Broad spectrum detection of DNA damage by Repair Assisted Damage Detection (RADD)

Nathaniel W. Holton, Yuval Ebenstein, Natalie R. Gassman*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review


Environmental exposures, reactive by-products of cellular metabolism, and spontaneous deamination events result in a spectrum of DNA adducts that if un-repaired threaten genomic integrity by inducing mutations, increasing instability, and contributing to the initiation and progression of cancer. Assessment of DNA adducts in cells and tissues is critical for genotoxic and carcinogenic evaluation of chemical exposure and may provide insight into the etiology of cancer. Numerous methods to characterize the formation of DNA adducts and their retention for risk assessment have been developed. However, there are still significant drawbacks to the implementation and wide-spread use of these methods, because they often require a substantial amount of biological sample, highly specialized expertise and equipment, and depending on technique, may be limited to the detection and quantification of only a handful of DNA adducts at a time. There is a pressing need for high throughput, easy to implement assays that can assess a broad spectrum of DNA lesions, allowing for faster evaluation of chemical exposures and assessment of the retention of adducts in biological samples. Here, we describe a new methodology, Repair Assisted Damage Detection (RADD), which utilizes a DNA damage processing repair enzyme cocktail to detect and modify sites of DNA damage for a subsequent gap filling reaction that labels the DNA damage sites. This ability to detect and label a broad spectrum of DNA lesions within cells, offers a novel and easy to use tool for assessing levels of DNA damage in cells that have been exposed to environmental agents or have natural variations in DNA repair capacity.

Original languageEnglish
Pages (from-to)42-49
Number of pages8
JournalDNA Repair
StatePublished - 1 Jun 2018


FundersFunder number
BeyondSeq consortium
University of South Alabama Mitchell Cancer Institute
National Institutes of Health
National Institute of Environmental Health SciencesR21ES028015
European Commission63489


    • Confocal microscopy
    • DNA adduct
    • DNA damage detection
    • DNA repair
    • Fluorescence


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