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Extraordinary Genome Instability and Widespread Chromosome Rearrangements During Vegetative Growth
The haploid genome of the pathogenic fungus Zymoseptoria tritici is contained on “core” and “accessory” chromosomes. While 13 core chromosomes are found in all strains, as many as eight accessory chromosomes show presence/absence variation and rearrangements among field isolates. The factors influen...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Genetics Society of America
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6216587/ https://www.ncbi.nlm.nih.gov/pubmed/30072376 http://dx.doi.org/10.1534/genetics.118.301050 |
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author | Möller, Mareike Habig, Michael Freitag, Michael Stukenbrock, Eva H. |
author_facet | Möller, Mareike Habig, Michael Freitag, Michael Stukenbrock, Eva H. |
author_sort | Möller, Mareike |
collection | PubMed |
description | The haploid genome of the pathogenic fungus Zymoseptoria tritici is contained on “core” and “accessory” chromosomes. While 13 core chromosomes are found in all strains, as many as eight accessory chromosomes show presence/absence variation and rearrangements among field isolates. The factors influencing these presence/absence polymorphisms are so far unknown. We investigated chromosome stability using experimental evolution, karyotyping, and genome sequencing. We report extremely high and variable rates of accessory chromosome loss during mitotic propagation in vitro and in planta. Spontaneous chromosome loss was observed in 2 to >50% of cells during 4 weeks of incubation. Similar rates of chromosome loss in the closely related Zymoseptoria ardabiliae suggest that this extreme chromosome dynamic is a conserved phenomenon in the genus. Elevating the incubation temperature greatly increases instability of accessory and even core chromosomes, causing severe rearrangements involving telomere fusion and chromosome breakage. Chromosome losses do not affect the fitness of Zymoseptoria tritici in vitro, but some lead to increased virulence, suggesting an adaptive role of this extraordinary chromosome instability. |
format | Online Article Text |
id | pubmed-6216587 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Genetics Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-62165872018-11-07 Extraordinary Genome Instability and Widespread Chromosome Rearrangements During Vegetative Growth Möller, Mareike Habig, Michael Freitag, Michael Stukenbrock, Eva H. Genetics Investigations The haploid genome of the pathogenic fungus Zymoseptoria tritici is contained on “core” and “accessory” chromosomes. While 13 core chromosomes are found in all strains, as many as eight accessory chromosomes show presence/absence variation and rearrangements among field isolates. The factors influencing these presence/absence polymorphisms are so far unknown. We investigated chromosome stability using experimental evolution, karyotyping, and genome sequencing. We report extremely high and variable rates of accessory chromosome loss during mitotic propagation in vitro and in planta. Spontaneous chromosome loss was observed in 2 to >50% of cells during 4 weeks of incubation. Similar rates of chromosome loss in the closely related Zymoseptoria ardabiliae suggest that this extreme chromosome dynamic is a conserved phenomenon in the genus. Elevating the incubation temperature greatly increases instability of accessory and even core chromosomes, causing severe rearrangements involving telomere fusion and chromosome breakage. Chromosome losses do not affect the fitness of Zymoseptoria tritici in vitro, but some lead to increased virulence, suggesting an adaptive role of this extraordinary chromosome instability. Genetics Society of America 2018-10 2018-08-02 /pmc/articles/PMC6216587/ /pubmed/30072376 http://dx.doi.org/10.1534/genetics.118.301050 Text en Copyright © 2018 by the Genetics Society of America Available freely online through the author-supported open access option. |
spellingShingle | Investigations Möller, Mareike Habig, Michael Freitag, Michael Stukenbrock, Eva H. Extraordinary Genome Instability and Widespread Chromosome Rearrangements During Vegetative Growth |
title | Extraordinary Genome Instability and Widespread Chromosome Rearrangements During Vegetative Growth |
title_full | Extraordinary Genome Instability and Widespread Chromosome Rearrangements During Vegetative Growth |
title_fullStr | Extraordinary Genome Instability and Widespread Chromosome Rearrangements During Vegetative Growth |
title_full_unstemmed | Extraordinary Genome Instability and Widespread Chromosome Rearrangements During Vegetative Growth |
title_short | Extraordinary Genome Instability and Widespread Chromosome Rearrangements During Vegetative Growth |
title_sort | extraordinary genome instability and widespread chromosome rearrangements during vegetative growth |
topic | Investigations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6216587/ https://www.ncbi.nlm.nih.gov/pubmed/30072376 http://dx.doi.org/10.1534/genetics.118.301050 |
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