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RESEARCH PAPER / 2026-01-17

Epigenetic consequences of DNA damage.

Tanya T Paull, Patricia L Opresko

Department of Molecular Biosciences, The University of Texas at Austin, Austin, TX 78712, USA. Electronic address: [email protected] of Molecular Biosciences, The University of Texas at Austin, Austin, TX 78712, USA. Electronic address: [email protected]. · pubmed

Abstract

Genome regulation is shaped not only by DNA sequence but also by epigenetic mechanisms that influence chromatin structure and gene expression. While epigenetics has classically focused on heritable DNA and histone modifications, growing evidence indicates that certain forms of DNA damage can also generate persistent changes in transcriptional states that are heritable in some scenarios. This review examines how diverse DNA damage-associated processes-including oxidative lesions, R-loops, telomeric damage, DNA double-strand breaks, and poly-ADP-ribosylation-intersect with the epigenome. We highlight the roles of oxidative DNA damage and repair in transcriptional regulation, the contribution of R-loops to gene expression and DNA methylation dynamics, and the impact of telomere-associated damage on chromatin organization and genome maintenance. DNA lesions, and in some cases DNA repair-associated proteins, can thus leave epigenetic "scars" that influence cellular identity, aging, and disease, expanding current views of epigenetic inheritance and genome stability.

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

DNA damage can lead to persistent epigenetic changes that influence cellular identity and aging. This paper is relevant as it explores the intersection of DNA damage and epigenetics, which may provide insights into the mechanisms underlying aging and age-related diseases.

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