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Carcinogens can induce homologous recombination between duplicated chromosomal sequences in mouse L cells
Y Y Wang1, V M Maher, R M Liskay
1Department of Microbiology, Michigan State University, East Lansing 48824-1316.
Abstract:
The ability of a series of DNA-damaging agents to induce homologous intrachromosomal recombination between duplicated genes in the chromosome of mouse cells was investigated. The target cells were the thymidine kinase-deficient mouse L-cell strain 333M, which contains a single integrated copy of a plasmid with two herpes simplex virus thymidine kinase (Htk) genes, each containing an 8-base-pair XhoI linker inserted at a unique site. Expression of a functional Htk enzyme requires a productive recombinational event between the two nonfunctional genes. The spontaneous rate of recombination in this strain is 3 per 10(6) cells per generation. The agents tested represent physical carcinogens (UV and ionizing radiation), a simple alkylating agent (N-methyl-N'-nitro-N-nitrosoguanidine), an alkylating cross-linking agent (mitomycin C), and a reactive metabolite of a polycyclic aromatic hydrocarbon ((+/-)-7 beta,8 alpha-dihydroxy-9 alpha,10 alpha-epoxy-7,8,9,10- tetrahydrobenzo[a]pyrene [BPDE] ). The background frequency of tk+ recombinants in the untreated population averaged 18 X 10(-6) +/- 5 X 10(-6). Ionizing radiation had little or no effect on recombination; exposure to mitomycin C, N-methyl-N'-nitro-N-nitrosoguanidine, BPDE, or UV, at doses that lowered the survival to between 90 and 10% of the control, caused a dose-dependent increase in frequency of recombinants, reaching 50 X 10(-6) to 100 X 10(-6). No tk+ cells could be generated with a control cell line that contained only one mutant copy of the Htk gene. Molecular hybridization analysis showed that 85 to 90% of the tk+ recombinants retained the Htk gene duplication, consistent with nonreciprocal transfer of wild-type genetic information, gene conversion. In the rest, only a single copy of the Htk gene remained, reflecting a single reciprocal exchange within a chromatid or a single unequal exchange between sister chromatids. Each recombinant tested contained an XhoI-resistant (wild-type) Htk gene.
Insights
DNA-damaging agents like UV and BPDE significantly increase homologous recombination in mouse cells. This study investigated how various carcinogens induce genetic recombination, revealing dose-dependent increases in thymidine kinase (tk+) recombinants.
Area of Science:
- Molecular Biology
- Genetics
- Carcinogenesis
Background:
- Homologous intrachromosomal recombination is a key DNA repair mechanism.
- Understanding recombination induction by DNA-damaging agents is crucial for cancer research.
- Mouse L-cell strain 333M provides a model system with duplicated herpes simplex virus thymidine kinase (Htk) genes for studying recombination.
Purpose of the Study:
- To investigate the ability of various DNA-damaging agents to induce homologous intrachromosomal recombination.
- To quantify the dose-dependent effect of physical and chemical carcinogens on recombination frequency.
- To characterize the molecular nature of recombination events in response to DNA damage.
Main Methods:
- Utilized a mouse L-cell strain (333M) containing a single integrated plasmid with two nonfunctional Htk genes.
- Exposed cells to DNA-damaging agents: UV radiation, ionizing radiation, N-methyl-N'-nitro-N-nitrosoguanidine, mitomycin C, and BPDE.
- Assessed functional Htk enzyme expression to quantify recombination rates and employed molecular hybridization for analysis.
Main Results:
- Ionizing radiation showed minimal effect on recombination frequency.
- UV, mitomycin C, N-methyl-N'-nitro-N-nitrosoguanidine, and BPDE induced a dose-dependent increase in tk+ recombinants.
- Molecular analysis revealed gene conversion (85-90%) and reciprocal exchange (10-15%) as primary recombination mechanisms.
Conclusions:
- Certain DNA-damaging agents, including UV and BPDE, are potent inducers of homologous recombination in mammalian cells.
- The study highlights the role of gene conversion in repairing DNA damage-induced recombination events.
- Findings contribute to understanding the genotoxic mechanisms underlying chemical and physical carcinogenesis.