描述成年表观遗传钟部位的发育动态
Rosa H Mulder1, Alexander Neumann1, Janine F Felix2
1Department of Child and Adolescent Psychiatry/Psychology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands; The Generation R Study Group, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.
基于DNA甲基化的表观遗传时钟,从出生开始显示出显著的个体差异. 这些变异受到遗传学和产前因素的影响,这表明衰老过程的早期起源.
科学领域:
- 表观遗传学和衰老生物学
背景情况:
- 基因甲基化 (DNAm) 调节基因活动,并随着年龄的增长而发生变化.
- 从DNAm网站获得的表观遗传时钟是生物年龄的生物标志物.
- 了解时钟位置的早期生命变异性对于促进健康衰老至关重要.
研究的目的:
- 描述表观遗传钟位点的发育轨迹,从出生到成年早期.
- 在早期发展过程中确定影响时钟位置的个体差异的因素.
主要方法:
- 分析了来自两个基于人口的队列的纵向数据 (N=5019个样本,2348个人).
- 检查了成人时钟站点的轨迹,从出生到成年早期.
- 用全表观基因组关联元分析测试了基因和产前暴露的丰富性.
主要成果:
- 时钟站点表现出多样化,往往非线性,发展轨迹.
- 时钟位置的个体差异从出生就存在,并预测了以后的变化.
- 时钟位置对遗传影响和产前暴露 (例如吸烟,饮食,孕产妇健康) 进行了丰富.
结论:
- 与年龄相关的表观遗传过程可能在发育早期产生和分离.
- 了解表观遗传变异的早期驱动因素,可以为健康老龄化策略提供信息.
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