Cargando…
Pangenomic Analysis of Nucleo-Cytoplasmic Large DNA Viruses. I: The Phylogenetic Distribution of Conserved Oxygen-Dependent Enzymes Reveals a Capture-Gene Process
The Nucleo-Cytoplasmic Large DNA Viruses (NCLDVs) infect a wide range of eukaryotic species, including amoeba, algae, fish, amphibia, arthropods, birds, and mammals. This group of viruses has linear or circular double-stranded DNA genomes whose size spans approximately one order of magnitude, from 1...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10598087/ https://www.ncbi.nlm.nih.gov/pubmed/37526693 http://dx.doi.org/10.1007/s00239-023-10126-z |
_version_ | 1785125476866457600 |
---|---|
author | Campillo-Balderas, J. A. Lazcano, A. Cottom-Salas, W. Jácome, R. Becerra, A. |
author_facet | Campillo-Balderas, J. A. Lazcano, A. Cottom-Salas, W. Jácome, R. Becerra, A. |
author_sort | Campillo-Balderas, J. A. |
collection | PubMed |
description | The Nucleo-Cytoplasmic Large DNA Viruses (NCLDVs) infect a wide range of eukaryotic species, including amoeba, algae, fish, amphibia, arthropods, birds, and mammals. This group of viruses has linear or circular double-stranded DNA genomes whose size spans approximately one order of magnitude, from 100 to 2500 kbp. The ultimate origin of this peculiar group of viruses remains an open issue. Some have argued that NCLDVs’ origin may lie in a bacteriophage ancestor that increased its genome size by subsequent recruitment of eukaryotic and bacterial genes. Others have suggested that NCLDVs families originated from cells that underwent an irreversible process of genome reduction. However, the hypothesis that a number of NCLDVs sequences have been recruited from the host genomes has been largely ignored. In the present work, we have performed pangenomic analyses of each of the seven known NCLDVs families. We show that these families' core- and shell genes have cellular homologs, supporting possible escaping-gene events as part of its evolution. Furthermore, the detection of sequences that belong to two protein families (small chain ribonucleotide reductase and Erv1/Air) and to one superfamily [2OG-Fe(II) oxygenases] that are for distribution in all NCLDVs core and shell clusters encoding for oxygen-dependent enzymes suggests that the highly conserved core these viruses originated after the Proterozoic Great Oxidation Event that transformed the terrestrial atmosphere 2.4–2.3 Ga ago. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00239-023-10126-z. |
format | Online Article Text |
id | pubmed-10598087 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-105980872023-10-26 Pangenomic Analysis of Nucleo-Cytoplasmic Large DNA Viruses. I: The Phylogenetic Distribution of Conserved Oxygen-Dependent Enzymes Reveals a Capture-Gene Process Campillo-Balderas, J. A. Lazcano, A. Cottom-Salas, W. Jácome, R. Becerra, A. J Mol Evol Original Article The Nucleo-Cytoplasmic Large DNA Viruses (NCLDVs) infect a wide range of eukaryotic species, including amoeba, algae, fish, amphibia, arthropods, birds, and mammals. This group of viruses has linear or circular double-stranded DNA genomes whose size spans approximately one order of magnitude, from 100 to 2500 kbp. The ultimate origin of this peculiar group of viruses remains an open issue. Some have argued that NCLDVs’ origin may lie in a bacteriophage ancestor that increased its genome size by subsequent recruitment of eukaryotic and bacterial genes. Others have suggested that NCLDVs families originated from cells that underwent an irreversible process of genome reduction. However, the hypothesis that a number of NCLDVs sequences have been recruited from the host genomes has been largely ignored. In the present work, we have performed pangenomic analyses of each of the seven known NCLDVs families. We show that these families' core- and shell genes have cellular homologs, supporting possible escaping-gene events as part of its evolution. Furthermore, the detection of sequences that belong to two protein families (small chain ribonucleotide reductase and Erv1/Air) and to one superfamily [2OG-Fe(II) oxygenases] that are for distribution in all NCLDVs core and shell clusters encoding for oxygen-dependent enzymes suggests that the highly conserved core these viruses originated after the Proterozoic Great Oxidation Event that transformed the terrestrial atmosphere 2.4–2.3 Ga ago. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00239-023-10126-z. Springer US 2023-08-01 2023 /pmc/articles/PMC10598087/ /pubmed/37526693 http://dx.doi.org/10.1007/s00239-023-10126-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Campillo-Balderas, J. A. Lazcano, A. Cottom-Salas, W. Jácome, R. Becerra, A. Pangenomic Analysis of Nucleo-Cytoplasmic Large DNA Viruses. I: The Phylogenetic Distribution of Conserved Oxygen-Dependent Enzymes Reveals a Capture-Gene Process |
title | Pangenomic Analysis of Nucleo-Cytoplasmic Large DNA Viruses. I: The Phylogenetic Distribution of Conserved Oxygen-Dependent Enzymes Reveals a Capture-Gene Process |
title_full | Pangenomic Analysis of Nucleo-Cytoplasmic Large DNA Viruses. I: The Phylogenetic Distribution of Conserved Oxygen-Dependent Enzymes Reveals a Capture-Gene Process |
title_fullStr | Pangenomic Analysis of Nucleo-Cytoplasmic Large DNA Viruses. I: The Phylogenetic Distribution of Conserved Oxygen-Dependent Enzymes Reveals a Capture-Gene Process |
title_full_unstemmed | Pangenomic Analysis of Nucleo-Cytoplasmic Large DNA Viruses. I: The Phylogenetic Distribution of Conserved Oxygen-Dependent Enzymes Reveals a Capture-Gene Process |
title_short | Pangenomic Analysis of Nucleo-Cytoplasmic Large DNA Viruses. I: The Phylogenetic Distribution of Conserved Oxygen-Dependent Enzymes Reveals a Capture-Gene Process |
title_sort | pangenomic analysis of nucleo-cytoplasmic large dna viruses. i: the phylogenetic distribution of conserved oxygen-dependent enzymes reveals a capture-gene process |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10598087/ https://www.ncbi.nlm.nih.gov/pubmed/37526693 http://dx.doi.org/10.1007/s00239-023-10126-z |
work_keys_str_mv | AT campillobalderasja pangenomicanalysisofnucleocytoplasmiclargednavirusesithephylogeneticdistributionofconservedoxygendependentenzymesrevealsacapturegeneprocess AT lazcanoa pangenomicanalysisofnucleocytoplasmiclargednavirusesithephylogeneticdistributionofconservedoxygendependentenzymesrevealsacapturegeneprocess AT cottomsalasw pangenomicanalysisofnucleocytoplasmiclargednavirusesithephylogeneticdistributionofconservedoxygendependentenzymesrevealsacapturegeneprocess AT jacomer pangenomicanalysisofnucleocytoplasmiclargednavirusesithephylogeneticdistributionofconservedoxygendependentenzymesrevealsacapturegeneprocess AT becerraa pangenomicanalysisofnucleocytoplasmiclargednavirusesithephylogeneticdistributionofconservedoxygendependentenzymesrevealsacapturegeneprocess |