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Updated: Mar 20, 2026

Visualizing and Quantifying Endonuclease-Based Site-Specific DNA Damage
Published on: August 21, 2021
Epigenome Maintenance in Response to DNA Damage.
Juliette Dabin1, Anna Fortuny1, Sophie E Polo1
1Epigenome Integrity Group, UMR 7216 CNRS, Paris Diderot University, Sorbonne Paris Cité, 75013 Paris Cedex 13, France.
Maintaining cellular identity requires stable chromatin, but DNA damage disrupts this epigenome. This review explores mechanisms that restore chromatin structure and function after DNA damage in mammalian cells.
Area of Science:
- Cellular Biology
- Epigenetics
- Genomics
Background:
- Organism viability depends on stable chromatin landscapes that dictate cell functions and identities.
- Epigenome maintenance is challenged by transcription, replication, and DNA damage, causing dynamic chromatin changes.
Purpose of the Study:
- To review recent advances in understanding epigenome restoration after DNA damage.
- To explore emerging concepts and highlight open issues in epigenome maintenance during DNA repair.
- To discuss the role of nuclear organization and epigenome plasticity in genome stability.
Main Methods:
- Literature review of recent advances in epigenetics and DNA repair.
- Comparative analysis of epigenome maintenance during replication and DNA damage.
- Discussion of molecular players involved in genome and epigenome integrity.
Main Results:
- Specialized mechanisms restore epigenome structure and function post-DNA damage.
- Nuclear organization plays a crucial role in maintaining genome stability.
- Epigenome plasticity is a key factor in response to genotoxic stress.
Conclusions:
- Coordinated maintenance of genome and epigenome integrity is essential for cell survival.
- Understanding epigenome restoration mechanisms after DNA damage is critical for cellular health.
- Further research is needed to fully elucidate the functional implications of epigenome plasticity.
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