Sequencing DNA methylation and hydroxymethylation at co-occurring chromatin features

Epigenetic modifications govern chromatin dynamics and cell state. However, current methods cannot simultaneously resolve the presence of multiple DNA modifications at co-occurring chromatin-associated features. It is thus not clear how these features are physically coupled and how their combinations regulate genome function. To address this key question, we report 6-base-CUT&Tag, a method for simultaneous 6-base DNA sequencing at target chromatin features. Using 6-base-CUT&Tag to profile 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC) at co-occurring histone modifications in mouse embryonic stem cells (mESCs), we identify feature-dependent 5mC/5hmC signatures previously unresolvable with untargeted or bisulfite-based workflows. We show that DNA methylation and hydroxymethylation are specifically coupled with the H3K4me1 mark in mESC enhancers and that H3K4me1-derived signatures robustly distinguish different enhancer functional states.

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Publication Details

Journal
Nature Communications
Published
2026-02-10
DOI
https://doi.org/10.1038/s41467-026-69429-6
Primary Topic
Epigenetics and DNA Methylation
Type
article
Field-Weighted Citation Impact
0.00

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article

Sequencing DNA methylation and hydroxymethylation at co-occurring chromatin features

David Tannahill, Rafael de Cesaris Araujo Tavares, Minna Taipale, Paula Golder et al.
Nature Communications
Epigenetics and DNA Methylation
article

Sequencing DNA methylation and hydroxymethylation at co-occurring chromatin features

David Tannahill, Rafael de Cesaris Araujo Tavares, Minna Taipale, Paula Golder, AC Uitz, Somdutta Dhir, Shankar Balasubramanian, Xuan He, Jack Monahan, Walraj Gosal
article en

Abstract

Epigenetic modifications govern chromatin dynamics and cell state. However, current methods cannot simultaneously resolve the presence of multiple DNA modifications at co-occurring chromatin-associated features. It is thus not clear how these features are physically coupled and how their combinations regulate genome function. To address this key question, we report 6-base-CUT&Tag, a method for simultaneous 6-base DNA sequencing at target chromatin features. Using 6-base-CUT&Tag to profile 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC) at co-occurring histone modifications in mouse embryonic stem cells (mESCs), we identify feature-dependent 5mC/5hmC signatures previously unresolvable with untargeted or bisulfite-based workflows. We show that DNA methylation and hydroxymethylation are specifically coupled with the H3K4me1 mark in mESC enhancers and that H3K4me1-derived signatures robustly distinguish different enhancer functional states.

Nature CommunicationsVol. 17(1)
University of Cambridge (GB), Cancer Research UK (GB), Cancer Research UK Cambridge Center (GB), Cambridge School (PT), Trinity House (GB)
Wellcome Trust, Cancer Research UK, Cancer Research UK Cambridge Institute, University of Cambridge
Openalex Percentile: Top 62%
Epigenetics and DNA Methylation
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