Cis-acting expression quantitative trait loci in mice

被引:216
作者
Doss, S
Schadt, EE
Drake, TA
Lusis, AJ [1 ]
机构
[1] Univ Calif Los Angeles, Dept Human Genet, David Geffen Sch Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Microbiol Immunol & Mol Genet, David Geffen Sch Med, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Dept Pathol & Lab Med, David Geffen Sch Med, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Dept Med, David Geffen Sch Med, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90095 USA
[6] Rosetta Inpharmat, Kirkland, WA 98034 USA
关键词
D O I
10.1101/gr.3216905
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 previously reported the analysis of genome-wide expression profiles and various diabetes-related traits in a segregating cross between inbred mouse strains C57BL/6J (B6) and DBA/2J (DBA). By considering transcript levels as quantitative traits, we identified several thousand expression quantitative trait loci [eQTL] with LOD score > 4.3. We now experimentally address the problem of multiple comparisons by estimating the fraction of false-positive eQTL that are Under cis-acting regulation. For this, we have Utilized a classic cis-trans test with (B6 x DBA)F-1 rilice to determine the relative levels of transcripts from the B6 and DBA alleles. The results suggest that at least 64% of cis-acting eQTL with LOD > 4.3 are true Positives, while the remaining, 36% could not be confirmed as truly cis-acting. Moreover, we find that > 96% of apparent cis-acting eQTL occur ill regions that do not share SNP haplotypes. Cis-acting eQTL serve as ail important new resource for the identification of positional candidates ill QTL studies ill mice. Also, we Use the analysis of the correlation structures between genotypes, gene expression traits, and phenotypic traits to further characterize genes expressed ill liver that are Under cis-acting control, and highlight the advantages and disadvantages of integrating genetics and gene expression data in segregating populations.
引用
收藏
页码:681 / 691
页数:11
相关论文
共 26 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]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[3]   Genetic dissection of transcriptional regulation in budding yeast [J].
Brem, RB ;
Yvert, G ;
Clinton, R ;
Kruglyak, L .
SCIENCE, 2002, 296 (5568) :752-755
[4]   Genetic correlates of gene expression in recombinant inbred strains - A relational model system to explore neurobehavioral phenotypes [J].
Chesler, EJ ;
Wang, JT ;
Lu, L ;
Qu, YH ;
Manly, KF ;
Williams, RW .
NEUROINFORMATICS, 2003, 1 (04) :343-357
[5]   Genetic loci for diet-induced atherosclerotic lesions and plasma lipids in mice [J].
Colinayo, VV ;
Qiao, JH ;
Wang, XP ;
Krass, KL ;
Schadt, E ;
Lusis, AJ ;
Drake, TA .
MAMMALIAN GENOME, 2003, 14 (07) :464-471
[6]   Detection of regulatory variation in mouse genes [J].
Cowles, CR ;
Hirschhorn, JN ;
Altshuler, D ;
Lander, ES .
NATURE GENETICS, 2002, 32 (03) :432-437
[7]   Genetic loci determining bone density in mice with diet-induced atherosclerosis [J].
Drake, TA ;
Schadt, E ;
Hannani, K ;
Kabo, JM ;
Krass, K ;
Colinayo, V ;
Greaser, LE ;
Goldin, J ;
Lusis, AJ .
PHYSIOLOGICAL GENOMICS, 2001, 5 (04) :205-215
[8]   Finding the molecular basis of quantitative traits: Successes and pitfalls [J].
Flint, J ;
Mott, R .
NATURE REVIEWS GENETICS, 2001, 2 (06) :437-445
[9]   cDNA expression arrays reveal incomplete reversal of age-related changes in gene expression by calorie restriction [J].
Han, ES ;
Hilsenbeck, SG ;
Richardson, A ;
Nelson, JF .
MECHANISMS OF AGEING AND DEVELOPMENT, 2000, 115 (03) :157-174
[10]   Microarray standard data set and figures of merit for comparing data processing methods and experiment designs [J].
He, YDD ;
Dai, HY ;
Schadt, EE ;
Cavet, G ;
Edwards, SW ;
Stepaniants, SB ;
Duenwald, S ;
Kleinhanz, R ;
Jones, AR ;
Shoemaker, DD ;
Stoughton, RB .
BIOINFORMATICS, 2003, 19 (08) :956-965