表观遗传学
DNA甲基化
组蛋白
染色质
计算生物学
表观遗传学
DNA
RNA导向的DNA甲基化
生物
组蛋白甲基化
癌症表观遗传学
甲基化
体育锻炼的表观遗传学
CpG站点
照明菌甲基化试验
组蛋白密码
细胞生物学
甲基化DNA免疫沉淀
遗传学
分子生物学
组蛋白H2A
组蛋白甲基转移酶
染色质重塑
差异甲基化区
组蛋白H3
作者
Christoph Geisenberger,Jeroen van den Berg,Vincent van Batenburg,Buys de Barbanson,Anna Lyubimova,Joe Verity-Legg,Xiufei Chen,Yibin Liu,Chun‐Xiao Song,Jeroen de Ridder,Alexander van Oudenaarden
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2025-09-25
卷期号:22 (10): 2042-2051
被引量:7
标识
DOI:10.1038/s41592-025-02847-4
摘要
-seq. Our technique provides a readout of histone modifications and DNA methylation at the single-cell and single-molecule level. Application in a cell line with the FUCCI cell cycle reporter system reveals how DNA methylation maintenance is influenced by the local chromatin context. In addition, profiling of H3K27me3 and DNA methylation in the mouse intestine yields insights into epigenetic interactions during cell type specification. Differentially methylated regions also demonstrated independent cell-type regulation in addition to H3K27me3 regulation, which reinforces that CpG methylation acts as an additional layer of control in facultative heterochromatin.
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