Pletscher, T. J. Maxwell, T. H. Ehrich, J. P. Kenney-Hunt, J. B. Wolf, C. F. Semenkovich, and J. M. Cheverud. Genetic, epigenetic, and gene-by-diet interaction effects underlie variation in serum lipids in a LG/JxSM/J murine model. J. Lipid Res. 2010. 51: 2976-2984.
引用
收藏
页码:2976 / 2984
页数:9
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