神经发育障碍中的调节元件的新突变
Patrick J Short1, Jeremy F McRae1, Giuseppe Gallone1
1Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, UK.
Nature
|March 22, 2018
概括
调节元件的新突变,特别是胎儿大脑活性区域,是神经发育障碍的重要原因. 这项研究估计了它们在缺乏编码变异的患者中的贡献.
科学领域:
- 遗传学
- 发育生物学
- 基因组监管
背景情况:
- 以前,42%的严重发育障碍病例与代码序列的新突变有关.
- 在监管要素中新突变的作用仍然在很大程度上未被探索.
- 调控因素控制基因表达,对发育至关重要.
研究的目的:
- 调查调控元素中新突变对发育障碍的影响.
- 在受影响的个体中识别特定类型的调控元素.
- 估计这些突变在神经发育障碍中的流行程度和影响.
主要方法:
- 在近8000名患者中分析了三类假定调节元件的新突变.
- 进化保存和功能活动的评估 (胎儿大脑活性元素).
- 统计分析以确定缩和估计突变率.
主要成果:
- 在高度保存的胎儿大脑活性元素中的新突变在神经发育障碍中显著丰富.
- 观察到经常发生突变的元素的双重丰富.
- 据估计,在没有编码变异的患者中,有1-3%携带这些调节元件的新发病性突变.
结论:
- 调节元件的新突变,特别是保存的胎儿大脑活性的突变,是神经发育障碍的重要遗传原因.
- 这一发现扩大了对编码区域之外的遗传基础的理解.
- 结合功能和进化数据对于识别遗传疾病的调节原因至关重要.
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