A systems genetic analysis of high density lipoprotein metabolism and network preservation across mouse models

被引:21
作者
Langfelder, Peter [1 ]
Castellani, Lawrence W. [2 ]
Zhou, Zhigiang [2 ]
Paul, Eric [2 ]
Davis, Richard [2 ]
Schadt, Eric E. [4 ]
Lusis, Aldons J. [1 ,2 ,3 ]
Horvath, Steve [1 ,5 ]
Mehrabian, Margarete [2 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Gonda Goldschmied Neurosci & Genet Res Ctr, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Div Cardiol, Los Angeles, CA 90095 USA
[3] Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
[4] Pacific Biosci, Menlo Pk, CA 94025 USA
[5] Univ Calif Los Angeles, David Geffen Sch Med, Dept Biostat, Los Angeles, CA 90095 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 2012年 / 1821卷 / 03期
基金
美国国家卫生研究院;
关键词
HDL; Genetics; Network; Co-expression; HDL CHOLESTEROL; ANTIINFLAMMATORY PROPERTIES; ATHEROSCLEROTIC LESIONS; TRANSGENIC MICE; LOCI; PLASMA; EXPRESSION; IDENTIFICATION; MECHANISM; CELLS;
D O I
10.1016/j.bbalip.2011.07.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We report a systems genetic analysis of high density lipoprotein (HDL) levels in an F2 intercross between inbred strains CAST/EiJ and C57BL/6J. We previously showed that there are dramatic differences in HDL metabolism in a cross between these strains, and we now report co-expression network analysis of HDL that integrates global expression data from liver and adipose with relevant metabolic traits. Using data from a total of 293 F2 intercross mice, we constructed weighted gene co-expression networks and identified modules (subnetworks) associated with HDL and clinical traits. These were examined for genes implicated in HDL levels based on large human genome-wide associations studies (GWAS) and examined with respect to conservation between tissue and sexes in a total of 9 data sets. We identify genes that are consistently ranked high by association with HDL across the 9 data sets. We focus in particular on two genes, Wfdc2 and Hdac3, that are located in close proximity to HDL QTL peaks where causal testing indicates that they may affect HDL Our results provide a rich resource for studies of complex metabolic interactions involving HDL. This article is part of a Special Issue entitled Advances in High Density Lipoprotein Formation and Metabolism: A Tribute to John F. Oram (1945-2010). (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:435 / 447
页数:13
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