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Limited mitogenomic degradation in response to a parasitic lifestyle in Orobanchaceae
In parasitic plants, the reduction in plastid genome (plastome) size and content is driven predominantly by the loss of photosynthetic genes. The first completed mitochondrial genomes (mitogenomes) from parasitic mistletoes also exhibit significant degradation, but the generality of this observation...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5093741/ https://www.ncbi.nlm.nih.gov/pubmed/27808159 http://dx.doi.org/10.1038/srep36285 |
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author | Fan, Weishu Zhu, Andan Kozaczek, Melisa Shah, Neethu Pabón-Mora, Natalia González, Favio Mower, Jeffrey P. |
author_facet | Fan, Weishu Zhu, Andan Kozaczek, Melisa Shah, Neethu Pabón-Mora, Natalia González, Favio Mower, Jeffrey P. |
author_sort | Fan, Weishu |
collection | PubMed |
description | In parasitic plants, the reduction in plastid genome (plastome) size and content is driven predominantly by the loss of photosynthetic genes. The first completed mitochondrial genomes (mitogenomes) from parasitic mistletoes also exhibit significant degradation, but the generality of this observation for other parasitic plants is unclear. We sequenced the complete mitogenome and plastome of the hemiparasite Castilleja paramensis (Orobanchaceae) and compared them with additional holoparasitic, hemiparasitic and nonparasitic species from Orobanchaceae. Comparative mitogenomic analysis revealed minimal gene loss among the seven Orobanchaceae species, indicating the retention of typical mitochondrial function among Orobanchaceae species. Phylogenetic analysis demonstrated that the mobile cox1 intron was acquired vertically from a nonparasitic ancestor, arguing against a role for Orobanchaceae parasites in the horizontal acquisition or distribution of this intron. The C. paramensis plastome has retained nearly all genes except for the recent pseudogenization of four subunits of the NAD(P)H dehydrogenase complex, indicating a very early stage of plastome degradation. These results lend support to the notion that loss of ndh gene function is the first step of plastome degradation in the transition to a parasitic lifestyle. |
format | Online Article Text |
id | pubmed-5093741 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50937412016-11-10 Limited mitogenomic degradation in response to a parasitic lifestyle in Orobanchaceae Fan, Weishu Zhu, Andan Kozaczek, Melisa Shah, Neethu Pabón-Mora, Natalia González, Favio Mower, Jeffrey P. Sci Rep Article In parasitic plants, the reduction in plastid genome (plastome) size and content is driven predominantly by the loss of photosynthetic genes. The first completed mitochondrial genomes (mitogenomes) from parasitic mistletoes also exhibit significant degradation, but the generality of this observation for other parasitic plants is unclear. We sequenced the complete mitogenome and plastome of the hemiparasite Castilleja paramensis (Orobanchaceae) and compared them with additional holoparasitic, hemiparasitic and nonparasitic species from Orobanchaceae. Comparative mitogenomic analysis revealed minimal gene loss among the seven Orobanchaceae species, indicating the retention of typical mitochondrial function among Orobanchaceae species. Phylogenetic analysis demonstrated that the mobile cox1 intron was acquired vertically from a nonparasitic ancestor, arguing against a role for Orobanchaceae parasites in the horizontal acquisition or distribution of this intron. The C. paramensis plastome has retained nearly all genes except for the recent pseudogenization of four subunits of the NAD(P)H dehydrogenase complex, indicating a very early stage of plastome degradation. These results lend support to the notion that loss of ndh gene function is the first step of plastome degradation in the transition to a parasitic lifestyle. Nature Publishing Group 2016-11-03 /pmc/articles/PMC5093741/ /pubmed/27808159 http://dx.doi.org/10.1038/srep36285 Text en Copyright © 2016, The Author(s) 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 Fan, Weishu Zhu, Andan Kozaczek, Melisa Shah, Neethu Pabón-Mora, Natalia González, Favio Mower, Jeffrey P. Limited mitogenomic degradation in response to a parasitic lifestyle in Orobanchaceae |
title | Limited mitogenomic degradation in response to a parasitic lifestyle in Orobanchaceae |
title_full | Limited mitogenomic degradation in response to a parasitic lifestyle in Orobanchaceae |
title_fullStr | Limited mitogenomic degradation in response to a parasitic lifestyle in Orobanchaceae |
title_full_unstemmed | Limited mitogenomic degradation in response to a parasitic lifestyle in Orobanchaceae |
title_short | Limited mitogenomic degradation in response to a parasitic lifestyle in Orobanchaceae |
title_sort | limited mitogenomic degradation in response to a parasitic lifestyle in orobanchaceae |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5093741/ https://www.ncbi.nlm.nih.gov/pubmed/27808159 http://dx.doi.org/10.1038/srep36285 |
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