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Single-cell multi-omic detection of DNA methylation and histone modifications reconstructs the dynamics of epigenomic maintenance

Abstract:
DNA methylation and histone modifications encode epigenetic information. Recently, major progress was made to measure either mark at a single-cell resolution; however, a method for simultaneous detection is lacking, preventing study of their interactions. Here, to bridge this gap, we developed scEpi2-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.
Publication status:
Published
Peer review status:
Peer reviewed

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Role:
Author
ORCID:
0000-0002-9430-7155
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Role:
Author
ORCID:
0000-0003-4203-9571
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Role:
Author
ORCID:
0000-0002-6967-5757


Publisher:
Nature Research
Journal:
Nature Methods More from this journal
Volume:
22
Issue:
10
Pages:
2042-2051
Publication date:
2025-09-25
Acceptance date:
2025-08-22
DOI:
EISSN:
1548-7105
ISSN:
1548-7091


Language:
English
Pubs id:
2293030
Local pid:
pubs:2293030
Source identifiers:
3357274
Deposit date:
2025-10-09
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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