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Published on: December 22, 2023
The Role of the DNA Damage Response throughout the Papillomavirus Life Cycle
Caleb C McKinney1, Katherine L Hussmann2, Alison A McBride3
1Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA. caleb.mckinney@nih.gov.
Abstract:
The DNA damage response (DDR) maintains genomic integrity through an elaborate network of signaling pathways that sense DNA damage and recruit effector factors to repair damaged DNA. DDR signaling pathways are usurped and manipulated by the replication programs of many viruses. Here, we review the papillomavirus (PV) life cycle, highlighting current knowledge of how PVs recruit and engage the DDR to facilitate productive infection.
Insights
Papillomaviruses (PVs) hijack the DNA damage response (DDR) to ensure viral replication and infection. This review details how PVs manipulate DDR pathways to maintain genomic integrity and promote their life cycle.
Area of Science:
- Molecular Biology
- Virology
- Genetics
Background:
- The DNA damage response (DDR) is crucial for maintaining genomic stability by detecting and repairing DNA lesions.
- Viruses often exploit host cell machinery, including DDR pathways, to facilitate their replication.
- Papillomaviruses (PVs) are known to interact with host cell processes.
Purpose of the Study:
- To review the papillomavirus (PV) life cycle.
- To highlight how PVs recruit and engage the DNA damage response (DDR) pathways.
- To elucidate the mechanisms by which PVs manipulate DDR for productive infection.
Main Methods:
- Literature review of existing research on PVs and DDR.
- Analysis of current knowledge on PV-DDR interactions.
- Synthesis of information on the PV life cycle in relation to DDR.
Main Results:
- PVs actively recruit and utilize components of the host cell's DDR machinery.
- DDR factors are manipulated by PVs to support viral DNA replication and genome maintenance.
- The interaction between PVs and DDR is essential for the completion of the PV life cycle.
Conclusions:
- Papillomaviruses have evolved sophisticated strategies to co-opt the DNA damage response.
- Understanding PV-DDR interactions is key to comprehending viral pathogenesis and developing antiviral therapies.
- Targeting the DDR manipulation by PVs could offer novel therapeutic avenues.
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