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甲基化胞嘧啶(MC)分析:一种在全基因组亚硫酸氢盐测序数据中分析DNA甲基化异质性的新方法。

MC profiling: a novel approach to analyze DNA methylation heterogeneity in genome-wide bisulfite sequencing data.

作者信息

De Riso Giulia, Sarnataro Antonella, Scala Giovanni, Cuomo Mariella, Della Monica Rosa, Amente Stefano, Chiariotti Lorenzo, Miele Gennaro, Cocozza Sergio

机构信息

Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, via Sergio Pansini 5, 80131 Naples, Italy.

Department of Biology, University of Naples Federico II, Via Vicinale Cupa Cintia 21, 80126 Naples, Italy.

出版信息

NAR Genom Bioinform. 2022 Dec 31;4(4):lqac096. doi: 10.1093/nargab/lqac096. eCollection 2022 Dec.

DOI:10.1093/nargab/lqac096
PMID:36601577
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9803872/
Abstract

DNA methylation is an epigenetic mark implicated in crucial biological processes. Most of the knowledge about DNA methylation is based on bulk experiments, in which DNA methylation of genomic regions is reported as average methylation. However, average methylation does not inform on how methylated cytosines are distributed in each single DNA molecule. Here, we propose Methylation Class (MC) profiling as a genome-wide approach to the study of DNA methylation heterogeneity from bulk bisulfite sequencing experiments. The proposed approach is built on the concept of MCs, groups of DNA molecules sharing the same number of methylated cytosines. The relative abundances of MCs from sequencing reads incorporates the information on the average methylation, and directly informs on the methylation level of each molecule. By applying our approach to publicly available bisulfite-sequencing datasets, we individuated cell-to-cell differences as the prevalent contributor to methylation heterogeneity. Moreover, we individuated signatures of loci undergoing imprinting and X-inactivation, and highlighted differences between the two processes. When applying MC profiling to compare different conditions, we identified methylation changes occurring in regions with almost constant average methylation. Altogether, our results indicate that MC profiling can provide useful insights on the epigenetic status and its evolution at multiple genomic regions.

摘要

DNA甲基化是一种与关键生物学过程相关的表观遗传标记。目前关于DNA甲基化的大部分知识都基于大量实验,在这些实验中,基因组区域的DNA甲基化被报告为平均甲基化水平。然而,平均甲基化水平并不能说明甲基化的胞嘧啶在每个单个DNA分子中是如何分布的。在此,我们提出甲基化类别(MC)分析,作为一种从大量亚硫酸氢盐测序实验中研究DNA甲基化异质性的全基因组方法。所提出的方法基于MC的概念,即共享相同数量甲基化胞嘧啶的DNA分子组。测序读数中MC的相对丰度包含了平均甲基化的信息,并直接反映了每个分子的甲基化水平。通过将我们的方法应用于公开可用的亚硫酸氢盐测序数据集,我们确定细胞间差异是甲基化异质性的主要贡献因素。此外,我们确定了经历印记和X染色体失活的基因座特征,并突出了这两个过程之间的差异。当应用MC分析来比较不同条件时,我们识别出在平均甲基化水平几乎恒定的区域中发生的甲基化变化。总之,我们的结果表明,MC分析可以为多个基因组区域的表观遗传状态及其演变提供有用的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c448/9803872/a53fdb60e0df/lqac096fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c448/9803872/ddc917f39401/lqac096fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c448/9803872/e67a424f5a67/lqac096fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c448/9803872/9aa25af8d0f4/lqac096fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c448/9803872/4b99ce796d40/lqac096fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c448/9803872/abec27a7fab8/lqac096fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c448/9803872/1c77907ee6b1/lqac096fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c448/9803872/a53fdb60e0df/lqac096fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c448/9803872/ddc917f39401/lqac096fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c448/9803872/e67a424f5a67/lqac096fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c448/9803872/9aa25af8d0f4/lqac096fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c448/9803872/4b99ce796d40/lqac096fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c448/9803872/abec27a7fab8/lqac096fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c448/9803872/1c77907ee6b1/lqac096fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c448/9803872/a53fdb60e0df/lqac096fig7.jpg

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