Related Experiment Video
Updated: Jun 7, 2026

Using Next Generation Sequencing to Identify Mutations Associated with Repair of a CAS9-induced Double Strand Break Near the CD4 Promoter
Published on: March 31, 2022
Direct inhibition of excision/synthesis DNA repair activities by cadmium: analysis on dedicated biochips
1CEA, INAC, SCIB, UJF & CNRS, LCIB (UMR_E 3 CEA-UJF and FRE 3200), Laboratoire Lésions des Acides Nucléiques, 17 Rue des Martyrs, F-38054 Grenoble Cedex 9, France. serge.candeias@cea.fr
Abstract:
The well established toxicity of cadmium and cadmium compounds results from their additive effects on several key cellular processes, including DNA repair. Mammalian cells have evolved several biochemical pathways to repair DNA lesions and maintain genomic integrity. By interfering with the homeostasis of redox metals and antioxidant systems, cadmium promotes the development of an intracellular environment that results in oxidative DNA damage which can be mutagenic if unrepaired. Small base lesions are recognised by specialized glycosylases and excised from the DNA molecule. The resulting abasic sites are incised, and the correct sequences restored by DNA polymerases using the opposite strands as template. Bulky lesions are recognised by a different set of proteins and excised from DNA as part of an oligonucleotide. As in base repair, the resulting gaps are filled by DNA polymerases using the opposite strands as template. Thus, these two repair pathways consist in excision of the lesion followed by DNA synthesis. In this study, we analysed in vitro the direct effects of cadmium exposure on the functionality of base and nucleotide DNA repair pathways. To this end, we used recently described dedicated microarrays that allow the parallel monitoring in cell extracts of the repair activities directed against several model base and/or nucleotide lesions. Both base and nucleotide excision/repair pathways are inhibited by CdCl₂, with different sensitivities. The inhibitory effects of cadmium affect mainly the recognition and excision stages of these processes. Furthermore, our data indicate that the repair activities directed against different damaged bases also exhibit distinct sensitivities, and the direct comparison of cadmium effects on the excision of uracile in different sequences even allows us to propose a hierarchy of cadmium sensibility within the glycosylases removing U from DNA. These results indicate that, in our experimental conditions, cadmium is a very potent DNA repair poison.
Insights
Cadmium (CdCl₂) is a potent DNA repair poison, inhibiting both base and nucleotide excision repair pathways by affecting lesion recognition and removal. This interference with DNA repair mechanisms can lead to mutagenic damage.
Area of Science:
- Environmental toxicology
- Molecular biology
- Genetics
Background:
- Cadmium toxicity stems from disrupting cellular processes, including DNA repair.
- Oxidative stress induced by cadmium can cause mutagenic DNA damage.
- Mammalian cells possess intricate DNA repair pathways to maintain genomic integrity.
Purpose of the Study:
- To investigate the direct in vitro effects of cadmium exposure on DNA repair pathway functionality.
- To analyze cadmium's impact on base excision repair (BER) and nucleotide excision repair (NER) pathways.
- To determine the sensitivity of different DNA repair mechanisms and specific enzymes to cadmium.
Main Methods:
- Utilized dedicated microarrays for parallel monitoring of DNA repair activities against model lesions in cell extracts.
- Assessed the inhibitory effects of CdCl₂ on both BER and NER pathways.
- Compared the sensitivity of different damaged base repair activities and glycosylases to cadmium.
Main Results:
- Cadmium chloride (CdCl₂) significantly inhibits both base and nucleotide excision/repair pathways, with varying sensitivities.
- Cadmium's inhibitory effects primarily target the recognition and excision stages of DNA repair.
- Distinct sensitivities were observed for repair activities against different damaged bases, establishing a hierarchy of cadmium sensibility for uracil-excising glycosylases.
Conclusions:
- Cadmium acts as a potent inhibitor of DNA repair mechanisms in vitro.
- The interference with DNA repair highlights a critical aspect of cadmium toxicity.
- Understanding cadmium's impact on DNA repair is crucial for assessing its genotoxic and mutagenic potential.
More Related Videos
Related Concept Videos
DNA Damage can Stall the Cell Cycle
DNA Damage Can Stall the Cell Cycle
Base Excision Repair
The first step of...

