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Journal of Lipid Research, Vol. 45, 2063-2070, November 2004
Copyright © 2004 by American Society for Biochemistry and Molecular Biology



,

* Department of Biostatistics, Section on Statistical Genetics, University of Alabama, Birmingham, AL 35294
Clinical Nutrition Research Center, University of Alabama, Birmingham, AL 35294
Rowe Program in Genetics, University of California, Davis, CA 95616
** Department of Nutrition, University of California, Davis, CA 95616

Department of Pediatrics and Section of Neurobiology, Physiology, and Behavior, University of California, Davis, CA 95616
1 To whom correspondence should be addressed. e-mail: chwarden{at}ucdavis.edu
BSB mice exhibit a wide range of obesity despite being produced by a backcross of lean C57BL/6J (B) x lean Mus spretus (SPRET/Pt) F1 animals x B. Previous linkage studies identified a quantitative trait locus (QTL) on mouse chromosome 7 with coincident peaks for hepatic lipase activity, obesity, and plasma cholesterol. However, these mice were not analyzed for gene x gene epistasis. Hepatic lipase activity is correlated with obesity and plasma cholesterol levels. In this study, we identified QTLs for plasma hepatic lipase activity with three statistical mapping methods: maximum likelihood interval mapping, Bayesian nonepistatic mapping, and Bayesian epistatic mapping. Bayesian epistatic mapping detected not only the QTL on chromosome 7 but also an additional QTL on chromosome 3, which has a weak main effect but a strong interaction with chromosome 7. SPRET/Pt alleles of the QTL on each chromosome promote hepatic lipase activity.
The proportion of phenotypic variance explained by the epistatic effect is higher than that explained by the main effect of the QTL on chromosome 7.
Abbreviations: cM, centimorgan; HPD, high posterior density; MCMC, Markov chain Monte Carlo; QTL, quantitative trait locus
Supplementary key words gene x gene mouse obesity hepatic lipase Bayesian quantitative trait locus
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