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Research Article Free access | 10.1172/JCI1748

Genetic loci controlling body fat, lipoprotein metabolism, and insulin levels in a multifactorial mouse model.

M Mehrabian, P Z Wen, J Fisler, R C Davis, and A J Lusis

Department of Medicine, University of California, Los Angeles, California 90095, USA.

Find articles by Mehrabian, M. in: PubMed | Google Scholar

Department of Medicine, University of California, Los Angeles, California 90095, USA.

Find articles by Wen, P. in: PubMed | Google Scholar

Department of Medicine, University of California, Los Angeles, California 90095, USA.

Find articles by Fisler, J. in: PubMed | Google Scholar

Department of Medicine, University of California, Los Angeles, California 90095, USA.

Find articles by Davis, R. in: PubMed | Google Scholar

Department of Medicine, University of California, Los Angeles, California 90095, USA.

Find articles by Lusis, A. in: PubMed | Google Scholar

Published June 1, 1998 - More info

Published in Volume 101, Issue 11 on June 1, 1998
J Clin Invest. 1998;101(11):2485–2496. https://doi.org/10.1172/JCI1748.
© 1998 The American Society for Clinical Investigation
Published June 1, 1998 - Version history
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Abstract

We analyzed the inheritance of body fat, leptin levels, plasma lipoprotein levels, insulin levels, and related traits in an intercross between inbred mouse strains CAST/Ei and C57BL/6J. CAST/Ei mice are unusually lean, with only approximately 8% of body weight as fat, whereas C57BL/6J mice have approximately 18% body fat. Quantitative trait locus analysis using > 200 F2 mice revealed highly significant loci (lod scores > 4.3) on chromosomes 2 (three separate loci) and 9 that contribute to mouse fat-pad mass for mice on a high-fat diet. Some loci also influenced plasma lipoprotein levels and insulin levels either on chow or high-fat diets. Two loci for body fat and lipoprotein levels (on central and distal chromosome 2) coincided with a locus having strong effects on hepatic lipase activity, an activity associated with visceral obesity and lipoprotein levels in humans. A locus contributing to plasma leptin levels (lod score 5.3) but not obesity was identified on chromosome 4, near the leptin receptor gene. These data identify candidate regions and candidate genes for studies of human obesity and diabetes, and suggest obesity is highly complex in terms of the number of genetic factors involved. Finally, they support the existence of specific genetic interactions between body fat, insulin metabolism, and lipoprotein metabolism.

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