J. Lipid Res.
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Journal of Lipid Research, Vol. 41, 1936-1946, December 2000
Copyright © 2000 by Lipid Research, Inc.


Original Article

Genetic control of HDL levels and composition in an interspecific mouse cross (CAST/Ei x C57BL/6J)

Margarete Mehrabiana, Lawrence W. Castellania, Ping-Zi Wena, Jack Wonga, Tat Rithapornb, Susan Y. Hamaa, Gregory P. Hougha, David Johnsona, John J. Alberse, Giuliano A. Mottinoa, Joy S. Franka, Mohamad Navaba, Alan M. Fogelmana, and Aldons J. Lusisa,b,c,d
a Department of Medicine, University of California, Los Angeles, CA 90095
b Department of Microbiology and Molecular Genetics, University of California, Los Angeles, CA 90095
c Department of Human Genetics, University of California, Los Angeles, CA 90095
d Molecular Biology Institute, University of California, Los Angeles, CA 90095
e Northwest Lipid Laboratories, Department of Medicine, University of Washington, Seattle, WA 98115

Correspondence to: Aldons J. Lusis

Strain CAST/Ei (CAST) mice exhibit unusually low levels of high density lipoproteins (HDL) as compared with most other strains of mice, including C57BL/6J (B6). This appears to be due in part to a functional deficiency of lecithin:cholesterol acyltransferase (LCAT). LCAT mRNA expression in CAST mice is normal, but the mice exhibit several characteristics consistent with functional deficiency. First, the activity and mass of LCAT in plasma and in HDL of CAST mice were reduced significantly. Second, the HDL of CAST mice were relatively poor in phospholipids and cholesteryl esters, but rich in free cholesterol and apolipoprotein A-I (apoA-I). Third, the adrenals of CAST mice were depleted of cholesteryl esters, a phenotype similar to that observed in LCAT- and acyl-CoA:cholesterol acyltransferase-deficient mice. Fourth, in common with LCAT-deficient mice, CAST mice contained triglyceride-rich lipoproteins with "panhandle"-like protrusions. To examine the genetic bases of these differences, we studied HDL lipid levels in an intercross between strain CAST and the common laboratory strain B6 on a low fat, chow diet as well as a high fat, atherogenic diet. HDL levels exhibited complex inheritance, as 12 quantitative trait loci with significant or suggestive likelihood of observed data scores were identified. Several of the loci occurred over plausible candidate genes and these were investigated.

The results indicate that the functional LCAT deficiency is unlikely to be due to variations of the LCAT gene. Our results suggest that novel genes are likely to be important in the control of HDL metabolism, and they provide evidence of genetic factors influencing the interaction of LCAT with HDL. Mehrabian, M., L. W. Castellani, P-Z. Wen, J. Wong, T. Rithaporn, S. Y. Hama, G. P. Hough, D. Johnson, J. J. Albers, G. A. Mottino, J. S. Frank, M. Navab, A. M. Fogelman, and A. J. Lusis. Genetic control of HDL levels and composition in an interspecific mouse cross (CAST/Ei x C57BL/6J). J. Lipid Res. 2000. 41: 1936;–1946.

Supplementary key words: quantitative trait locus mapping, lecithin:cholesterol acyltransferase, adrenal lipid depletion, scavenger receptor BI, phospholipid transfer protein, apolipoprotein A-I, cholesterol-7{alpha}-hydroxylase, high fat diet


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