J. Lipid Res.
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A more recent version of this article appeared on September 1, 2003

Papers In Press, published online ahead of print June 16, 2003
J. Lipid Res., doi:10.1194/jlr.M300139-JLR200
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Submitted on April 2, 2003
Revised on May 27, 2003
Accepted on June 5, 2003

Loci controlling plasma non-HDL and HDL cholesterol levels in a C57BL/6J X CASA/Rk intercross

Ephraim Sehayek, Elizabeth M. Duncan, Hannah J. Yu, Lynn Petukhova, and Jan L. Breslow

Laboratory of Biochemical Genetics and Metabolism, The Rockefeller University, New York, NY 10021

Corresponding Author: sehayee{at}rockefeller.edu

Plasma non-HDL and HDL cholesterol levels are predictors of cardiovascular diseases. We carried out a genetic cross between two laboratory inbred mouse strains, C57BL/6J and CASA/Rk, to detect loci that control the plasma levels of non-HDL and HDL cholesterol. With regard to non-HDL cholesterol, chow fed CASA/Rk males and females had 87% and 25% higher levels, respectively, than C57BL/6Js. The levels of non-HDL cholesterol in F1s were similar to C57BL/6J. There was no strain difference in HDL cholesterol levels. An intercross between F1s was performed and plasma non-HDL and HDL cholesterol measured in 185 male and 184 female mice. In both F2 males and females, plasma non-HDL and HDL cholesterol levels were unimodally distributed; however, in both cases the values for females were significantly lower than for males. Therefore, linkage analysis was performed with sex as a covariate. Significant linkage for non-HDL cholesterol was found on chromosome 6 at 49 cM (LOD 5.17), chromosome 4 at 55 cM (LOD 4.22), and chromosome 8 at 7 cM (LOD 3.68). Significant linkage for HDL cholesterol was found on chromosome 9 at 14 cM (LOD 7.52) and chromosome 8 at 76 cM (LOD 4.69). A significant epistatic interaction, involving loci on chromosomes 2 and 5, was also observed for non-HDL cholesterol. In summary, linkage analysis in this cross identified novel loci, confirmed previously identified loci in control of plasma non-HDL and HDL cholesterol and disclosed a novel interaction in controlling non-HDL cholesterol levels in the mouse.


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