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1 Universitat Autonoma de Barcelona
2 IRTA
3 Seleccion Batalle S.A.
4 Hospital de PalamOs
* To whom correspondence should be addressed. E-mail: raquel.quintanilla{at}irta.cat.
The fine mapping of polymorphisms influencing cholesterol, triglyceride and lipoprotein serum levels in human and mouse has provided a wealth of knowledge about the complex genetic architecture of these traits. The extension of these genetic analyses to pigs would be of outmost importance since they constitute a valuable biological and clinical model for the study of coronary artery disease and myocardial infarction. In the present work, we have performed a whole genome scan for serum lipid traits in a half-sib Duroc pig population of 350 individuals. Phenotypic registers included total cholesterol (CT), triglyceride (TG), and low (LDL) and high (HDL) density lipoprotein serum concentrations at 45 and 190 d of age. This approach allowed us to identify two genome-wide significant QTL for HDL/LDL ratio at 45 d (SSC6, 84 cM) and for TG at 190 d (SSC4, 23 cM) as well as a number of chromosome-wide significant QTL. The comparison of QTL locations at 45 d and 190 d revealed a notable lack of concordance at these two timepoints suggesting that the effects of these QTL are age-specific. Moreover, we have observed a considerable level of correspondence amongst the location of the most significant porcine lipid QTL and those identified in human. This finding might suggest that, in mammals, diverse polymorphisms located in a common set of genes are involved in the genetic variation of serum lipid levels.
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