State Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China; Key Laboratory of Genetic Network Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.
State Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China; Key Laboratory of Genetic Network Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China.
Genomics Proteomics Bioinformatics. 2018 Aug;16(4):234-243. doi: 10.1016/j.gpb.2018.07.002. Epub 2018 Sep 6.
DNA methylation is an important epigenetic mark that plays a vital role in gene expression and cell differentiation. The average DNA methylation level among a group of cells has been extensively documented. However, the cell-to-cell heterogeneity in DNA methylation, which reflects the differentiation of epigenetic status among cells, remains less investigated. Here we established a gold standard of the cell-to-cell heterogeneity in DNA methylation based on single-cell bisulfite sequencing (BS-seq) data. With that, we optimized a computational pipeline for estimating the heterogeneity in DNA methylation from bulk BS-seq data. We further built HeteroMeth, a database for searching, browsing, visualizing, and downloading the data for heterogeneity in DNA methylation for a total of 141 samples in humans, mice, Arabidopsis, and rice. Three genes are used as examples to illustrate the power of HeteroMeth in the identification of unique features in DNA methylation. The optimization of the computational strategy and the construction of the database in this study complement the recent experimental attempts on single-cell DNA methylomes and will facilitate the understanding of epigenetic mechanisms underlying cell differentiation and embryonic development. HeteroMeth is publicly available at http://qianlab.genetics.ac.cn/HeteroMeth.
DNA 甲基化是一种重要的表观遗传标记,在基因表达和细胞分化中起着至关重要的作用。一组细胞的平均 DNA 甲基化水平已经得到了广泛的研究。然而,细胞间 DNA 甲基化的异质性,反映了细胞间表观遗传状态的分化,仍然较少被研究。在这里,我们基于单细胞亚硫酸氢盐测序(BS-seq)数据,建立了细胞间 DNA 甲基化异质性的金标准。在此基础上,我们优化了一种从批量 BS-seq 数据估计 DNA 甲基化异质性的计算流程。我们进一步构建了 HeteroMeth,这是一个用于搜索、浏览、可视化和下载人类、小鼠、拟南芥和水稻共 141 个样本 DNA 甲基化异质性数据的数据库。我们以三个基因为例,说明了 HeteroMeth 在鉴定 DNA 甲基化独特特征方面的强大功能。本研究中计算策略的优化和数据库的构建,补充了最近在单细胞 DNA 甲基组学方面的实验尝试,将有助于理解细胞分化和胚胎发育背后的表观遗传机制。HeteroMeth 可在 http://qianlab.genetics.ac.cn/HeteroMeth 上公开获取。