Cargando…
Quiescence unveils a novel mutational force in fission yeast
To maintain life across a fluctuating environment, cells alternate between phases of cell division and quiescence. During cell division, the spontaneous mutation rate is expressed as the probability of mutations per generation (Luria and Delbrück, 1943; Lea and Coulson, 1949), whereas during quiesce...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5734874/ https://www.ncbi.nlm.nih.gov/pubmed/29252184 http://dx.doi.org/10.7554/eLife.27469 |
_version_ | 1783287111242219520 |
---|---|
author | Gangloff, Serge Achaz, Guillaume Francesconi, Stefania Villain, Adrien Miled, Samia Denis, Claire Arcangioli, Benoit |
author_facet | Gangloff, Serge Achaz, Guillaume Francesconi, Stefania Villain, Adrien Miled, Samia Denis, Claire Arcangioli, Benoit |
author_sort | Gangloff, Serge |
collection | PubMed |
description | To maintain life across a fluctuating environment, cells alternate between phases of cell division and quiescence. During cell division, the spontaneous mutation rate is expressed as the probability of mutations per generation (Luria and Delbrück, 1943; Lea and Coulson, 1949), whereas during quiescence it will be expressed per unit of time. In this study, we report that during quiescence, the unicellular haploid fission yeast accumulates mutations as a linear function of time. The novel mutational landscape of quiescence is characterized by insertion/deletion (indels) accumulating as fast as single nucleotide variants (SNVs), and elevated amounts of deletions. When we extended the study to 3 months of quiescence, we confirmed the replication-independent mutational spectrum at the whole-genome level of a clonally aged population and uncovered phenotypic variations that subject the cells to natural selection. Thus, our results support the idea that genomes continuously evolve under two alternating phases that will impact on their size and composition. |
format | Online Article Text |
id | pubmed-5734874 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-57348742017-12-20 Quiescence unveils a novel mutational force in fission yeast Gangloff, Serge Achaz, Guillaume Francesconi, Stefania Villain, Adrien Miled, Samia Denis, Claire Arcangioli, Benoit eLife Genetics and Genomics To maintain life across a fluctuating environment, cells alternate between phases of cell division and quiescence. During cell division, the spontaneous mutation rate is expressed as the probability of mutations per generation (Luria and Delbrück, 1943; Lea and Coulson, 1949), whereas during quiescence it will be expressed per unit of time. In this study, we report that during quiescence, the unicellular haploid fission yeast accumulates mutations as a linear function of time. The novel mutational landscape of quiescence is characterized by insertion/deletion (indels) accumulating as fast as single nucleotide variants (SNVs), and elevated amounts of deletions. When we extended the study to 3 months of quiescence, we confirmed the replication-independent mutational spectrum at the whole-genome level of a clonally aged population and uncovered phenotypic variations that subject the cells to natural selection. Thus, our results support the idea that genomes continuously evolve under two alternating phases that will impact on their size and composition. eLife Sciences Publications, Ltd 2017-12-18 /pmc/articles/PMC5734874/ /pubmed/29252184 http://dx.doi.org/10.7554/eLife.27469 Text en © 2017, Gangloff et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Genetics and Genomics Gangloff, Serge Achaz, Guillaume Francesconi, Stefania Villain, Adrien Miled, Samia Denis, Claire Arcangioli, Benoit Quiescence unveils a novel mutational force in fission yeast |
title | Quiescence unveils a novel mutational force in fission yeast |
title_full | Quiescence unveils a novel mutational force in fission yeast |
title_fullStr | Quiescence unveils a novel mutational force in fission yeast |
title_full_unstemmed | Quiescence unveils a novel mutational force in fission yeast |
title_short | Quiescence unveils a novel mutational force in fission yeast |
title_sort | quiescence unveils a novel mutational force in fission yeast |
topic | Genetics and Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5734874/ https://www.ncbi.nlm.nih.gov/pubmed/29252184 http://dx.doi.org/10.7554/eLife.27469 |
work_keys_str_mv | AT gangloffserge quiescenceunveilsanovelmutationalforceinfissionyeast AT achazguillaume quiescenceunveilsanovelmutationalforceinfissionyeast AT francesconistefania quiescenceunveilsanovelmutationalforceinfissionyeast AT villainadrien quiescenceunveilsanovelmutationalforceinfissionyeast AT miledsamia quiescenceunveilsanovelmutationalforceinfissionyeast AT denisclaire quiescenceunveilsanovelmutationalforceinfissionyeast AT arcangiolibenoit quiescenceunveilsanovelmutationalforceinfissionyeast |