Ancient selection for derived alleles at a GDF5 enhancer influencing human growth and osteoarthritis risk

被引:74
作者
Capellini, Terence D. [1 ,2 ]
Chen, Hao [2 ,6 ]
Cao, Jiaxue [1 ,7 ]
Doxey, Andrew C. [3 ]
Kiapour, Ata M. [4 ]
Schoor, Michael [2 ,8 ]
Kingsley, David M. [2 ,5 ]
机构
[1] Harvard Univ, Human Evolutionary Biol, Cambridge, MA 02138 USA
[2] Stanford Univ, Dept Dev Biol, Stanford, CA 94305 USA
[3] Univ Waterloo, Dept Biol, Waterloo, ON, Canada
[4] Harvard Med Sch, Boston Childrens Hosp, Dept Orthoped Surg, Boston, MA USA
[5] Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA
[6] Genentech Inc, San Francisco, CA USA
[7] Sichuan Agr Univ, Farm Anim Genet Resources Explorat & Innovat Key, Chengdu, Sichuan, Peoples R China
[8] Miltenyi Biotec, Bergisch Gladbach, Germany
基金
加拿大自然科学与工程研究理事会;
关键词
BINDING MICROARRAY DATA; HIP AXIS LENGTH; POSITIVE SELECTION; GENOME SEQUENCE; ONLINE DATABASE; VARIANTS; ASSOCIATION; MUTATIONS; SUSCEPTIBILITY; POLYMORPHISM;
D O I
10.1038/ng.3911
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Variants in GDF5 are associated with human arthritis and decreased height, but the causal mutations are still unknown. We surveyed the Gdf5 locus for regulatory regions in transgenic mice and fine-mapped separate enhancers controlling expression in joints versus growing ends of long bones. A large downstream regulatory region contains a novel growth enhancer (GROW1), which is required for normal Gdf5 expression at ends of developing bones and for normal bone lengths in vivo. Human GROW1 contains a common base-pair change that decreases enhancer activity and colocalizes with peaks of positive selection in humans. The derived allele is rare in Africa but common in Eurasia and is found in Neandertals and Denisovans. Our results suggest that an ancient regulatory variant in GROW1 has been repeatedly selected in northern environments and that past selection on growth phenotypes explains the high frequency of a GDF5 haplotype that also increases arthritis susceptibility in many human populations.
引用
收藏
页码:1202 / +
页数:13
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