Cargando…
Greater genetic and regulatory plasticity of retained duplicates in Epichloë endophytic fungi
Gene duplicates can act as a source of genetic material from which new functions arise. Most duplicated genes revert to single copy genes and only a small proportion are retained. However, it remains unclear why some duplicate genes persist in the genome for an extended time. We investigate this que...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004115/ https://www.ncbi.nlm.nih.gov/pubmed/31614039 http://dx.doi.org/10.1111/mec.15275 |
_version_ | 1783494665607053312 |
---|---|
author | Wu, Baojun Cox, Murray P. |
author_facet | Wu, Baojun Cox, Murray P. |
author_sort | Wu, Baojun |
collection | PubMed |
description | Gene duplicates can act as a source of genetic material from which new functions arise. Most duplicated genes revert to single copy genes and only a small proportion are retained. However, it remains unclear why some duplicate genes persist in the genome for an extended time. We investigate this question by analysing retained gene duplicates in the fungal genus Epichloë, ascomycete fungi that form close endophytic symbioses with their host grasses. Retained duplicates within this genus have two independent origins, but both long pre‐date the origin and diversification of the genus Epichloë. We find that loss of retained duplicates within the genus is frequent and often associated with speciation. Retained duplicates have faster evolutionary rates (Ka) and show relaxed selection (Ka/Ks) compared to single copy genes. Both features are time‐dependent. Through comparison of conspecific strains, we find greater evolutionary rates in coding regions and sequence divergence in regulatory regions of retained duplicates than single copy genes, with this pattern more pronounced for strains adapted to different grass host species. Consistent with this sequence divergence in regulatory regions, transcriptome analyses show greater expression variation of retained duplicates than single copy genes. This suggest that cis‐regulatory changes make important contributions to the expression patterns of retained duplicates. Coupled with supporting observations from the model yeast Saccharomyces cerevisiae, these data suggest that genetic robustness and regulatory plasticity are common drivers behind the retention of duplicated genes in fungi. |
format | Online Article Text |
id | pubmed-7004115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70041152020-02-11 Greater genetic and regulatory plasticity of retained duplicates in Epichloë endophytic fungi Wu, Baojun Cox, Murray P. Mol Ecol ORIGINAL ARTICLES Gene duplicates can act as a source of genetic material from which new functions arise. Most duplicated genes revert to single copy genes and only a small proportion are retained. However, it remains unclear why some duplicate genes persist in the genome for an extended time. We investigate this question by analysing retained gene duplicates in the fungal genus Epichloë, ascomycete fungi that form close endophytic symbioses with their host grasses. Retained duplicates within this genus have two independent origins, but both long pre‐date the origin and diversification of the genus Epichloë. We find that loss of retained duplicates within the genus is frequent and often associated with speciation. Retained duplicates have faster evolutionary rates (Ka) and show relaxed selection (Ka/Ks) compared to single copy genes. Both features are time‐dependent. Through comparison of conspecific strains, we find greater evolutionary rates in coding regions and sequence divergence in regulatory regions of retained duplicates than single copy genes, with this pattern more pronounced for strains adapted to different grass host species. Consistent with this sequence divergence in regulatory regions, transcriptome analyses show greater expression variation of retained duplicates than single copy genes. This suggest that cis‐regulatory changes make important contributions to the expression patterns of retained duplicates. Coupled with supporting observations from the model yeast Saccharomyces cerevisiae, these data suggest that genetic robustness and regulatory plasticity are common drivers behind the retention of duplicated genes in fungi. John Wiley and Sons Inc. 2019-11-06 2019-12 /pmc/articles/PMC7004115/ /pubmed/31614039 http://dx.doi.org/10.1111/mec.15275 Text en © 2019 The Authors. Molecular Ecology published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | ORIGINAL ARTICLES Wu, Baojun Cox, Murray P. Greater genetic and regulatory plasticity of retained duplicates in Epichloë endophytic fungi |
title | Greater genetic and regulatory plasticity of retained duplicates in Epichloë endophytic fungi |
title_full | Greater genetic and regulatory plasticity of retained duplicates in Epichloë endophytic fungi |
title_fullStr | Greater genetic and regulatory plasticity of retained duplicates in Epichloë endophytic fungi |
title_full_unstemmed | Greater genetic and regulatory plasticity of retained duplicates in Epichloë endophytic fungi |
title_short | Greater genetic and regulatory plasticity of retained duplicates in Epichloë endophytic fungi |
title_sort | greater genetic and regulatory plasticity of retained duplicates in epichloë endophytic fungi |
topic | ORIGINAL ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004115/ https://www.ncbi.nlm.nih.gov/pubmed/31614039 http://dx.doi.org/10.1111/mec.15275 |
work_keys_str_mv | AT wubaojun greatergeneticandregulatoryplasticityofretainedduplicatesinepichloeendophyticfungi AT coxmurrayp greatergeneticandregulatoryplasticityofretainedduplicatesinepichloeendophyticfungi |