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Mitochondrial genome evolution in parasitic plants
BACKGROUND: Parasitic plants rely on their host to cover their nutritional requirements either for their entire life or a smaller part of it. Depending on the level of parasitism, a proportional reduction on the plastid genome has been found. However, knowledge on gene loss and evolution of the mito...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6454704/ https://www.ncbi.nlm.nih.gov/pubmed/30961535 http://dx.doi.org/10.1186/s12862-019-1401-8 |
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author | Zervas, Athanasios Petersen, Gitte Seberg, Ole |
author_facet | Zervas, Athanasios Petersen, Gitte Seberg, Ole |
author_sort | Zervas, Athanasios |
collection | PubMed |
description | BACKGROUND: Parasitic plants rely on their host to cover their nutritional requirements either for their entire life or a smaller part of it. Depending on the level of parasitism, a proportional reduction on the plastid genome has been found. However, knowledge on gene loss and evolution of the mitogenome of parasitic plants is only available for four hemiparasitic Viscum species (Viscaceae), which lack many of the mitochondrial genes, while the remaining genes exhibit very fast molecular evolution rates. In this study, we include another genus, Phoradendron, from the Viscaceae, as well as 10 other hemiparasitic or holoparasitic taxa from across the phylogeny of the angiosperms to investigate how fast molecular evolution works on their mitogenomes, and the extent of gene loss. RESULTS: Our observations from Viscum were replicated in Phoradendron liga, whereas the remaining parasitic plants in the study have a complete set of the core mitochondrial genes and exhibit moderate or only slightly raised substitution rates compared to most autotrophic taxa, without any statistically significant difference between the different groups (autotrophs, hemiparasites and holoparasites). Additionally, further evidence is provided for the placement of Balanophoraceae within the order Santalales, while the exact placement of Cynomoriaceae still remains elusive. CONCLUSIONS: We examine the mitochondrial gene content of 11 hemiparasitic and holoparasitic plants and confirm previous observations in Viscaceae. We show that the remaining parasitic plants do not have significantly higher substitution rates than autotrophic plants in their mitochondrial genes. We provide further evidence for the placement of Balanophoraceae in the Santalales. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-019-1401-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6454704 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64547042019-04-19 Mitochondrial genome evolution in parasitic plants Zervas, Athanasios Petersen, Gitte Seberg, Ole BMC Evol Biol Research Article BACKGROUND: Parasitic plants rely on their host to cover their nutritional requirements either for their entire life or a smaller part of it. Depending on the level of parasitism, a proportional reduction on the plastid genome has been found. However, knowledge on gene loss and evolution of the mitogenome of parasitic plants is only available for four hemiparasitic Viscum species (Viscaceae), which lack many of the mitochondrial genes, while the remaining genes exhibit very fast molecular evolution rates. In this study, we include another genus, Phoradendron, from the Viscaceae, as well as 10 other hemiparasitic or holoparasitic taxa from across the phylogeny of the angiosperms to investigate how fast molecular evolution works on their mitogenomes, and the extent of gene loss. RESULTS: Our observations from Viscum were replicated in Phoradendron liga, whereas the remaining parasitic plants in the study have a complete set of the core mitochondrial genes and exhibit moderate or only slightly raised substitution rates compared to most autotrophic taxa, without any statistically significant difference between the different groups (autotrophs, hemiparasites and holoparasites). Additionally, further evidence is provided for the placement of Balanophoraceae within the order Santalales, while the exact placement of Cynomoriaceae still remains elusive. CONCLUSIONS: We examine the mitochondrial gene content of 11 hemiparasitic and holoparasitic plants and confirm previous observations in Viscaceae. We show that the remaining parasitic plants do not have significantly higher substitution rates than autotrophic plants in their mitochondrial genes. We provide further evidence for the placement of Balanophoraceae in the Santalales. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-019-1401-8) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-08 /pmc/articles/PMC6454704/ /pubmed/30961535 http://dx.doi.org/10.1186/s12862-019-1401-8 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Zervas, Athanasios Petersen, Gitte Seberg, Ole Mitochondrial genome evolution in parasitic plants |
title | Mitochondrial genome evolution in parasitic plants |
title_full | Mitochondrial genome evolution in parasitic plants |
title_fullStr | Mitochondrial genome evolution in parasitic plants |
title_full_unstemmed | Mitochondrial genome evolution in parasitic plants |
title_short | Mitochondrial genome evolution in parasitic plants |
title_sort | mitochondrial genome evolution in parasitic plants |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6454704/ https://www.ncbi.nlm.nih.gov/pubmed/30961535 http://dx.doi.org/10.1186/s12862-019-1401-8 |
work_keys_str_mv | AT zervasathanasios mitochondrialgenomeevolutioninparasiticplants AT petersengitte mitochondrialgenomeevolutioninparasiticplants AT sebergole mitochondrialgenomeevolutioninparasiticplants |