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用于确定不同组织年龄的表观遗传衰老特征。

Epigenetic-aging-signature to determine age in different tissues.

作者信息

Koch Carmen M, Wagner Wolfgang

机构信息

Helmholtz-Institute for Biomedical Engineering, Aachen, Germany.

出版信息

Aging (Albany NY). 2011 Oct;3(10):1018-27. doi: 10.18632/aging.100395.

Abstract

All tissues of the organism are affected by aging. This process is associated with epigenetic modifications such as methylation changes at specific cytosine residues in the DNA (CpG sites). Here, we have identified an Epigenetic-Aging-Signature which is applicable for many tissues to predict donor age. DNA-methylation profiles of various cell types were retrieved from public data depositories - all using the HumanMethylation27 BeadChip platform which represents 27,578 CpG sites. Five datasets from dermis, epidermis, cervical smear, T-cells and monocytes were used for Pavlidis Template Matching to identify 19 CpG sites that are continuously hypermethylated upon aging (R>0.6; p-value<10-13). Four of these CpG sites (associated with the genes NPTX2, TRIM58, GRIA2 and KCNQ1DN) and an additional hypomethylated CpG site (BIRC4BP) were implemented in a model to predict donor age. This Epigenetic-Aging-Signature was tested on a validation group of eight independent datasets corresponding to several cell types from different tissues. Overall, the five CpG sites revealed age-associated DNA-methylation changes in all tissues. The average absolute difference between predicted and real chronological age was about 11 years. This method can be used to predict donor age in various cell preparations - for example in forensic analysis.

摘要

生物体的所有组织都会受到衰老的影响。这个过程与表观遗传修饰有关,比如DNA中特定胞嘧啶残基(CpG位点)的甲基化变化。在这里,我们确定了一种表观遗传衰老特征,它适用于许多组织来预测供体年龄。从公共数据存储库中检索了各种细胞类型的DNA甲基化谱——所有这些都使用了代表27,578个CpG位点的HumanMethylation27 BeadChip平台。来自真皮、表皮、宫颈涂片、T细胞和单核细胞的五个数据集用于帕夫利迪斯模板匹配,以识别19个在衰老过程中持续高甲基化的CpG位点(R>0.6;p值<10-13)。这些CpG位点中的四个(与NPTX2、TRIM58、GRIA2和KCNQ1DN基因相关)和另外一个低甲基化的CpG位点(BIRC4BP)被纳入一个模型来预测供体年龄。这个表观遗传衰老特征在一个由八个独立数据集组成的验证组上进行了测试,这些数据集对应于来自不同组织的几种细胞类型。总体而言,这五个CpG位点在所有组织中都显示出与年龄相关的DNA甲基化变化。预测年龄与实际 chronological 年龄之间的平均绝对差异约为11岁。这种方法可用于预测各种细胞制剂中的供体年龄——例如在法医分析中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98fa/3229965/d04152759a6f/aging-03-1018-g001.jpg

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