Division of Computational Genomics and Systems Genetics, German Cancer Research Center, Heidelberg, Germany.
Genome Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany.
Nat Commun. 2024 Aug 31;15(1):7567. doi: 10.1038/s41467-024-51833-5.
Ageing is the accumulation of changes and decline of function of organisms over time. The concept and biomarkers of biological age have been established, notably DNA methylation-based clocks. The emergence of single-cell DNA methylation profiling methods opens the possibility of studying the biological age of individual cells. Here, we generate a large single-cell DNA methylation and transcriptome dataset from mouse peripheral blood samples, spanning a broad range of ages. The number of genes expressed increases with age, but gene-specific changes are small. We next develop scEpiAge, a single-cell DNA methylation age predictor, which can accurately predict age in (very sparse) publicly available datasets, and also in single cells. DNA methylation age distribution is wider than technically expected, indicating epigenetic age heterogeneity and functional differences. Our work provides a foundation for single-cell and sparse data epigenetic age predictors, validates their functionality and highlights epigenetic heterogeneity during ageing.
衰老是生物体随时间推移而发生的变化和功能衰退的积累。生物年龄的概念和生物标志物已经建立,特别是基于 DNA 甲基化的时钟。单细胞 DNA 甲基化分析方法的出现为研究单个细胞的生物年龄提供了可能。在这里,我们从小鼠外周血样本中生成了一个大型的单细胞 DNA 甲基化和转录组数据集,涵盖了广泛的年龄范围。随着年龄的增长,表达的基因数量增加,但基因特异性变化很小。接下来,我们开发了 scEpiAge,一种单细胞 DNA 甲基化年龄预测器,它可以准确预测(非常稀疏)公开可用数据集以及单细胞中的年龄。DNA 甲基化年龄分布比技术上预期的要宽,这表明表观遗传年龄异质性和功能差异。我们的工作为单细胞和稀疏数据表观遗传年龄预测器提供了基础,验证了它们的功能,并强调了衰老过程中的表观遗传异质性。