This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Pedraza-Reyes, M.
Right arrow Articles by Yasbin, R. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Pedraza-Reyes, M.
Right arrow Articles by Yasbin, R. E.

 Previous Article  |  Next Article 

Journal of Bacteriology, October 2004, p. 6485-6491, Vol. 186, No. 19
0021-9193/04/$08.00+0     DOI: 10.1128/JB.186.19.6485-6491.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Contribution of the Mismatch DNA Repair System to the Generation of Stationary-Phase-Induced Mutants of Bacillus subtilis

Mario Pedraza-Reyes1 and Ronald E. Yasbin2*

Institute of Investigation in Experimental Biology, Faculty of Chemistry, University of Guanajuato, Guanajuato, Guanajuato, Mexico,1 Department of Molecular and Cell Biology, The University of Texas at Dallas, Richardson, Texas2

Received 24 March 2004/ Accepted 1 July 2004

A reversion assay system previously implemented to demonstrate the existence of adaptive or stationary-phase-induced mutagenesis in Bacillus subtilis was utilized in this report to study the influence of the mismatch DNA repair (MMR) system on this type of mutagenesis. Results revealed that a strain deficient in MutSL showed a significant propensity to generate increased numbers of stationary-phase-induced revertants. These results suggest that absence or depression of MMR is an important factor in the mutagenesis of nongrowing B. subtilis cells because of the role of MMR in repairing DNA damage. In agreement with this suggestion, a significant decrease in the number of adaptive revertant colonies, for the three markers tested, occurred in B. subtilis cells which overexpressed a component of the MMR system. Interestingly, the single overexpression of mutS, but not of mutL, was sufficient to decrease the level of adaptive mutants in the reversion assay system of B. subtilis. The results presented in this work, as well as in our previous studies, appear to suggest that an MMR deficiency, putatively attributable to inactivation or saturation with DNA damage of MutS, may occur in a subset of B. subtilis cells that differentiate into the hypermutable state.


* Corresponding author. Mailing address: College of Sciences, University of Nevada—Las Vegas, 4505 Maryland Parkway, Box 454001, Las Vegas, NV 89154-4001. Phone: (702) 895-3487. Fax: (702) 895-4159. E-mail: Ronald.yasbin{at}ccmail.nevada.edu.


Journal of Bacteriology, October 2004, p. 6485-6491, Vol. 186, No. 19
0021-9193/04/$08.00+0     DOI: 10.1128/JB.186.19.6485-6491.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Vidales, L. E., Cardenas, L. C., Robleto, E., Yasbin, R. E., Pedraza-Reyes, M. (2009). Defects in the Error Prevention Oxidized Guanine System Potentiate Stationary-Phase Mutagenesis in Bacillus subtilis. J. Bacteriol. 191: 506-513 [Abstract] [Full Text]  
  • Cirz, R. T., Jones, M. B., Gingles, N. A., Minogue, T. D., Jarrahi, B., Peterson, S. N., Romesberg, F. E. (2007). Complete and SOS-Mediated Response of Staphylococcus aureus to the Antibiotic Ciprofloxacin. J. Bacteriol. 189: 531-539 [Abstract] [Full Text]  
  • Ross, C., Pybus, C., Pedraza-Reyes, M., Sung, H.-M., Yasbin, R. E., Robleto, E. (2006). Novel Role of mfd: Effects on Stationary-Phase Mutagenesis in Bacillus subtilis. J. Bacteriol. 188: 7512-7520 [Abstract] [Full Text]  
  • Cirz, R. T., Romesberg, F. E. (2006). Induction and Inhibition of Ciprofloxacin Resistance-Conferring Mutations in Hypermutator Bacteria. Antimicrob. Agents Chemother. 50: 220-225 [Abstract] [Full Text]