Skip to main content
Log in

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

  • Published:
Mammalian Genome Aims and scope Submit manuscript

Abstract

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.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  • Anunciado RV, Nishimura M, Mori M, Ishikawa A, Tanaka S, et al. (2003) Quantitative trait locus analysis of serum insulin, triglyceride, total cholesterol and phospholipid levels in the (SM/J × A/J)F2 mice. Exp Anim 52:37–42

    Article  PubMed  CAS  Google Scholar 

  • Brockmann GA, Bevova MR (2002) Using mouse models to dissect the genetics of obesity. Trends Genet 18:367–376

    Article  PubMed  CAS  Google Scholar 

  • Brockmann GA, Haley CS, Renne U, Knott SA, Schwerin M (1998) Quantitative trait loci affecting body weight and fatness from a mouse line selected for extreme high growth. Genetics 150:369–381

    PubMed  CAS  Google Scholar 

  • Brockmann GA, Kratzsch J, Haley CS, Renne U, Schwerin M, et al. (2000) Single QTL effects, epistasis, and pleiotropy account for two-thirds of the phenotypic F(2) variance of growth and obesity in DU6i × DBA/2 mice. Genome Res 10:1941–1957

    Article  PubMed  CAS  Google Scholar 

  • Brockmann GA, Haley CS, Wolf E, Karle S, Kratzsch J, et al. (2001) Genome-wide search for loci controlling serum IGF binding protein levels of mice. FASEB J 15:978–987

    Article  PubMed  CAS  Google Scholar 

  • Bunger L, Laidlaw A, Bulfield G, Eisen EJ, Medrano JF, et al. (2001) Inbred lines of mice derived from long-term growth selected lines: unique resources for mapping growth genes. Mamm Genome 12:678–686

    Article  PubMed  CAS  Google Scholar 

  • Canizales-Quinteros S, Aguilar-Salinas CA, Reyes-Rodriguez E, Riba L, Rodriguez-Torres M, et al. (2003) Locus on chromosome 6p linked to elevated HDL cholesterol serum levels and to protection against premature atherosclerosis in a kindred with familial hypercholesterolemia. Circ Res 92:569–576

    Article  PubMed  CAS  Google Scholar 

  • Churchill GA, Doerge RW (1994) Empirical threshold values for quantitative trait mapping. Genetics 138:963–971

    PubMed  CAS  Google Scholar 

  • Despres JP (2006) Is visceral obesity the cause of the metabolic syndrome? Ann Med 38:52–63

    Article  PubMed  CAS  Google Scholar 

  • Expert Panel on Detection, Evaluation, Treatment of High Blood Cholesterol in Adults (2001) Executive Summary of the Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III). JAMA 285:2486–2497

    Article  Google Scholar 

  • Guyton AC, Hall JE (1996) Lipid metabolism. In: Textbook of medical physiology. 9th ed. WB Saunders Co., Philadelphia, pp 865–876

  • Haley CS, Knott SA, Elsen JM (1994) Mapping quantitative trait loci in crosses between outbred lines using least squares. Genetics 136:1195–1207

    PubMed  CAS  Google Scholar 

  • Knott SA, Haley CS (2000) Multitrait least squares for quantitative trait loci detection. Genetics 156:899–911

    PubMed  CAS  Google Scholar 

  • Korstanje R, Li R, Howard T, Kelmenson P, Marshall J, et al. (2004) Influence of sex and diet on quantitative trait loci for HDL cholesterol levels in an SM/J by NZB/BlNJ intercross population. J Lipid Res 45:881–888

    Article  PubMed  CAS  Google Scholar 

  • Lander E, Kruglyak L (1995) Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet 11:241–247

    Article  PubMed  CAS  Google Scholar 

  • Lilja HE, Suviolahti E, Soro-Paavonen A, Hiekkalinna T, Day A, et al. (2004) Locus for quantitative HDL-cholesterol on chromosome 10q in Finnish families with dyslipidemia. J Lipid Res 45:1876–1884

    Article  PubMed  CAS  Google Scholar 

  • Lusis AJ (2000) Atherosclerosis. Nature 407:233–241

    Article  PubMed  CAS  Google Scholar 

  • Nigam A, Bourassa MG, Fortier A, Guertin MC, Tardif JC (2006) The metabolic syndrome and its components and the long-term risk of death in patients with coronary heart disease. Am Heart J 151:514–521

    Article  PubMed  Google Scholar 

  • Park YW, Zhu S, Palaniappan L, Heshka S, Carnethon MR, et al. (2003) The metabolic syndrome: prevalence and associated risk factor findings in the US population from the Third National Health and Nutrition Examination Survey, 1988–1994. Arch Intern Med 163:427–436

    Article  PubMed  Google Scholar 

  • Peacock JM, Arnett DK, Atwood LD, Myers RH, Coon H, et al. (2001) Genome scan for quantitative trait loci linked to high-density lipoprotein cholesterol: The NHLBI Family Heart Study. Arterioscler Thromb Vasc Biol 21:1823–1828

    Article  PubMed  CAS  Google Scholar 

  • Rollins J, Chen Y, Paigen B, Wang X (2006) In search of new targets for plasma high-density lipoprotein cholesterol levels: promise of human-mouse comparative genomics. Trends Cardiovasc Med 16:220–234

    Article  PubMed  CAS  Google Scholar 

  • SAS Institute (1990) User’s guide: Statistics (Cary, NC: SAS Institute)

    Google Scholar 

  • Schüler L (1985) Mouse strain Fzt:Du and its use as model in animal breeding research. Arch Tierz 28:357–363

    Google Scholar 

  • Sen S, Churchill GA (2001) A statistical framework for quantitative trait mapping. Genetics 159:371–387

    PubMed  CAS  Google Scholar 

  • Sugiyama F, Churchill GA, Higgins DC, Johns C, Makaritsis KP, et al. (2001) Concordance of murine quantitative trait loci for salt-induced hypertension with rat and human loci. Genomics 71:70–77

    Article  PubMed  CAS  Google Scholar 

  • Svenson KL, Von Smith R, Magnani PA, Suetin HR, Paigen B, et al. (2007) Multiple trait measurements in 43 inbred mouse strains capture the phenotypic diversity characteristic of human populations. J Appl Physiol 102:2369–2378

    Article  PubMed  CAS  Google Scholar 

  • Valdar W, Solberg LC, Gauguier D, Burnett S, Klenerman P, et al. (2006) Genome-wide genetic association of complex traits in heterogeneous stock mice. Nat Genet 38:879–887

    Article  PubMed  CAS  Google Scholar 

  • Wang X, Paigen B (2002) Quantitative trait loci and candidate genes regulating HDL cholesterol: a murine chromosome map. Arterioscler Thromb Vasc Biol 22:1390–1401

    Article  PubMed  CAS  Google Scholar 

  • Wang X, Paigen B (2005a) Genetics of variation in HDL cholesterol in humans and mice. Circ Res 96:27–42

    Google Scholar 

  • Wang X, Paigen B (2005b) Genome-wide search for new genes controlling plasma lipid concentrations in mice and humans. Curr Opin Lipidol 16:127–137

    Google Scholar 

  • Wang X, Ishimori N, Korstanje R, Rollins J, Paigen B (2005) Identifying novel genes for atherosclerosis through mouse-human comparative genetics. Am J Hum Genet 77:1–15

    Article  PubMed  CAS  Google Scholar 

  • Welch CL, Bretschger S, Wen PZ, Mehrabian M, Latib N, et al. (2004) Novel QTLs for HDL levels identified in mice by controlling for Apoa2 allelic effects: confirmation of a chromosome 6 locus in a congenic strain. Physiol Genomics 17:48–59

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

Excellent technical assistance was provided by Hannelore Tychsen for DNA preparation and genotyping. We thank Jürgen Kratzsch from the Department of Clinical Chemistry and Pathobiochemistry at the University of Leipzig, and Beate Gomolka for their help in the evaluation of lipid measurements in mice. This work was supported by grants from the German Research Foundation (BR 1285/5), the German National Genome Research Network (NGFN2, registration no. 01GS0486), and the H. Wilhelm Schaumann Stiftung to GAB. CSH acknowledges support from the BBSRC and MAFF.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Gudrun A. Brockmann.

Electronic supplementary material

Rights and permissions

Reprints and permissions

About this article

Cite this article

Brockmann, G.A., Karatayli, E., Neuschl, C. et al. Genetic control of lipids in the mouse cross DU6i × DBA/2. Mamm Genome 18, 757–766 (2007). https://doi.org/10.1007/s00335-007-9068-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00335-007-9068-7

Keywords

Navigation