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The properties of spontaneous mutations in the opportunistic pathogen Pseudomonas aeruginosa
BACKGROUND: Natural genetic variation ultimately arises from the process of mutation. Knowledge of how the raw material for evolution is produced is necessary for a full understanding of several fundamental evolutionary concepts. We performed a mutation accumulation experiment with wild-type and mis...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4702332/ https://www.ncbi.nlm.nih.gov/pubmed/26732503 http://dx.doi.org/10.1186/s12864-015-2244-3 |
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author | Dettman, Jeremy R. Sztepanacz, Jacqueline L. Kassen, Rees |
author_facet | Dettman, Jeremy R. Sztepanacz, Jacqueline L. Kassen, Rees |
author_sort | Dettman, Jeremy R. |
collection | PubMed |
description | BACKGROUND: Natural genetic variation ultimately arises from the process of mutation. Knowledge of how the raw material for evolution is produced is necessary for a full understanding of several fundamental evolutionary concepts. We performed a mutation accumulation experiment with wild-type and mismatch-repair deficient, mutator lines of the pathogenic bacterium Pseudomonas aeruginosa, and used whole-genome sequencing to reveal the genome-wide rate, spectrum, distribution, leading/lagging bias, and context-dependency of spontaneous mutations. RESULTS: Wild-type base-pair mutation and indel rates were ~10(−10) and ~10(−11) per nucleotide per generation, respectively, and deficiencies in the mismatch-repair system caused rates to increase by over two orders of magnitude. A universal bias towards AT was observed in wild-type lines, but was reversed in mutator lines to a bias towards GC. Biases for which types of mutations occurred during replication of the leading versus lagging strand were detected reciprocally in both replichores. The distribution of mutations along the chromosome was non-random, with peaks near the terminus of replication and at positions intermediate to the replication origin and terminus. A similar distribution bias was observed along the chromosome in natural populations of P. aeruginosa. Site-specific mutation rates were higher when the focal nucleotide was immediately flanked by C:G pairings. CONCLUSIONS: Whole-genome sequencing of mutation accumulation lines allowed the comprehensive identification of mutations and revealed what factors of molecular and genomic architecture affect the mutational process. Our study provides a more complete view of how several mechanisms of mutation, mutation repair, and bias act simultaneously to produce the raw material for evolution. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-2244-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4702332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47023322016-01-07 The properties of spontaneous mutations in the opportunistic pathogen Pseudomonas aeruginosa Dettman, Jeremy R. Sztepanacz, Jacqueline L. Kassen, Rees BMC Genomics Research Article BACKGROUND: Natural genetic variation ultimately arises from the process of mutation. Knowledge of how the raw material for evolution is produced is necessary for a full understanding of several fundamental evolutionary concepts. We performed a mutation accumulation experiment with wild-type and mismatch-repair deficient, mutator lines of the pathogenic bacterium Pseudomonas aeruginosa, and used whole-genome sequencing to reveal the genome-wide rate, spectrum, distribution, leading/lagging bias, and context-dependency of spontaneous mutations. RESULTS: Wild-type base-pair mutation and indel rates were ~10(−10) and ~10(−11) per nucleotide per generation, respectively, and deficiencies in the mismatch-repair system caused rates to increase by over two orders of magnitude. A universal bias towards AT was observed in wild-type lines, but was reversed in mutator lines to a bias towards GC. Biases for which types of mutations occurred during replication of the leading versus lagging strand were detected reciprocally in both replichores. The distribution of mutations along the chromosome was non-random, with peaks near the terminus of replication and at positions intermediate to the replication origin and terminus. A similar distribution bias was observed along the chromosome in natural populations of P. aeruginosa. Site-specific mutation rates were higher when the focal nucleotide was immediately flanked by C:G pairings. CONCLUSIONS: Whole-genome sequencing of mutation accumulation lines allowed the comprehensive identification of mutations and revealed what factors of molecular and genomic architecture affect the mutational process. Our study provides a more complete view of how several mechanisms of mutation, mutation repair, and bias act simultaneously to produce the raw material for evolution. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-2244-3) contains supplementary material, which is available to authorized users. BioMed Central 2016-01-05 /pmc/articles/PMC4702332/ /pubmed/26732503 http://dx.doi.org/10.1186/s12864-015-2244-3 Text en © Dettman et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Dettman, Jeremy R. Sztepanacz, Jacqueline L. Kassen, Rees The properties of spontaneous mutations in the opportunistic pathogen Pseudomonas aeruginosa |
title | The properties of spontaneous mutations in the opportunistic pathogen Pseudomonas aeruginosa |
title_full | The properties of spontaneous mutations in the opportunistic pathogen Pseudomonas aeruginosa |
title_fullStr | The properties of spontaneous mutations in the opportunistic pathogen Pseudomonas aeruginosa |
title_full_unstemmed | The properties of spontaneous mutations in the opportunistic pathogen Pseudomonas aeruginosa |
title_short | The properties of spontaneous mutations in the opportunistic pathogen Pseudomonas aeruginosa |
title_sort | properties of spontaneous mutations in the opportunistic pathogen pseudomonas aeruginosa |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4702332/ https://www.ncbi.nlm.nih.gov/pubmed/26732503 http://dx.doi.org/10.1186/s12864-015-2244-3 |
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