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Updated: Apr 8, 2026

A Simple, Rapid, and Quantitative Assay to Measure Repair of DNA-protein Crosslinks on Plasmids Transfected into Mammalian Cells
Published on: March 5, 2018
DNA-protein crosslink repair
Julian Stingele1, Stefan Jentsch2
1Department of Molecular Cell Biology, Max Planck Institute of Biochemistry, Am Klopferspitz 18, 82152 Martinsried, Germany. Present address: The Francis Crick Institute, Clare Hall Laboratory, Blanche Lane, South Mimms, Hertfordshire EN6 3LD, UK.
Abstract:
DNA-protein crosslinks (DPCs) are highly toxic DNA adducts, but whether dedicated DPC-repair mechanisms exist was until recently unknown. This has changed with discoveries made in yeast and Xenopus laevis that revealed a protease-based DNA-repair pathway specific for DPCs. Importantly, mutations in the gene encoding the putative human homologue of a yeast DPC protease cause a human premature ageing and cancer predisposition syndrome. Thus, DPC repair is a previously overlooked genome-maintenance mechanism that may be essential for tumour suppression.
Insights
Scientists discovered a new DNA repair pathway that removes toxic DNA-protein crosslinks (DPCs). This pathway is crucial for preventing premature aging and cancer, highlighting its role in genome maintenance and tumor suppression.
Area of Science:
- Molecular Biology
- Genetics
- Biochemistry
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