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Structural Plastome Evolution in Holoparasitic Hydnoraceae with Special Focus on Inverted and Direct Repeats

Plastome condensation during adaptation to a heterotrophic lifestyle is generally well understood and lineage-independent models have been derived. However, understanding the evolutionary trajectories of comparatively old heterotrophic lineages that are on the cusp of a minimal plastome, is essentia...

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Autores principales: Jost, Matthias, Naumann, Julia, Bolin, Jay F., Martel, Carlos, Rocamundi, Nicolás, Cocucci, Andrea A., Lupton, Darach, Neinhuis, Christoph, Wanke, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9168662/
https://www.ncbi.nlm.nih.gov/pubmed/35660863
http://dx.doi.org/10.1093/gbe/evac077
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author Jost, Matthias
Naumann, Julia
Bolin, Jay F.
Martel, Carlos
Rocamundi, Nicolás
Cocucci, Andrea A.
Lupton, Darach
Neinhuis, Christoph
Wanke, Stefan
author_facet Jost, Matthias
Naumann, Julia
Bolin, Jay F.
Martel, Carlos
Rocamundi, Nicolás
Cocucci, Andrea A.
Lupton, Darach
Neinhuis, Christoph
Wanke, Stefan
author_sort Jost, Matthias
collection PubMed
description Plastome condensation during adaptation to a heterotrophic lifestyle is generally well understood and lineage-independent models have been derived. However, understanding the evolutionary trajectories of comparatively old heterotrophic lineages that are on the cusp of a minimal plastome, is essential to complement and expand current knowledge. We study Hydnoraceae, one of the oldest and least investigated parasitic angiosperm lineages. Plastome comparative genomics, using seven out of eight known species of the genus Hydnora and three species of Prosopanche, reveal a high degree of structural similarity and shared gene content; contrasted by striking dissimilarities with respect to repeat content [inverted and direct repeats (DRs)]. We identified varying inverted repeat contents and positions, likely resulting from multiple, independent evolutionary events, and a DR gain in Prosopanche. Considering different evolutionary trajectories and based on a fully resolved and supported species-level phylogenetic hypothesis, we describe three possible, distinct models to explain the Hydnoraceae plastome states. For comparative purposes, we also report the first plastid genomes for the closely related autotrophic genera Lactoris (Lactoridaceae) and Thottea (Aristolochiaceae).
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spelling pubmed-91686622022-06-06 Structural Plastome Evolution in Holoparasitic Hydnoraceae with Special Focus on Inverted and Direct Repeats Jost, Matthias Naumann, Julia Bolin, Jay F. Martel, Carlos Rocamundi, Nicolás Cocucci, Andrea A. Lupton, Darach Neinhuis, Christoph Wanke, Stefan Genome Biol Evol Research Article Plastome condensation during adaptation to a heterotrophic lifestyle is generally well understood and lineage-independent models have been derived. However, understanding the evolutionary trajectories of comparatively old heterotrophic lineages that are on the cusp of a minimal plastome, is essential to complement and expand current knowledge. We study Hydnoraceae, one of the oldest and least investigated parasitic angiosperm lineages. Plastome comparative genomics, using seven out of eight known species of the genus Hydnora and three species of Prosopanche, reveal a high degree of structural similarity and shared gene content; contrasted by striking dissimilarities with respect to repeat content [inverted and direct repeats (DRs)]. We identified varying inverted repeat contents and positions, likely resulting from multiple, independent evolutionary events, and a DR gain in Prosopanche. Considering different evolutionary trajectories and based on a fully resolved and supported species-level phylogenetic hypothesis, we describe three possible, distinct models to explain the Hydnoraceae plastome states. For comparative purposes, we also report the first plastid genomes for the closely related autotrophic genera Lactoris (Lactoridaceae) and Thottea (Aristolochiaceae). Oxford University Press 2022-05-25 /pmc/articles/PMC9168662/ /pubmed/35660863 http://dx.doi.org/10.1093/gbe/evac077 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Jost, Matthias
Naumann, Julia
Bolin, Jay F.
Martel, Carlos
Rocamundi, Nicolás
Cocucci, Andrea A.
Lupton, Darach
Neinhuis, Christoph
Wanke, Stefan
Structural Plastome Evolution in Holoparasitic Hydnoraceae with Special Focus on Inverted and Direct Repeats
title Structural Plastome Evolution in Holoparasitic Hydnoraceae with Special Focus on Inverted and Direct Repeats
title_full Structural Plastome Evolution in Holoparasitic Hydnoraceae with Special Focus on Inverted and Direct Repeats
title_fullStr Structural Plastome Evolution in Holoparasitic Hydnoraceae with Special Focus on Inverted and Direct Repeats
title_full_unstemmed Structural Plastome Evolution in Holoparasitic Hydnoraceae with Special Focus on Inverted and Direct Repeats
title_short Structural Plastome Evolution in Holoparasitic Hydnoraceae with Special Focus on Inverted and Direct Repeats
title_sort structural plastome evolution in holoparasitic hydnoraceae with special focus on inverted and direct repeats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9168662/
https://www.ncbi.nlm.nih.gov/pubmed/35660863
http://dx.doi.org/10.1093/gbe/evac077
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