Genetic control of lipids in the mouse cross DU6i x DBA/2

• Published in: Mammalian genome Vol. 18; no. 11; pp. 757 - 766
• Main Authors: Brockmann, Gudrun A, Karatayli, Ersin, Neuschl, Christina, Stylianou, Ioannis M, Aksu, Soner, Ludwig, Antje, Renne, Ulla, Haley, Chris S, Knott, Sara
• Format: Journal Article
• Language: English
• Published: United States New York : Springer-Verlag 01.11.2007
• Subjects: Animals; Cholesterol - blood; Cholesterol, HDL - blood; Cholesterol, LDL - blood; Chromosome Mapping; Crosses, Genetic; Epistasis, Genetic; Female; Genetic Markers; Lipids - blood; Lipids - genetics; Male; Mice; Mice, Inbred DBA; Mice, Inbred Strains; Quantitative Trait Loci; Sex Characteristics; Triglycerides - blood
• ISSN: 0938-8990; 1432-1777
• DOI: 10.1007/s00335-007-9068-7

An F₂ pedigree based on the mouse lines DU6i and DBA/2 with extremely different growth and obesity characteristics was generated to search for QTLs affecting serum concentrations of triglycerides (TG), total cholesterol (CHOL), HDL cholesterol (HDL-C), and LDL cholesterol (LDL-C). Compared with many other studies, we searched for spontaneous genetic variants contributing to high lipid levels under a standard breeding diet. Significant QTLs for CHOL were identified on chromosomes 4 and 6, and a female-specific locus on chromosome 3. QTLs for HDL-C were detected on chromosome 11 for both sexes, and on chromosome 1 for females. These QTLs are located in syntenic human regions that have QTLs that have not been previously confirmed in animal studies. LDL-C QTLs have been mapped for both sexes to chromosome 8 and in males on chromosome 13. Epistatic interactions that significantly accounted for the phenotypic variance of HDL-C, CHOL, and LDL-C serum concentrations were also detected with one interaction between chromosomes 8 and 15, accounting for 22% of the observed variance in LDL-C levels. The identified loci coincide in part with regions controlling growth and obesity. Thus, multiple genes or pleiotropic effects may be assumed. The identified QTLs for cholesterol and its transport proteins as subcomponents of risk for coronary heart disease will further improve our understanding of the genetic net controlling plasma lipid concentrations.