Integration of QTL and bioinformatic tools to identify candidate genes for triglycerides in mice

被引:22
作者
Leduc, Magalie S. [2 ]
Hageman, Rachael S. [1 ]
Verdugo, Ricardo A. [1 ]
Tsaih, Shirng-Wern [3 ]
Walsh, Kenneth [1 ]
Churchill, Gary A. [1 ]
Paigen, Beverly [1 ]
机构
[1] Jackson Lab, Bar Harbor, ME 04609 USA
[2] Texas Biomed Res Inst, San Antonio, TX USA
[3] Med Coll Wisconsin, Human & Mol Genet Ctr, Milwaukee, WI 53226 USA
基金
美国国家卫生研究院;
关键词
quantitative trait loci; gene expression; genetics; QUANTITATIVE TRAIT LOCI; SUSCEPTIBILITY GENE; CHOLESTEROL LEVELS; LABORATORY MOUSE; HDL CHOLESTEROL; EXPRESSION; IDENTIFICATION; INTERCROSS; POPULATION; STRAINS;
D O I
10.1194/jlr.M011130
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
To identify genetic loci influencing lipid levels, we performed quantitative trait loci (QTL) analysis between inbred mouse strains MRL/MpJ and SM/J, measuring triglyceride levels at 8 weeks of age in F2 mice fed a chow diet. We identified one significant QTL on chromosome (Chr) 15 and three suggestive QTL on Chrs 2, 7, and 17. We also carried out microarray analysis on the livers of parental strains of 282 F2 mice and used these data to find cis-regulated expression QTL. We then narrowed the list of candidate genes under significant QTL using a "toolbox" of bioinformatic resources, including haplotype analysis; parental strain comparison for gene expression differences and nonsynonymous coding single nucleotide polymorphisms (SNP); cis-regulated eQTL in livers of F2 mice; correlation between gene expression and phenotype; and conditioning of expression on the phenotype. We suggest Slc25a7 as a candidate gene for the Chr 7 QTL and, based on expression differences, five genes (Polr3 h, Cyp2d22, Cyp2d26, Tspo, and Ttll12) as candidate genes for Chr 15 QTL. This study shows how bioinformatics can be used effectively to reduce candidate gene lists for QTL related to complex traits.-Leduc, M. S., R. S. Hageman, R. A. Verdugo, S-W. Tsaih, K. Walsh, G. A. Churchill, and B. Paigen. Integration of QTL and bioinformatic tools to identify candidate genes for triglycerides in mice. J. Lipid Res. 2011. 52: 1672-1682.
引用
收藏
页码:1672 / 1682
页数:11
相关论文
共 44 条
[1]   The nature and identification of quantitative trait loci: a community's view [J].
Abiola, O ;
Angel, JM ;
Avner, P ;
Bachmanov, AA ;
Belknap, JK ;
Bennett, B ;
Blankenhorn, EP ;
Blizard, DA ;
Bolivar, V ;
Brockmann, GA ;
Buck, KJ ;
Bureau, JF ;
Casley, WL ;
Chesler, EJ ;
Cheverud, JM ;
Churchill, GA ;
Cook, M ;
Crabbe, JC ;
Crusio, WE ;
Darvasi, A ;
de Haan, G ;
Demant, P ;
Doerge, RW ;
Elliott, RW ;
Farber, CR ;
Flaherty, L ;
Flint, J ;
Gershenfeld, H ;
Gu, JPGJ ;
Gu, WK ;
Himmelbauer, H ;
Hitzemann, R ;
Hsu, HC ;
Hunter, K ;
Iraqi, FA ;
Jansen, RC ;
Johnson, TE ;
Jones, BC ;
Kempermann, G ;
Lammert, F ;
Lu, L ;
Manly, KF ;
Matthews, DB ;
Medrano, JF ;
Mehrabian, M ;
Mittleman, G ;
Mock, BA ;
Mogil, JS ;
Montagutelli, X ;
Morahan, G .
NATURE REVIEWS GENETICS, 2003, 4 (11) :911-916
[2]   Sex Specific Gene Regulation and Expression QTLs in Mouse Macrophages from a Strain Intercross [J].
Bhasin, Jeffrey M. ;
Chakrabarti, Enakshi ;
Peng, Dao-Quan ;
Kulkarni, Aneesh ;
Chen, Xi ;
Smith, Jonathan D. .
PLOS ONE, 2008, 3 (01)
[3]   A comparison of normalization methods for high density oligonucleotide array data based on variance and bias [J].
Bolstad, BM ;
Irizarry, RA ;
Åstrand, M ;
Speed, TP .
BIOINFORMATICS, 2003, 19 (02) :185-193
[4]   The X chromosome in quantitative trait locus mapping [J].
Broman, Karl W. ;
Sen, Saunak ;
Owens, Sarah E. ;
Manichaikul, Ani ;
Southard-Smith, E. Michelle ;
Churchill, Gary A. .
GENETICS, 2006, 174 (04) :2151-2158
[5]  
Broman KW, 2009, STAT BIOL HEALTH, P1, DOI 10.1007/978-0-387-92125-9_1
[6]   R/qtl: QTL mapping in experimental crosses [J].
Broman, KW ;
Wu, H ;
Sen, S ;
Churchill, GA .
BIOINFORMATICS, 2003, 19 (07) :889-890
[7]   Practical Applications of the Bioinformatics Toolbox for Narrowing Quantitative Trait Loci [J].
Burgess-Herbert, Sarah L. ;
Cox, Allison ;
Tsaih, Shirng-Wern ;
Paigen, Beverly .
GENETICS, 2008, 180 (04) :2227-2235
[8]   HDL CHOLESTEROL AND OTHER LIPIDS IN CORONARY HEART-DISEASE - COOPERATIVE LIPOPROTEIN PHENOTYPING STUDY [J].
CASTELLI, WP ;
DOYLE, JT ;
GORDON, T ;
HAMES, CG ;
HJORTLAND, MC ;
HULLEY, SB ;
KAGAN, A ;
ZUKEL, WJ .
CIRCULATION, 1977, 55 (05) :767-772
[9]   Integrating QTL and high-density SNP analyses in mice to identify Insig2 as a susceptibility gene for plasma cholesterol levels [J].
Cervino, AC ;
Li, GY ;
Edwards, S ;
Zhu, J ;
Laurie, C ;
Tokiwa, G ;
Lum, PY ;
Wang, S ;
Castellini, LW ;
Lusis, AJ ;
Carlson, S ;
Sachs, AB ;
Schadt, EE .
GENOMICS, 2005, 86 (05) :505-517
[10]   A New Standard Genetic Map for the Laboratory Mouse [J].
Cox, Allison ;
Ackert-Bicknell, Cheryl L. ;
Dumont, Beth L. ;
Ding, Yueming ;
Bell, Jordana Tzenova ;
Brockmann, Gudrun A. ;
Wergedal, Jon E. ;
Bult, Carol ;
Paigen, Beverly ;
Flint, Jonathan ;
Tsaih, Shirng-Wern ;
Churchill, Gary A. ;
Broman, Karl W. .
GENETICS, 2009, 182 (04) :1335-1344