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Updated: Jun 22, 2026

Visualizing and Quantifying Endonuclease-Based Site-Specific DNA Damage
Published on: August 21, 2021
Viral manipulation of DNA repair and cell cycle checkpoints
Mira S Chaurushiya1, Matthew D Weitzman
1Laboratory of Genetics, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Abstract:
Recognition and repair of DNA damage is critical for maintaining genomic integrity and suppressing tumorigenesis. In eukaryotic cells, the sensing and repair of DNA damage are coordinated with cell cycle progression and checkpoints, in order to prevent the propagation of damaged DNA. The carefully maintained cellular response to DNA damage is challenged by viruses, which produce a large amount of exogenous DNA during infection. Viruses also express proteins that perturb cellular DNA repair and cell cycle pathways, promoting tumorigenesis in their quest for cellular domination. This review presents an overview of strategies employed by viruses to manipulate DNA damage responses and cell cycle checkpoints as they commandeer the cell to maximize their own viral replication. Studies of viruses have identified key cellular regulators and revealed insights into molecular mechanisms governing DNA repair, cell cycle checkpoints, and transformation.
Insights
Viruses disrupt cellular DNA repair and cell cycle checkpoints to promote their replication and tumorigenesis. Studying viral manipulation reveals key regulators of DNA repair and cell cycle control.
Area of Science:
- Molecular Biology
- Virology
- Cell Biology
Background:
- DNA damage recognition and repair are vital for genomic stability and preventing cancer.
- Cellular DNA repair and cell cycle checkpoints are tightly regulated to prevent damaged DNA propagation.
- Viruses challenge these cellular mechanisms by introducing foreign DNA and expressing viral proteins.
Purpose of the Study:
- To review viral strategies for manipulating host DNA damage responses and cell cycle checkpoints.
- To highlight how viruses exploit cellular machinery for their own replication.
- To underscore the insights gained from viral studies into fundamental cellular processes.
Main Methods:
- Literature review of viral interactions with host DNA repair pathways.
- Analysis of viral protein functions in modulating cell cycle progression.
- Synthesis of current knowledge on virus-induced genomic instability and transformation.
Main Results:
- Viruses employ diverse strategies to evade or subvert host DNA damage surveillance and repair.
- Viral proteins can directly interfere with DNA repair enzymes and cell cycle regulators.
- Viral manipulation of these pathways often contributes to viral replication and oncogenesis.
Conclusions:
- Understanding viral hijacking of DNA damage responses provides critical insights into cancer development.
- Viral studies have identified key cellular proteins involved in DNA repair and cell cycle control.
- Targeting viral manipulation of these pathways could offer new therapeutic strategies for viral infections and cancer.
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