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Mutation Rate, Spectrum, Topology, and Context-Dependency in the DNA Mismatch Repair-Deficient Pseudomonas fluorescens ATCC948
High levels of genetic diversity exist among natural isolates of the bacterium Pseudomonas fluorescens, and are especially elevated around the replication terminus of the genome, where strain-specific genes are found. In an effort to understand the role of genetic variation in the evolution of Pseud...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4316635/ https://www.ncbi.nlm.nih.gov/pubmed/25539726 http://dx.doi.org/10.1093/gbe/evu284 |
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author | Long, Hongan Sung, Way Miller, Samuel F. Ackerman, Matthew S. Doak, Thomas G. Lynch, Michael |
author_facet | Long, Hongan Sung, Way Miller, Samuel F. Ackerman, Matthew S. Doak, Thomas G. Lynch, Michael |
author_sort | Long, Hongan |
collection | PubMed |
description | High levels of genetic diversity exist among natural isolates of the bacterium Pseudomonas fluorescens, and are especially elevated around the replication terminus of the genome, where strain-specific genes are found. In an effort to understand the role of genetic variation in the evolution of Pseudomonas, we analyzed 31,106 base substitutions from 45 mutation accumulation lines of P. fluorescens ATCC948, naturally deficient for mismatch repair, yielding a base-substitution mutation rate of 2.34 × 10(−8) per site per generation (SE: 0.01 × 10(−8)) and a small-insertion-deletion mutation rate of 1.65 × 10(−9) per site per generation (SE: 0.03 × 10(−9)). We find that the spectrum of mutations in prophage regions, which often contain virulence factors and antibiotic resistance, is highly similar to that in the intergenic regions of the host genome. Our results show that the mutation rate varies around the chromosome, with the lowest mutation rate found near the origin of replication. Consistent with observations from other studies, we find that site-specific mutation rates are heavily influenced by the immediately flanking nucleotides, indicating that mutations are context dependent. |
format | Online Article Text |
id | pubmed-4316635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-43166352015-02-19 Mutation Rate, Spectrum, Topology, and Context-Dependency in the DNA Mismatch Repair-Deficient Pseudomonas fluorescens ATCC948 Long, Hongan Sung, Way Miller, Samuel F. Ackerman, Matthew S. Doak, Thomas G. Lynch, Michael Genome Biol Evol Research Article High levels of genetic diversity exist among natural isolates of the bacterium Pseudomonas fluorescens, and are especially elevated around the replication terminus of the genome, where strain-specific genes are found. In an effort to understand the role of genetic variation in the evolution of Pseudomonas, we analyzed 31,106 base substitutions from 45 mutation accumulation lines of P. fluorescens ATCC948, naturally deficient for mismatch repair, yielding a base-substitution mutation rate of 2.34 × 10(−8) per site per generation (SE: 0.01 × 10(−8)) and a small-insertion-deletion mutation rate of 1.65 × 10(−9) per site per generation (SE: 0.03 × 10(−9)). We find that the spectrum of mutations in prophage regions, which often contain virulence factors and antibiotic resistance, is highly similar to that in the intergenic regions of the host genome. Our results show that the mutation rate varies around the chromosome, with the lowest mutation rate found near the origin of replication. Consistent with observations from other studies, we find that site-specific mutation rates are heavily influenced by the immediately flanking nucleotides, indicating that mutations are context dependent. Oxford University Press 2014-12-23 /pmc/articles/PMC4316635/ /pubmed/25539726 http://dx.doi.org/10.1093/gbe/evu284 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Long, Hongan Sung, Way Miller, Samuel F. Ackerman, Matthew S. Doak, Thomas G. Lynch, Michael Mutation Rate, Spectrum, Topology, and Context-Dependency in the DNA Mismatch Repair-Deficient Pseudomonas fluorescens ATCC948 |
title | Mutation Rate, Spectrum, Topology, and Context-Dependency in the DNA Mismatch Repair-Deficient Pseudomonas fluorescens ATCC948 |
title_full | Mutation Rate, Spectrum, Topology, and Context-Dependency in the DNA Mismatch Repair-Deficient Pseudomonas fluorescens ATCC948 |
title_fullStr | Mutation Rate, Spectrum, Topology, and Context-Dependency in the DNA Mismatch Repair-Deficient Pseudomonas fluorescens ATCC948 |
title_full_unstemmed | Mutation Rate, Spectrum, Topology, and Context-Dependency in the DNA Mismatch Repair-Deficient Pseudomonas fluorescens ATCC948 |
title_short | Mutation Rate, Spectrum, Topology, and Context-Dependency in the DNA Mismatch Repair-Deficient Pseudomonas fluorescens ATCC948 |
title_sort | mutation rate, spectrum, topology, and context-dependency in the dna mismatch repair-deficient pseudomonas fluorescens atcc948 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4316635/ https://www.ncbi.nlm.nih.gov/pubmed/25539726 http://dx.doi.org/10.1093/gbe/evu284 |
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