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De Novo Mutation Rate Variation and Its Determinants in Chlamydomonas
De novo mutations are central for evolution, since they provide the raw material for natural selection by regenerating genetic variation. However, studying de novo mutations is challenging and is generally restricted to model species, so we have a limited understanding of the evolution of the mutati...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383909/ https://www.ncbi.nlm.nih.gov/pubmed/33950243 http://dx.doi.org/10.1093/molbev/msab140 |
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author | López-Cortegano, Eugenio Craig, Rory J Chebib, Jobran Samuels, Toby Morgan, Andrew D Kraemer, Susanne A Böndel, Katharina B Ness, Rob W Colegrave, Nick Keightley, Peter D |
author_facet | López-Cortegano, Eugenio Craig, Rory J Chebib, Jobran Samuels, Toby Morgan, Andrew D Kraemer, Susanne A Böndel, Katharina B Ness, Rob W Colegrave, Nick Keightley, Peter D |
author_sort | López-Cortegano, Eugenio |
collection | PubMed |
description | De novo mutations are central for evolution, since they provide the raw material for natural selection by regenerating genetic variation. However, studying de novo mutations is challenging and is generally restricted to model species, so we have a limited understanding of the evolution of the mutation rate and spectrum between closely related species. Here, we present a mutation accumulation (MA) experiment to study de novo mutation in the unicellular green alga Chlamydomonas incerta and perform comparative analyses with its closest known relative, Chlamydomonas reinhardtii. Using whole-genome sequencing data, we estimate that the median single nucleotide mutation (SNM) rate in C. incerta is μ = 7.6 × 10(−10), and is highly variable between MA lines, ranging from μ = 0.35 × 10(−10) to μ = 131.7 × 10(−10). The SNM rate is strongly positively correlated with the mutation rate for insertions and deletions between lines (r > 0.97). We infer that the genomic factors associated with variation in the mutation rate are similar to those in C. reinhardtii, allowing for cross-prediction between species. Among these genomic factors, sequence context and complexity are more important than GC content. With the exception of a remarkably high C→T bias, the SNM spectrum differs markedly between the two Chlamydomonas species. Our results suggest that similar genomic and biological characteristics may result in a similar mutation rate in the two species, whereas the SNM spectrum has more freedom to diverge. |
format | Online Article Text |
id | pubmed-8383909 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-83839092021-08-25 De Novo Mutation Rate Variation and Its Determinants in Chlamydomonas López-Cortegano, Eugenio Craig, Rory J Chebib, Jobran Samuels, Toby Morgan, Andrew D Kraemer, Susanne A Böndel, Katharina B Ness, Rob W Colegrave, Nick Keightley, Peter D Mol Biol Evol Discoveries De novo mutations are central for evolution, since they provide the raw material for natural selection by regenerating genetic variation. However, studying de novo mutations is challenging and is generally restricted to model species, so we have a limited understanding of the evolution of the mutation rate and spectrum between closely related species. Here, we present a mutation accumulation (MA) experiment to study de novo mutation in the unicellular green alga Chlamydomonas incerta and perform comparative analyses with its closest known relative, Chlamydomonas reinhardtii. Using whole-genome sequencing data, we estimate that the median single nucleotide mutation (SNM) rate in C. incerta is μ = 7.6 × 10(−10), and is highly variable between MA lines, ranging from μ = 0.35 × 10(−10) to μ = 131.7 × 10(−10). The SNM rate is strongly positively correlated with the mutation rate for insertions and deletions between lines (r > 0.97). We infer that the genomic factors associated with variation in the mutation rate are similar to those in C. reinhardtii, allowing for cross-prediction between species. Among these genomic factors, sequence context and complexity are more important than GC content. With the exception of a remarkably high C→T bias, the SNM spectrum differs markedly between the two Chlamydomonas species. Our results suggest that similar genomic and biological characteristics may result in a similar mutation rate in the two species, whereas the SNM spectrum has more freedom to diverge. Oxford University Press 2021-05-05 /pmc/articles/PMC8383909/ /pubmed/33950243 http://dx.doi.org/10.1093/molbev/msab140 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. https://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/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Discoveries López-Cortegano, Eugenio Craig, Rory J Chebib, Jobran Samuels, Toby Morgan, Andrew D Kraemer, Susanne A Böndel, Katharina B Ness, Rob W Colegrave, Nick Keightley, Peter D De Novo Mutation Rate Variation and Its Determinants in Chlamydomonas |
title | De Novo Mutation Rate Variation and Its Determinants in Chlamydomonas |
title_full | De Novo Mutation Rate Variation and Its Determinants in Chlamydomonas |
title_fullStr | De Novo Mutation Rate Variation and Its Determinants in Chlamydomonas |
title_full_unstemmed | De Novo Mutation Rate Variation and Its Determinants in Chlamydomonas |
title_short | De Novo Mutation Rate Variation and Its Determinants in Chlamydomonas |
title_sort | de novo mutation rate variation and its determinants in chlamydomonas |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383909/ https://www.ncbi.nlm.nih.gov/pubmed/33950243 http://dx.doi.org/10.1093/molbev/msab140 |
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