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Massive gene loss in mistletoe (Viscum, Viscaceae) mitochondria
Parasitism is a successful survival strategy across all kingdoms and has evolved repeatedly in angiosperms. Parasitic plants obtain nutrients from other plants and some are agricultural pests. Obligate parasites, which cannot complete their lifecycle without a host, may lack functional photosystems...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667250/ https://www.ncbi.nlm.nih.gov/pubmed/26625950 http://dx.doi.org/10.1038/srep17588 |
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author | Petersen, G. Cuenca, A. Møller, I. M. Seberg, O. |
author_facet | Petersen, G. Cuenca, A. Møller, I. M. Seberg, O. |
author_sort | Petersen, G. |
collection | PubMed |
description | Parasitism is a successful survival strategy across all kingdoms and has evolved repeatedly in angiosperms. Parasitic plants obtain nutrients from other plants and some are agricultural pests. Obligate parasites, which cannot complete their lifecycle without a host, may lack functional photosystems (holoparasites), or have retained photosynthesis (hemiparasites). Plastid genomes are often reduced in parasites, but complete mitochondrial genomes have not been sequenced and their mitochondrial respiratory capacities are largely unknown. The hemiparasitic European mistletoe (Viscum album), known from folklore and postulated therapeutic properties, is a pest in plantations and forestry. We compare the mitochondrial genomes of three Viscum species based on the complete mitochondrial genome of V. album, the first from a parasitic plant. We show that mitochondrial genes encoding proteins of all respiratory complexes are lacking or pseudogenized raising several questions relevant to all parasitic plants: Are any mitochondrial gene functions essential? Do any genes need to be located in the mitochondrial genome or can they all be transferred to the nucleus? Can parasitic plants survive without oxidative phosphorylation by using alternative respiratory pathways? More generally, our study is a step towards understanding how host- and self-perception, host integration and nucleic acid transfer has modified ancestral mitochondrial genomes. |
format | Online Article Text |
id | pubmed-4667250 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46672502015-12-08 Massive gene loss in mistletoe (Viscum, Viscaceae) mitochondria Petersen, G. Cuenca, A. Møller, I. M. Seberg, O. Sci Rep Article Parasitism is a successful survival strategy across all kingdoms and has evolved repeatedly in angiosperms. Parasitic plants obtain nutrients from other plants and some are agricultural pests. Obligate parasites, which cannot complete their lifecycle without a host, may lack functional photosystems (holoparasites), or have retained photosynthesis (hemiparasites). Plastid genomes are often reduced in parasites, but complete mitochondrial genomes have not been sequenced and their mitochondrial respiratory capacities are largely unknown. The hemiparasitic European mistletoe (Viscum album), known from folklore and postulated therapeutic properties, is a pest in plantations and forestry. We compare the mitochondrial genomes of three Viscum species based on the complete mitochondrial genome of V. album, the first from a parasitic plant. We show that mitochondrial genes encoding proteins of all respiratory complexes are lacking or pseudogenized raising several questions relevant to all parasitic plants: Are any mitochondrial gene functions essential? Do any genes need to be located in the mitochondrial genome or can they all be transferred to the nucleus? Can parasitic plants survive without oxidative phosphorylation by using alternative respiratory pathways? More generally, our study is a step towards understanding how host- and self-perception, host integration and nucleic acid transfer has modified ancestral mitochondrial genomes. Nature Publishing Group 2015-12-02 /pmc/articles/PMC4667250/ /pubmed/26625950 http://dx.doi.org/10.1038/srep17588 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Petersen, G. Cuenca, A. Møller, I. M. Seberg, O. Massive gene loss in mistletoe (Viscum, Viscaceae) mitochondria |
title | Massive gene loss in mistletoe (Viscum, Viscaceae) mitochondria |
title_full | Massive gene loss in mistletoe (Viscum, Viscaceae) mitochondria |
title_fullStr | Massive gene loss in mistletoe (Viscum, Viscaceae) mitochondria |
title_full_unstemmed | Massive gene loss in mistletoe (Viscum, Viscaceae) mitochondria |
title_short | Massive gene loss in mistletoe (Viscum, Viscaceae) mitochondria |
title_sort | massive gene loss in mistletoe (viscum, viscaceae) mitochondria |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667250/ https://www.ncbi.nlm.nih.gov/pubmed/26625950 http://dx.doi.org/10.1038/srep17588 |
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