Crosstalk between chromatin state and ATM signalling in DNA damage-induced transcription stress

The DNA Damage Response (DDR) is a highly regulated process that safeguards genomic integrity against DNA lesions. Increasing evidence supports a reciprocal relationship between damaged chromatin architecture and the signalling pathways that coordinate the DDR. However, the mechanisms underlying this interplay in response to transcription-blocking DNA lesions remain largely unexplored. Here, we show that stalling of RNA polymerase II (RNAPII) at such lesions induces local chromatin acetylation, mediated primarily by the histone acetyltransferase p300. The resulting chromatin relaxation stimulates the dissociation of mature co-transcriptional spliceosomes from nascent RNA and promotes RNA:DNA hybrid (R-loop) formation, leading to ATM activation. In turn, activated ATM modulates chromatin conformation by phosphorylating histone H2A.X and triggering p38MAPK/MSK1-dependent histone H3S10 phosphorylation. Our findings highlight the cross-regulation between chromatin state and ATM signalling as a key component of the cellular response to transcription stress.

Authors

Institutions

Publication Details

Journal
The EMBO Journal
Published
2025-08-26
DOI
https://doi.org/10.1038/s44318-025-00537-7
Primary Topic
DNA Repair Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Crosstalk between chromatin state and ATM signalling in DNA damage-induced transcription stress

Maria Tresini, Wim Vermeulen, Maarten Klunder, Irene Salas‐Armenteros
The EMBO Journal
DNA Repair Mechanisms
article

Crosstalk between chromatin state and ATM signalling in DNA damage-induced transcription stress

Maria Tresini, Wim Vermeulen, Maarten Klunder, Irene Salas‐Armenteros
article en

Abstract

The DNA Damage Response (DDR) is a highly regulated process that safeguards genomic integrity against DNA lesions. Increasing evidence supports a reciprocal relationship between damaged chromatin architecture and the signalling pathways that coordinate the DDR. However, the mechanisms underlying this interplay in response to transcription-blocking DNA lesions remain largely unexplored. Here, we show that stalling of RNA polymerase II (RNAPII) at such lesions induces local chromatin acetylation, mediated primarily by the histone acetyltransferase p300. The resulting chromatin relaxation stimulates the dissociation of mature co-transcriptional spliceosomes from nascent RNA and promotes RNA:DNA hybrid (R-loop) formation, leading to ATM activation. In turn, activated ATM modulates chromatin conformation by phosphorylating histone H2A.X and triggering p38MAPK/MSK1-dependent histone H3S10 phosphorylation. Our findings highlight the cross-regulation between chromatin state and ATM signalling as a key component of the cellular response to transcription stress.

The EMBO JournalVol. 44(19)
Erasmus MC Cancer Institute (NL)
Worldwide Cancer Research, Nederlandse Organisatie voor Wetenschappelijk Onderzoek, KWF Kankerbestrijding, European Research Council
Openalex Percentile: Top 80%
DNA Repair Mechanisms
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Crosstalk between chromatin state and ATM signalling in DNA damage-induced transcription stress — Maria Tresini, Wim Vermeulen, et al. · The EMBO Journal (2025) | TGRS Research Map | TGRS