Population genomics of human gene expression

被引:886
作者
Stranger, Barbara E.
Nica, Alexandra C.
Forrest, Matthew S.
Dimas, Antigone
Bird, Christine P.
Beazley, Claude
Ingle, Catherine E.
Dunning, Mark
Flicek, Paul
Koller, Daphne
Montgomery, Stephen
Tavare, Simon
Deloukas, Panos
Dermitzakis, Emmanouil T.
机构
[1] Wellcome Trust Sanger Inst, Cambridge CB10 1SA, England
[2] Univ Cambridge, Li Ka Shing Ctr, Canc Res UK Cambridge Res Inst, Dept Oncol, Cambridge CB2 0RE, England
[3] Stanford Univ, Dept Comp Sci, Stanford, CA 94305 USA
基金
英国惠康基金;
关键词
D O I
10.1038/ng2142
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genetic variation influences gene expression, and this variation in gene expression can be efficiently mapped to specific genomic regions and variants. Here we have used gene expression profiling of Epstein-Barr virus-transformed lymphoblastoid cell lines of all 270 individuals genotyped in the HapMap Consortium to elucidate the detailed features of genetic variation underlying gene expression variation. We find that gene expression is heritable and that differentiation between populations is in agreement with earlier small-scale studies. A detailed association analysis of over 2.2 million common SNPs per population ( 5% frequency in HapMap) with gene expression identified at least 1,348 genes with association signals in cis and at least 180 in trans. Replication in at least one independent population was achieved for 37% of cis signals and 15% of trans signals, respectively. Our results strongly support an abundance of cis-regulatory variation in the human genome. Detection of trans effects is limited but suggests that regulatory variation may be the key primary effect contributing to phenotypic variation in humans. We also explore several methodologies that improve the current state of analysis of gene expression variation.
引用
收藏
页码:1217 / 1224
页数:8
相关论文
共 43 条
[21]   Functional analysis of polymorphisms in the promoter regions of genes on 22q11 [J].
Hoogendoorn, B ;
Coleman, SL ;
Guy, CA ;
Smith, SK ;
O'Donovan, MC ;
Buckland, PR .
HUMAN MUTATION, 2004, 24 (01) :35-42
[22]  
*INT HAPMAP CONS, IN PRESS NATURE
[23]   Long-range control of gene expression: Emerging mechanisms and disruption in disease [J].
Kleinjan, DA ;
van Heyningen, V .
AMERICAN JOURNAL OF HUMAN GENETICS, 2005, 76 (01) :8-32
[24]   Regulatory polymorphisms underlying complex disease traits [J].
Knight, JC .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2005, 83 (02) :97-109
[25]  
KOREAN M, 2006, BRIT J CANCER, V94, P1539
[26]   A novel, high-performance random array platform for quantitative gene expression profiling [J].
Kuhn, K ;
Baker, SC ;
Chudin, E ;
Lieu, MH ;
Oeser, S ;
Bennett, H ;
Rigault, P ;
Barker, D ;
McDaniel, TK ;
Chee, MS .
GENOME RESEARCH, 2004, 14 (11) :2347-2356
[27]   Identifying regulatory mechanisms using individual variation reveals key role for chromatin modification [J].
Lee, Su-In ;
Pe'ert, Dana ;
Dudley, Aimee M. ;
Church, George M. ;
Koller, Daphne .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (38) :14062-14067
[28]   CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration [J].
Li, Mingyao ;
Atmaca-Sonmez, Pelin ;
Othman, Mohammad ;
Branham, Kari E. H. ;
Khanna, Ritu ;
Wade, Michael S. ;
Li, Yun ;
Liang, Liming ;
Zareparsi, Sepideh ;
Swaroop, Anand ;
Abecasis, Goncalo R. .
NATURE GENETICS, 2006, 38 (09) :1049-1054
[29]   Apolipoprotein E: from atherosclerosis to Alzheimer's disease and beyond [J].
Mahley, RW ;
Huang, YD .
CURRENT OPINION IN LIPIDOLOGY, 1999, 10 (03) :207-217
[30]   Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes [J].
Merla, Giuseppe ;
Howald, Cedric ;
Henrichsen, Charlotte N. ;
Lyle, Robert ;
Wyss, Carine ;
Zabot, Marie-Therese ;
Antonarakis, Stylianos E. ;
Reymond, Alexandre .
AMERICAN JOURNAL OF HUMAN GENETICS, 2006, 79 (02) :332-341