Cargando…

Mycoheterotrophic Epirixanthes (Polygalaceae) has a typical angiosperm mitogenome but unorthodox plastid genomes

BACKGROUND AND AIMS: Fully mycoheterotrophic plants derive carbon and other nutrients from root-associated fungi and have lost the ability to photosynthesize. While mycoheterotroph plastomes are often degraded compared with green plants, the effect of this unusual symbiosis on mitochondrial genome e...

Descripción completa

Detalles Bibliográficos
Autores principales: Petersen, G, Darby, H, Lam, V K Y, Pedersen, H Æ, Merckx, V S F T, Zervas, A, Seberg, O, Graham, S W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868387/
https://www.ncbi.nlm.nih.gov/pubmed/31346602
http://dx.doi.org/10.1093/aob/mcz114
_version_ 1783472247558635520
author Petersen, G
Darby, H
Lam, V K Y
Pedersen, H Æ
Merckx, V S F T
Zervas, A
Seberg, O
Graham, S W
author_facet Petersen, G
Darby, H
Lam, V K Y
Pedersen, H Æ
Merckx, V S F T
Zervas, A
Seberg, O
Graham, S W
author_sort Petersen, G
collection PubMed
description BACKGROUND AND AIMS: Fully mycoheterotrophic plants derive carbon and other nutrients from root-associated fungi and have lost the ability to photosynthesize. While mycoheterotroph plastomes are often degraded compared with green plants, the effect of this unusual symbiosis on mitochondrial genome evolution is unknown. By providing the first complete organelle genome data from Polygalaceae, one of only three eudicot families that developed mycoheterotrophy, we explore how both organellar genomes evolved after loss of photosynthesis. METHODS: We sequenced and assembled four complete plastid genomes and a mitochondrial genome from species of Polygalaceae, focusing on non-photosynthetic Epirixanthes. We compared these genomes with those of other mycoheterotroph and parasitic plant lineages, and assessed whether organelle genes in Epirixanthes experienced relaxed or intensified selection compared with autotrophic relatives. KEY RESULTS: Plastomes of two species of Epirixanthes have become substantially degraded compared with that of autotrophic Polygala. Although the lack of photosynthesis is presumably homologous in the genus, the surveyed Epirixanthes species have marked differences in terms of plastome size, structural rearrangements, gene content and substitution rates. Remarkably, both apparently replaced a canonical plastid inverted repeat with large directly repeated sequences. The mitogenome of E. elongata incorporated a considerable number of fossilized plastid genes, by intracellular transfer from an ancestor with a less degraded plastome. Both plastid and mitochondrial genes in E. elongata have increased substitution rates, but the plastid genes of E. pallida do not. Despite this, both species have similar selection patterns operating on plastid housekeeping genes. CONCLUSIONS: Plastome evolution largely fits with patterns of gene degradation seen in other heterotrophic plants, but includes highly unusual directly duplicated regions. The causes of rate elevation in the sequenced Epirixanthes mitogenome and of rate differences in plastomes of related mycoheterotrophic species are not currently understood.
format Online
Article
Text
id pubmed-6868387
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-68683872019-11-27 Mycoheterotrophic Epirixanthes (Polygalaceae) has a typical angiosperm mitogenome but unorthodox plastid genomes Petersen, G Darby, H Lam, V K Y Pedersen, H Æ Merckx, V S F T Zervas, A Seberg, O Graham, S W Ann Bot Original Articles BACKGROUND AND AIMS: Fully mycoheterotrophic plants derive carbon and other nutrients from root-associated fungi and have lost the ability to photosynthesize. While mycoheterotroph plastomes are often degraded compared with green plants, the effect of this unusual symbiosis on mitochondrial genome evolution is unknown. By providing the first complete organelle genome data from Polygalaceae, one of only three eudicot families that developed mycoheterotrophy, we explore how both organellar genomes evolved after loss of photosynthesis. METHODS: We sequenced and assembled four complete plastid genomes and a mitochondrial genome from species of Polygalaceae, focusing on non-photosynthetic Epirixanthes. We compared these genomes with those of other mycoheterotroph and parasitic plant lineages, and assessed whether organelle genes in Epirixanthes experienced relaxed or intensified selection compared with autotrophic relatives. KEY RESULTS: Plastomes of two species of Epirixanthes have become substantially degraded compared with that of autotrophic Polygala. Although the lack of photosynthesis is presumably homologous in the genus, the surveyed Epirixanthes species have marked differences in terms of plastome size, structural rearrangements, gene content and substitution rates. Remarkably, both apparently replaced a canonical plastid inverted repeat with large directly repeated sequences. The mitogenome of E. elongata incorporated a considerable number of fossilized plastid genes, by intracellular transfer from an ancestor with a less degraded plastome. Both plastid and mitochondrial genes in E. elongata have increased substitution rates, but the plastid genes of E. pallida do not. Despite this, both species have similar selection patterns operating on plastid housekeeping genes. CONCLUSIONS: Plastome evolution largely fits with patterns of gene degradation seen in other heterotrophic plants, but includes highly unusual directly duplicated regions. The causes of rate elevation in the sequenced Epirixanthes mitogenome and of rate differences in plastomes of related mycoheterotrophic species are not currently understood. Oxford University Press 2019-11 2019-07-26 /pmc/articles/PMC6868387/ /pubmed/31346602 http://dx.doi.org/10.1093/aob/mcz114 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Annals of Botany Company. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Petersen, G
Darby, H
Lam, V K Y
Pedersen, H Æ
Merckx, V S F T
Zervas, A
Seberg, O
Graham, S W
Mycoheterotrophic Epirixanthes (Polygalaceae) has a typical angiosperm mitogenome but unorthodox plastid genomes
title Mycoheterotrophic Epirixanthes (Polygalaceae) has a typical angiosperm mitogenome but unorthodox plastid genomes
title_full Mycoheterotrophic Epirixanthes (Polygalaceae) has a typical angiosperm mitogenome but unorthodox plastid genomes
title_fullStr Mycoheterotrophic Epirixanthes (Polygalaceae) has a typical angiosperm mitogenome but unorthodox plastid genomes
title_full_unstemmed Mycoheterotrophic Epirixanthes (Polygalaceae) has a typical angiosperm mitogenome but unorthodox plastid genomes
title_short Mycoheterotrophic Epirixanthes (Polygalaceae) has a typical angiosperm mitogenome but unorthodox plastid genomes
title_sort mycoheterotrophic epirixanthes (polygalaceae) has a typical angiosperm mitogenome but unorthodox plastid genomes
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868387/
https://www.ncbi.nlm.nih.gov/pubmed/31346602
http://dx.doi.org/10.1093/aob/mcz114
work_keys_str_mv AT peterseng mycoheterotrophicepirixanthespolygalaceaehasatypicalangiospermmitogenomebutunorthodoxplastidgenomes
AT darbyh mycoheterotrophicepirixanthespolygalaceaehasatypicalangiospermmitogenomebutunorthodoxplastidgenomes
AT lamvky mycoheterotrophicepirixanthespolygalaceaehasatypicalangiospermmitogenomebutunorthodoxplastidgenomes
AT pedersenhæ mycoheterotrophicepirixanthespolygalaceaehasatypicalangiospermmitogenomebutunorthodoxplastidgenomes
AT merckxvsft mycoheterotrophicepirixanthespolygalaceaehasatypicalangiospermmitogenomebutunorthodoxplastidgenomes
AT zervasa mycoheterotrophicepirixanthespolygalaceaehasatypicalangiospermmitogenomebutunorthodoxplastidgenomes
AT sebergo mycoheterotrophicepirixanthespolygalaceaehasatypicalangiospermmitogenomebutunorthodoxplastidgenomes
AT grahamsw mycoheterotrophicepirixanthespolygalaceaehasatypicalangiospermmitogenomebutunorthodoxplastidgenomes