4.5 Article

Mapping of quantitative trait loci for cholesterol, LDL, HDL, and triglyceride serum concentrations in pigs

期刊

PHYSIOLOGICAL GENOMICS
卷 35, 期 3, 页码 199-209

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/physiolgenomics.90249.2008

关键词

lipoproteins; lipid metabolism; candidate genes

资金

  1. Ministerio de Educacion y Ciencia, Spain [AGL2002-04271-C03, AGL200766707-C02]
  2. Universitat Autonoma de Barcelona
  3. Instituto Nacional de Investigacion Agropecuaria (Spain)

向作者/读者索取更多资源

Gallardo D, Pena RN, Amills M, Varona L, Ramirez O, Reixach J, Diaz I, Tibau J, Soler J, Prat-Cuffi JM, Noguera JL, Quintanilla R. Mapping of quantitative trait loci for cholesterol, LDL, HDL and triglyceride serum concentrations in pigs. Physiol Genomics 35: 199-209, 2008. First published September 23, 2008; doi: 10.1152/physiolgenomics.90249.2008.-The fine mapping of polymorphisms influencing cholesterol (CT), triglyceride (TG), 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 utmost 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 performed a whole genome scan for serum lipid traits in a half-sib Duroc pig population of 350 individuals. Phenotypic registers included total CT, TG, and low (LDL)- and high (HDL)-density lipoprotein serum concentrations at 45 and 190 days of age. This approach allowed us to identify two genomewide significant quantitative trait loci (QTL) for HDL-to-LDL ratio at 45 days (SSC6, 84 cM) and for TG at 190 days (SSC4, 23 cM) as well as a number of chromosomewide significant QTL. The comparison of QTL locations at 45 and 190 days revealed a notable lack of concordance at these two time points, suggesting that the effects of these QTL are age specific. Moreover, we have observed a considerable level of correspondence among the locations of the most significant porcine lipid QTL and those identified in humans. 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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