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基于无细胞游离 DNA 来源核小体重排的生物钟。

Aging clock based on nucleosome reorganisation derived from cell-free DNA.

机构信息

School of Life Sciences, University of Essex, Colchester, UK.

出版信息

Aging Cell. 2024 May;23(5):e14100. doi: 10.1111/acel.14100. Epub 2024 Feb 9.

Abstract

Aging induces systematic changes in the distribution of nucleosomes, which affect gene expression programs. Here we reconstructed nucleosome maps based on cell-free DNA (cfDNA) extracted from blood plasma using four cohorts of people of different ages. We show that nucleosomes tend to be separated by larger genomic distances in older people, and age correlates with the nucleosome repeat length (NRL). Furthermore, we developed the first aging clock based on cfDNA nucleosomics. Machine learning based on cfDNA distance distributions allowed predicting person's age with the median absolute error of 3-3.5 years.

摘要

衰老会引起核小体分布的系统性变化,从而影响基因表达程序。在这里,我们基于从不同年龄段的四个人群的血浆中提取的无细胞 DNA (cfDNA),重建了核小体图谱。我们表明,随着年龄的增长,核小体往往会在基因组上相隔更大的距离,并且年龄与核小体重复长度 (NRL) 相关。此外,我们还基于 cfDNA 核小体组学开发了首个衰老时钟。基于 cfDNA 距离分布的机器学习可以预测个体的年龄,其中位数绝对误差为 3-3.5 年。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b58/11113261/90436e147669/ACEL-23-e14100-g003.jpg

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