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Telomere-to-Telomere Genome Sequences across a Single Genus Reveal Highly Variable Chromosome Rearrangement Rates but Absolute Stasis of Chromosome Number
Genome rearrangements in filamentous fungi are prevalent but little is known about the modalities of their evolution, in part because few complete genomes are available within a single genus. To address this, we have generated and compared 15 complete telomere-to-telomere genomes across the phylogen...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9318876/ https://www.ncbi.nlm.nih.gov/pubmed/35887427 http://dx.doi.org/10.3390/jof8070670 |
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author | Quenu, Mathieu Treindl, Artemis D. Lee, Kate Takemoto, Daigo Thünen, Torsten Ashrafi, Samad Winter, David Ganley, Austen R. D. Leuchtmann, Adrian Young, Carolyn A. Cox, Murray P. |
author_facet | Quenu, Mathieu Treindl, Artemis D. Lee, Kate Takemoto, Daigo Thünen, Torsten Ashrafi, Samad Winter, David Ganley, Austen R. D. Leuchtmann, Adrian Young, Carolyn A. Cox, Murray P. |
author_sort | Quenu, Mathieu |
collection | PubMed |
description | Genome rearrangements in filamentous fungi are prevalent but little is known about the modalities of their evolution, in part because few complete genomes are available within a single genus. To address this, we have generated and compared 15 complete telomere-to-telomere genomes across the phylogeny of a single genus of filamentous fungi, Epichloë. We find that the striking distinction between gene-rich and repeat-rich regions previously reported for isolated species is ubiquitous across the Epichloë genus. We built a species phylogeny from single-copy gene orthologs to provide a comparative framing to study chromosome composition and structural change through evolutionary time. All Epichloë genomes have exactly seven nuclear chromosomes, but despite this conserved ploidy, analyses reveal low synteny and substantial rearrangement of gene content across the genus. These rearrangements are highly lineage-dependent, with most occurring over short evolutionary distances, with long periods of structural stasis. Quantification of chromosomal rearrangements shows they are uncorrelated with numbers of substitutions and evolutionary distances, suggesting that different modes of evolution are acting to create nucleotide and chromosome-scale changes. |
format | Online Article Text |
id | pubmed-9318876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93188762022-07-27 Telomere-to-Telomere Genome Sequences across a Single Genus Reveal Highly Variable Chromosome Rearrangement Rates but Absolute Stasis of Chromosome Number Quenu, Mathieu Treindl, Artemis D. Lee, Kate Takemoto, Daigo Thünen, Torsten Ashrafi, Samad Winter, David Ganley, Austen R. D. Leuchtmann, Adrian Young, Carolyn A. Cox, Murray P. J Fungi (Basel) Article Genome rearrangements in filamentous fungi are prevalent but little is known about the modalities of their evolution, in part because few complete genomes are available within a single genus. To address this, we have generated and compared 15 complete telomere-to-telomere genomes across the phylogeny of a single genus of filamentous fungi, Epichloë. We find that the striking distinction between gene-rich and repeat-rich regions previously reported for isolated species is ubiquitous across the Epichloë genus. We built a species phylogeny from single-copy gene orthologs to provide a comparative framing to study chromosome composition and structural change through evolutionary time. All Epichloë genomes have exactly seven nuclear chromosomes, but despite this conserved ploidy, analyses reveal low synteny and substantial rearrangement of gene content across the genus. These rearrangements are highly lineage-dependent, with most occurring over short evolutionary distances, with long periods of structural stasis. Quantification of chromosomal rearrangements shows they are uncorrelated with numbers of substitutions and evolutionary distances, suggesting that different modes of evolution are acting to create nucleotide and chromosome-scale changes. MDPI 2022-06-25 /pmc/articles/PMC9318876/ /pubmed/35887427 http://dx.doi.org/10.3390/jof8070670 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Quenu, Mathieu Treindl, Artemis D. Lee, Kate Takemoto, Daigo Thünen, Torsten Ashrafi, Samad Winter, David Ganley, Austen R. D. Leuchtmann, Adrian Young, Carolyn A. Cox, Murray P. Telomere-to-Telomere Genome Sequences across a Single Genus Reveal Highly Variable Chromosome Rearrangement Rates but Absolute Stasis of Chromosome Number |
title | Telomere-to-Telomere Genome Sequences across a Single Genus Reveal Highly Variable Chromosome Rearrangement Rates but Absolute Stasis of Chromosome Number |
title_full | Telomere-to-Telomere Genome Sequences across a Single Genus Reveal Highly Variable Chromosome Rearrangement Rates but Absolute Stasis of Chromosome Number |
title_fullStr | Telomere-to-Telomere Genome Sequences across a Single Genus Reveal Highly Variable Chromosome Rearrangement Rates but Absolute Stasis of Chromosome Number |
title_full_unstemmed | Telomere-to-Telomere Genome Sequences across a Single Genus Reveal Highly Variable Chromosome Rearrangement Rates but Absolute Stasis of Chromosome Number |
title_short | Telomere-to-Telomere Genome Sequences across a Single Genus Reveal Highly Variable Chromosome Rearrangement Rates but Absolute Stasis of Chromosome Number |
title_sort | telomere-to-telomere genome sequences across a single genus reveal highly variable chromosome rearrangement rates but absolute stasis of chromosome number |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9318876/ https://www.ncbi.nlm.nih.gov/pubmed/35887427 http://dx.doi.org/10.3390/jof8070670 |
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