Cargando…
The genomes of polyextremophilic cyanidiales contain 1% horizontally transferred genes with diverse adaptive functions
The role and extent of horizontal gene transfer (HGT) in eukaryotes are hotly disputed topics that impact our understanding of the origin of metabolic processes and the role of organelles in cellular evolution. We addressed this issue by analyzing 10 novel Cyanidiales genomes and determined that 1%...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629376/ https://www.ncbi.nlm.nih.gov/pubmed/31149898 http://dx.doi.org/10.7554/eLife.45017 |
_version_ | 1783435099018100736 |
---|---|
author | Rossoni, Alessandro W Price, Dana C Seger, Mark Lyska, Dagmar Lammers, Peter Bhattacharya, Debashish Weber, Andreas PM |
author_facet | Rossoni, Alessandro W Price, Dana C Seger, Mark Lyska, Dagmar Lammers, Peter Bhattacharya, Debashish Weber, Andreas PM |
author_sort | Rossoni, Alessandro W |
collection | PubMed |
description | The role and extent of horizontal gene transfer (HGT) in eukaryotes are hotly disputed topics that impact our understanding of the origin of metabolic processes and the role of organelles in cellular evolution. We addressed this issue by analyzing 10 novel Cyanidiales genomes and determined that 1% of their gene inventory is HGT-derived. Numerous HGT candidates share a close phylogenetic relationship with prokaryotes that live in similar habitats as the Cyanidiales and encode functions related to polyextremophily. HGT candidates differ from native genes in GC-content, number of splice sites, and gene expression. HGT candidates are more prone to loss, which may explain the absence of a eukaryotic pan-genome. Therefore, the lack of a pan-genome and cumulative effects fail to provide substantive arguments against our hypothesis of recurring HGT followed by differential loss in eukaryotes. The maintenance of 1% HGTs, even under selection for genome reduction, underlines the importance of non-endosymbiosis related foreign gene acquisition. |
format | Online Article Text |
id | pubmed-6629376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-66293762019-07-17 The genomes of polyextremophilic cyanidiales contain 1% horizontally transferred genes with diverse adaptive functions Rossoni, Alessandro W Price, Dana C Seger, Mark Lyska, Dagmar Lammers, Peter Bhattacharya, Debashish Weber, Andreas PM eLife Evolutionary Biology The role and extent of horizontal gene transfer (HGT) in eukaryotes are hotly disputed topics that impact our understanding of the origin of metabolic processes and the role of organelles in cellular evolution. We addressed this issue by analyzing 10 novel Cyanidiales genomes and determined that 1% of their gene inventory is HGT-derived. Numerous HGT candidates share a close phylogenetic relationship with prokaryotes that live in similar habitats as the Cyanidiales and encode functions related to polyextremophily. HGT candidates differ from native genes in GC-content, number of splice sites, and gene expression. HGT candidates are more prone to loss, which may explain the absence of a eukaryotic pan-genome. Therefore, the lack of a pan-genome and cumulative effects fail to provide substantive arguments against our hypothesis of recurring HGT followed by differential loss in eukaryotes. The maintenance of 1% HGTs, even under selection for genome reduction, underlines the importance of non-endosymbiosis related foreign gene acquisition. eLife Sciences Publications, Ltd 2019-05-31 /pmc/articles/PMC6629376/ /pubmed/31149898 http://dx.doi.org/10.7554/eLife.45017 Text en © 2019, Rossoni 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 | Evolutionary Biology Rossoni, Alessandro W Price, Dana C Seger, Mark Lyska, Dagmar Lammers, Peter Bhattacharya, Debashish Weber, Andreas PM The genomes of polyextremophilic cyanidiales contain 1% horizontally transferred genes with diverse adaptive functions |
title | The genomes of polyextremophilic cyanidiales contain 1% horizontally transferred genes with diverse adaptive functions |
title_full | The genomes of polyextremophilic cyanidiales contain 1% horizontally transferred genes with diverse adaptive functions |
title_fullStr | The genomes of polyextremophilic cyanidiales contain 1% horizontally transferred genes with diverse adaptive functions |
title_full_unstemmed | The genomes of polyextremophilic cyanidiales contain 1% horizontally transferred genes with diverse adaptive functions |
title_short | The genomes of polyextremophilic cyanidiales contain 1% horizontally transferred genes with diverse adaptive functions |
title_sort | genomes of polyextremophilic cyanidiales contain 1% horizontally transferred genes with diverse adaptive functions |
topic | Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629376/ https://www.ncbi.nlm.nih.gov/pubmed/31149898 http://dx.doi.org/10.7554/eLife.45017 |
work_keys_str_mv | AT rossonialessandrow thegenomesofpolyextremophiliccyanidialescontain1horizontallytransferredgeneswithdiverseadaptivefunctions AT pricedanac thegenomesofpolyextremophiliccyanidialescontain1horizontallytransferredgeneswithdiverseadaptivefunctions AT segermark thegenomesofpolyextremophiliccyanidialescontain1horizontallytransferredgeneswithdiverseadaptivefunctions AT lyskadagmar thegenomesofpolyextremophiliccyanidialescontain1horizontallytransferredgeneswithdiverseadaptivefunctions AT lammerspeter thegenomesofpolyextremophiliccyanidialescontain1horizontallytransferredgeneswithdiverseadaptivefunctions AT bhattacharyadebashish thegenomesofpolyextremophiliccyanidialescontain1horizontallytransferredgeneswithdiverseadaptivefunctions AT weberandreaspm thegenomesofpolyextremophiliccyanidialescontain1horizontallytransferredgeneswithdiverseadaptivefunctions AT rossonialessandrow genomesofpolyextremophiliccyanidialescontain1horizontallytransferredgeneswithdiverseadaptivefunctions AT pricedanac genomesofpolyextremophiliccyanidialescontain1horizontallytransferredgeneswithdiverseadaptivefunctions AT segermark genomesofpolyextremophiliccyanidialescontain1horizontallytransferredgeneswithdiverseadaptivefunctions AT lyskadagmar genomesofpolyextremophiliccyanidialescontain1horizontallytransferredgeneswithdiverseadaptivefunctions AT lammerspeter genomesofpolyextremophiliccyanidialescontain1horizontallytransferredgeneswithdiverseadaptivefunctions AT bhattacharyadebashish genomesofpolyextremophiliccyanidialescontain1horizontallytransferredgeneswithdiverseadaptivefunctions AT weberandreaspm genomesofpolyextremophiliccyanidialescontain1horizontallytransferredgeneswithdiverseadaptivefunctions |