Genetic Architecture of Complex Human Traits: What Have We Learned from Genome-Wide Association Studies?

被引:0
作者
Ge Zhang
机构
[1] Cincinnati Children’s Hospital Medical Center,Human Genetics Division
关键词
Complex trait; Genetic architecture; Genome-wide association study; Heritability; Pleiotropy; Epistasis;
D O I
10.1007/s40142-015-0083-9
中图分类号
学科分类号
摘要
Genome-wide association studies have identified thousands of genetic variants associated with various complex human traits and diseases. These results opened a window to the genetic architecture of complex human traits. The fact that the identified variants usually confer small effects and explain only a small fraction of heritability has led the discussion of where to find the ‘missing heritability.’ Two competitive models have been proposed: the ‘infinitesimal model’ suggests large number of variants of small effects and the ‘rare variant model’ suggests multiple large-effect rare variants. Recent empirical studies and theoretical analyses suggest that the infinitesimal model might dominate the true genetic architecture of most complex traits. Large-effect rare variants may exist and might be functionally important but contribute little to heritability.
引用
收藏
页码:143 / 150
页数:7
相关论文
共 465 条
[1]  
Mackay TF(2001)The genetic architecture of quantitative traits Annu Rev Genet 35 303-339
[2]  
Hansen TF(2006)The evolution of genetic architecture Annu Rev Ecol Evol Syst 37 123-157
[3]  
Hindorff LA(2009)Potential etiologic and functional implications of genome-wide association loci for human diseases and traits Proc Natl Acad Sci USA 106 9362-9367
[4]  
Sethupathy P(2014)The NHGRI GWAS Catalog, a curated resource of SNP-trait associations Nucleic Acids Res. 42 D1001-D1006
[5]  
Junkins HA(2011)Progress and promise of genome-wide association studies for human complex trait genetics Genetics 187 367-383
[6]  
Ramos EM(2012)Five years of GWAS discovery Am J Hum Genet 90 7-24
[7]  
Mehta JP(1999)Population genetics–making sense out of sequence Nat Genet 21 56-60
[8]  
Collins FS(2001)On the allelic spectrum of human disease Trends Genet 17 502-510
[9]  
Welter D(2009)Finding the missing heritability of complex diseases Nature 461 747-753
[10]  
MacArthur J(2010)Missing heritability and strategies for finding the underlying causes of complex disease Nat Rev Genet 11 446-450