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Published Online
on December 22, 2005

Arteriosclerosis, Thrombosis, and Vascular Biology. 2005
Published online before print December 22, 2005, doi: 10.1161/01.ATV.0000201044.33220.5c
A more recent version of this article appeared on March 1, 2006
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Submitted on October 5, 2005
Accepted on December 7, 2005

Atherosclerosis Susceptibility Loci Identified From a Strain Intercross of Apolipoprotein E-Deficient Mice via a High-Density Genome Scan

Jonathan D. Smith *; Jeffrey M. Bhasin ; Julie Baglione ; Megan Settle ; Yaomin Xu ; and John Barnard

From the Departments of Cell Biology (J.D.S., J.M.B., J.B., M.S.), Cardiovascular Medicine (J.D.S.), and Quantitative Health Sciences (Y.X., J.Barnard), Cleveland Clinic Foundation, Cleveland Ohio; and the Department of Molecular Medicine (J.D.S.), Case School of Medicine, Cleveland Ohio.

* To whom correspondence should be addressed. E-mail: smithj4{at}ccf.org.

Objective--Apolipoprotein (apo) E-deficient mice are hypercholesterolemic and develop atherosclerosis on low-fat chow diets; however, the genetic background strain has a large effect on atherosclerosis susceptibility. This study aimed to determine the genetic regions associated with strain effects on lesion area.

Methods and Results--We performed a strain intercross between atherosclerosis sensitive DBA/2 and atherosclerosis resistant AKR apoE-deficient mice. Aortic root lesion area, total cholesterol, body weights, and complete blood counts were ascertained for 114 male and 95 female F2 progeny. A high-density genome scan was performed using a mouse single nucleotide polymorphism chip yielding 1967 informative polymorphic markers. Quantitative trait locus (QTL) statistical analyses were performed. Novel loci associated with lesion or log lesion area were identified for the female and male F2 cohorts. The atherosclerosis QTLs in female mice reside on chromosomes 15, 5, 3, and 13, and in male mice on chromosomes 17, 18, and 2. QTL were also identified for body weight, total cholesterol, and blood count parameters.

Conclusions--Loci were identified for atherosclerosis susceptibility in a strain intercross study. The identity of the responsible genes at these loci remains to be determined.


Key words: atherosclerosis • mouse genetics • quantitative trait locus • QTL




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