4.0 Article

Measuring DNA Damage Using the Alkaline Comet Assay in Cultured Cells

Journal

BIO-PROTOCOL
Volume 11, Issue 16, Pages -

Publisher

BIO-PROTOCOL
DOI: 10.21769/BioProtoc.4119

Keywords

DNA damage; DNA repair; DNA repair kinetics; Genotoxic agents; Oxidative stress; Reactive oxygen species

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Funding

  1. Swiss National Science Foundation
  2. Promedica Stiftung Chur
  3. Sassella Stiftung
  4. Kurt und Senta Herrmann Stiftung

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Maintenance of DNA integrity is crucial for cells to prevent diseases, and cells have evolved various DNA repair mechanisms to safeguard genetic integrity. The comet assay is a widely used method for measuring both DNA damage and its repair in cells, providing a valuable tool for assessing genotoxicity and repair kinetics.
Maintenance of DNA integrity is of pivotal importance for cells to circumvent detrimental processes that can ultimately lead to the development of various diseases. In the face of a plethora of endogenous and exogenous DNA-damaging agents, cells have evolved a variety of DNA repair mechanisms that are responsible for safeguarding genetic integrity. Given the relevance of DNA damage and its repair in disease, measuring the amount of both aspects is of considerable interest. The comet assay is a widely used method that allows the measurement of both DNA damage and its repair in cells. For this, cells are treated with DNA-damaging agents and embedded into a thin layer of agarose on top of a microscope slide. Subsequent lysis removes all protein and lipid components to leave so-called 'nucleoids' consisting of naked DNA remaining in the agarose. These nucleoids are then subjected to electrophoresis, whereby the negatively charged DNA migrates toward the anode depending on its degree of fragmentation and creates shapes resembling comets, which can be subsequently visualized and analyzed by fluorescence microscopy. The comet assay can be adapted to assess a wide variety of genotoxins and repair kinetics, in addition to both DNA single-strand and double-strand breaks. In this protocol, we describe in detail how to perform the alkaline comet assay to assess single-strand breaks and their repair using cultured human cell lines. We describe the workflow for assessing the amount of DNA damage generated by agents such as hydrogen peroxide (H2O2) and methyl-methanesulfonate (MMS) or present endogenously in cells, and how to assess the repair kinetics after such an insult. The procedure described herein is easy to follow and allows the cost-effective assessment of single-strand breaks and their repair kinetics in cultured cells.

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