罕见的低频编码变体改变人类的成年身高
Eirini Marouli1, Mariaelisa Graff2, Carolina Medina-Gomez3,4
1William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London EC1M 6BQ, UK.
Nature
|February 2, 2017
概括
研究人员发现了83种罕见的基因变异, 显著影响人类的身高, 其中一些高达2厘米. 这些发现揭示了影响生长的新生物学途径,并证明了大规模遗传研究的力量.
科学领域:
- 人类遗传学
- 分子生物学
- 生物化学
背景情况:
- 人的身高是一个复杂的多基因特征,受众共同的遗传变异的影响.
- 之前的全基因组关联研究 (GWAS) 已经确定了大约700种与身高相关的常见变异.
研究的目的:
- 确定对人类身高有重大影响的罕见和低频基因变异.
- 调查身高变化背后的功能机制和生物学途径.
主要方法:
- 进行了大规模的全基因组关联研究 (GWAS),以确定与身高相关的变异.
- 进行了功能后续研究,包括体外实验,以阐明特定变体的影响.
主要成果:
- 发现了83种与身高相关的编码变异,其小等位基因频率在0. 1- 4. 8%之间.
- 通过影响胰岛素类生长因子的生物可用性,几种变体,特别是STC2,对身高产生了很大的影响 (每种1 - 2厘米).
- 这些变异与涉及单一生长障碍的基因重叠,突出显示新型基因 (例如ADAMTS3,IL11RA,NOX4) 和途径 (例如蛋白质糖合成).
结论:
- 大型样本可以发现罕见的低频变异,对高度等多基因特征产生中等到大效应.
- 这些变体为人类生长的遗传结构提供了洞察力,并为与生长相关的研究确定了新的生物目标.
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