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DNA 甲基化衰老钟:挑战与建议。

DNA methylation aging clocks: challenges and recommendations.

机构信息

William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.

The Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.

出版信息

Genome Biol. 2019 Nov 25;20(1):249. doi: 10.1186/s13059-019-1824-y.

Abstract

Epigenetic clocks comprise a set of CpG sites whose DNA methylation levels measure subject age. These clocks are acknowledged as a highly accurate molecular correlate of chronological age in humans and other vertebrates. Also, extensive research is aimed at their potential to quantify biological aging rates and test longevity or rejuvenating interventions. Here, we discuss key challenges to understand clock mechanisms and biomarker utility. This requires dissecting the drivers and regulators of age-related changes in single-cell, tissue- and disease-specific models, as well as exploring other epigenomic marks, longitudinal and diverse population studies, and non-human models. We also highlight important ethical issues in forensic age determination and predicting the trajectory of biological aging in an individual.

摘要

表观遗传钟由一组 CpG 位点组成,其 DNA 甲基化水平可衡量受检者的年龄。这些钟被认为是人类和其他脊椎动物中与实际年龄高度相关的分子指标。此外,人们还广泛研究了它们在量化生物衰老率以及测试长寿或返老还童干预措施方面的潜力。在这里,我们讨论了理解时钟机制和生物标志物效用的关键挑战。这需要在单细胞、组织和疾病特异性模型中剖析与年龄相关变化相关的驱动因素和调节因素,以及探索其他表观遗传标记、纵向和多样化的人群研究以及非人类模型。我们还强调了法医年龄鉴定和预测个体生物衰老轨迹中的重要伦理问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f6b/6876109/db9647b8cba3/13059_2019_1824_Fig1_HTML.jpg

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