Literature DB >> 19436067

Four additional mouse crosses improve the lipid QTL landscape and identify Lipg as a QTL gene.

Zhiguang Su1, Naoki Ishimori, Yaoyu Chen, Edward H Leiter, Gary A Churchill, Beverly Paigen, Ioannis M Stylianou.   

Abstract

To identify genes controlling plasma HDL and triglyceride levels, quantitative trait locus (QTL) analysis was performed in one backcross, (NZO/H1Lt x NON/LtJ) x NON/LtJ, and three intercrosses, C57BL/6J x DBA/2J, C57BL/6J x C3H/HeJ, and NZB/B1NJ x NZW/LacJ. HDL concentrations were affected by 25 QTL distributed on most chromosomes (Chrs); those on Chrs 1, 8, 12, and 16 were newly identified, and the remainder were replications of previously identified QTL. Triglyceride concentrations were controlled by nine loci; those on Chrs 1, 2, 3, 7, 16, and 18 were newly identified QTL, and the remainder were replications. Combining mouse crosses with haplotype analysis for the HDL QTL on Chr 18 reduced the list of candidates to six genes. Further expression analysis, sequencing, and quantitative complementation testing of these six genes identified Lipg as the HDL QTL gene on distal Chr 18. The data from these crosses further increase the ability to perform haplotype analyses that can lead to the identification of causal lipid genes.

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Year:  2009        PMID: 19436067      PMCID: PMC2739753          DOI: 10.1194/jlr.M900076-JLR200

Source DB:  PubMed          Journal:  J Lipid Res        ISSN: 0022-2275            Impact factor:   5.922


  70 in total

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5.  Secondary prevention by raising HDL cholesterol and reducing triglycerides in patients with coronary artery disease.

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Journal:  J Clin Invest       Date:  2009-03-16       Impact factor: 14.808

Review 9.  Compendium of genome-wide scans of lipid-related phenotypes: adding a new genome-wide search of apolipoprotein levels.

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  27 in total

1.  Using bioinformatics and systems genetics to dissect HDL-cholesterol genetics in an MRL/MpJ x SM/J intercross.

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2.  Obesity-insulin targeted genes in the 3p26-25 region in human studies and LG/J and SM/J mice.

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Review 4.  HDL cholesterol and bone mineral density: is there a genetic link?

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5.  A comparative assessment of mandible shape in a consomic strain panel of the house mouse (Mus musculus)--implications for epistasis and evolvability of quantitative traits.

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6.  The mouse QTL map helps interpret human genome-wide association studies for HDL cholesterol.

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Review 8.  Genetic basis of atherosclerosis: insights from mice and humans.

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Review 9.  Genome-wide association studies in mice.

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10.  Novel ENU-induced point mutation in scavenger receptor class B, member 1, results in liver specific loss of SCARB1 protein.

Authors:  Ioannis M Stylianou; Karen L Svenson; Sara K VanOrman; Yanina Langle; John S Millar; Beverly Paigen; Daniel J Rader
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