4.8 Article

Specificity of the DNA Mismatch Repair System (MMR) and Mutagenesis Bias in Bacteria

Journal

MOLECULAR BIOLOGY AND EVOLUTION
Volume 35, Issue 10, Pages 2414-2421

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/molbev/msy134

Keywords

DNA mismatch repair; mutation rate and spectrum; neutral evolution; spontaneous mutation

Funding

  1. Fundamental Research Funds for the Central Universities of China [201822020]
  2. National Natural Science Foundation of China [31741071]
  3. US Army Research Office [W911NF-09-1-0444, W911NF-14-1-0411]
  4. National Institutes of Health [R01-GM036827, R35-GM122566]
  5. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM036827, R35GM122566] Funding Source: NIH RePORTER

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The mutation rate of an organism is influenced by the interaction of evolutionary forces such as natural selection and genetic drift. However, the mutation spectrum (i.e., the frequency distribution of different types of mutations) can be heavily influenced by DNA repair. Using mutation-accumulation lines of the extremophile bacterium Deinococcus radiodurans Delta mutS1 and the model soil bacterium Pseudomonas fluorescens wild-type and MMR- (Methyl-dependent Mismatch Repair-deficient) strains, we report the mutational features of these two important bacteria. We find that P. fluorescens has one of the highest MMR repair efficiencies among tested bacteria. We also discover that MMR of D. radiodurans preferentially repairs deletions, contrary to all other bacteria examined. We then, for the first time, quantify genome-wide efficiency and specificity of MMR in repairing different genomic regions and mutation types, by evaluating the P. fluorescens and D. radiodurans mutation data sets, along with previously reported ones of Bacillus subtilis subsp. subtilis, Escherichia coli, Vibrio cholerae, and V. fischeri. MMR in all six bacteria shares two general features: 1) repair efficiency is influenced by the neighboring base composition for both transitions and transversions, not limited to transversions as previously reported; and 2) MMR only recognizes indels <4 bp in length. This study demonstrates the power of mutation accumulation lines in quantifying DNA repair and mutagenesis patterns.

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