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Updated: Jun 28, 2026

Imaging Mismatch Repair and Cellular Responses to DNA Damage in Bacillus subtilis
Published on: February 8, 2010
Defects in the error prevention oxidized guanine system potentiate stationary-phase mutagenesis in Bacillus subtilis
Luz E Vidales1, Lluvia C Cárdenas, Eduardo Robleto
1Department of Biology, University of Guanajuato, P.O. Box 187, Guanajuato, Gto. 36050 MEXICO.
Abstract:
Previous studies showed that a Bacillus subtilis strain deficient in mismatch repair (MMR; encoded by the mutSL operon) promoted the production of stationary-phase-induced mutations. However, overexpression of the mutSL operon did not completely suppress this process, suggesting that additional DNA repair mechanisms are involved in the generation of stationary-phase-associated mutants in this bacterium. In agreement with this hypothesis, the results presented in this work revealed that starved B. subtilis cells lacking a functional error prevention GO (8-oxo-G) system (composed of YtkD, MutM, and YfhQ) had a dramatic propensity to increase the number of stationary-phase-induced revertants. These results strongly suggest that the occurrence of mutations is exacerbated by reactive oxygen species in nondividing cells of B. subtilis having an inactive GO system. Interestingly, overexpression of the MMR system significantly diminished the accumulation of mutations in cells deficient in the GO repair system during stationary phase. These results suggest that the MMR system plays a general role in correcting base mispairing induced by oxidative stress during stationary phase. Thus, the absence or depression of both the MMR and GO systems contributes to the production of stationary-phase mutants in B. subtilis. In conclusion, our results support the idea that oxidative stress is a mechanism that generates genetic diversity in starved cells of B. subtilis, promoting stationary-phase-induced mutagenesis in this soil microorganism.
Insights
Inactive DNA repair systems, including mismatch repair (MMR) and 8-oxo-G (GO) repair, increase mutations in starved Bacillus subtilis. Oxidative stress drives this stationary-phase mutagenesis, generating genetic diversity.
Area of Science:
- Microbiology
- Molecular Biology
- Genetics
Background:
- Stationary-phase-induced mutations in Bacillus subtilis are linked to DNA repair deficiencies.
- Previous studies implicated mismatch repair (MMR) but suggested other mechanisms are involved.
Purpose of the Study:
- To investigate the role of the 8-oxo-G (GO) repair system in stationary-phase mutagenesis.
- To determine the interplay between MMR and GO systems in preventing mutations during starvation.
Main Methods:
- Comparative analysis of Bacillus subtilis strains with deficiencies in MMR and GO repair systems.
- Assessment of mutation rates under starvation conditions.
- Evaluation of the impact of MMR system overexpression on mutation accumulation.
Main Results:
- B. subtilis cells lacking functional GO repair (YtkD, MutM, YfhQ) showed a significant increase in stationary-phase mutations.
- Mutations were exacerbated by reactive oxygen species in starved cells with inactive GO systems.
- MMR system overexpression reduced mutation accumulation in GO-deficient cells, highlighting its role in correcting oxidative damage.
Conclusions:
- Both MMR and GO systems are crucial for preventing stationary-phase mutagenesis in B. subtilis.
- Oxidative stress contributes to genetic diversity by inducing mutations in starved cells.
- Combined deficiencies in MMR and GO systems significantly elevate mutagenesis during stationary phase.
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