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.

Journal of Bacteriology
|November 18, 2008
PubMed

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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