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在一个影响人类生长和骨关节炎风险的GDF5增强子上对衍生等位基因的古代选择。

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

作者信息

Capellini Terence D, Chen Hao, Cao Jiaxue, Doxey Andrew C, Kiapour Ata M, Schoor Michael, Kingsley David M

机构信息

Human Evolutionary Biology, Harvard University, Cambridge, Massachusetts, USA.

Department of Developmental Biology, Stanford University, Stanford, California, USA.

出版信息

Nat Genet. 2017 Aug;49(8):1202-1210. doi: 10.1038/ng.3911. Epub 2017 Jul 3.

Abstract

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.

摘要

生长分化因子5(GDF5)的变异与人类关节炎和身高降低有关,但致病突变仍不清楚。我们在转基因小鼠中研究了Gdf5基因座的调控区域,并精细定位了分别控制关节和长骨生长末端表达的增强子。一个大的下游调控区域包含一个新的生长增强子(GROW1),它是发育中骨骼末端正常Gdf5表达和体内正常骨长度所必需的。人类GROW1包含一个常见的碱基对变化,该变化会降低增强子活性,并与人类正选择峰共定位。衍生等位基因在非洲很少见,但在欧亚大陆很常见,并且在尼安德特人和丹尼索瓦人中也有发现。我们的结果表明,GROW1中的一个古老调控变异在北方环境中被反复选择,过去对生长表型的选择解释了GDF5单倍型的高频率,该单倍型在许多人类群体中也增加了关节炎易感性。

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