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Plastome Structural Evolution and Homoplastic Inversions in Neo-Astragalus (Fabaceae)

The plastid genomes of photosynthetic green plants have largely maintained conserved gene content and order as well as structure over hundreds of millions of years of evolution. Several plant lineages, however, have departed from this conservation and contain many plastome structural rearrangements,...

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Detalles Bibliográficos
Autores principales: Charboneau, Joseph L M, Cronn, Richard C, Liston, Aaron, Wojciechowski, Martin F, Sanderson, Michael J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8486006/
https://www.ncbi.nlm.nih.gov/pubmed/34534296
http://dx.doi.org/10.1093/gbe/evab215
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author Charboneau, Joseph L M
Cronn, Richard C
Liston, Aaron
Wojciechowski, Martin F
Sanderson, Michael J
author_facet Charboneau, Joseph L M
Cronn, Richard C
Liston, Aaron
Wojciechowski, Martin F
Sanderson, Michael J
author_sort Charboneau, Joseph L M
collection PubMed
description The plastid genomes of photosynthetic green plants have largely maintained conserved gene content and order as well as structure over hundreds of millions of years of evolution. Several plant lineages, however, have departed from this conservation and contain many plastome structural rearrangements, which have been associated with an abundance of repeated sequences both overall and near rearrangement endpoints. We sequenced the plastomes of 25 taxa of Astragalus L. (Fabaceae), a large genus in the inverted repeat-lacking clade of legumes, to gain a greater understanding of the connection between repeats and plastome inversions. We found plastome repeat structure has a strong phylogenetic signal among these closely related taxa mostly in the New World clade of Astragalus called Neo-Astragalus. Taxa without inversions also do not differ substantially in their overall repeat structure from four taxa each with one large-scale inversion. For two taxa with inversion endpoints between the same pairs of genes, differences in their exact endpoints indicate the inversions occurred independently. Our proposed mechanism for inversion formation suggests the short inverted repeats now found near the endpoints of the four inversions may be there as a result of these inversions rather than their cause. The longer inverted repeats now near endpoints may have allowed the inversions first mediated by shorter microhomologous sequences to propagate, something that should be considered in explaining how any plastome rearrangement becomes fixed regardless of the mechanism of initial formation.
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spelling pubmed-84860062021-10-04 Plastome Structural Evolution and Homoplastic Inversions in Neo-Astragalus (Fabaceae) Charboneau, Joseph L M Cronn, Richard C Liston, Aaron Wojciechowski, Martin F Sanderson, Michael J Genome Biol Evol Research Article The plastid genomes of photosynthetic green plants have largely maintained conserved gene content and order as well as structure over hundreds of millions of years of evolution. Several plant lineages, however, have departed from this conservation and contain many plastome structural rearrangements, which have been associated with an abundance of repeated sequences both overall and near rearrangement endpoints. We sequenced the plastomes of 25 taxa of Astragalus L. (Fabaceae), a large genus in the inverted repeat-lacking clade of legumes, to gain a greater understanding of the connection between repeats and plastome inversions. We found plastome repeat structure has a strong phylogenetic signal among these closely related taxa mostly in the New World clade of Astragalus called Neo-Astragalus. Taxa without inversions also do not differ substantially in their overall repeat structure from four taxa each with one large-scale inversion. For two taxa with inversion endpoints between the same pairs of genes, differences in their exact endpoints indicate the inversions occurred independently. Our proposed mechanism for inversion formation suggests the short inverted repeats now found near the endpoints of the four inversions may be there as a result of these inversions rather than their cause. The longer inverted repeats now near endpoints may have allowed the inversions first mediated by shorter microhomologous sequences to propagate, something that should be considered in explaining how any plastome rearrangement becomes fixed regardless of the mechanism of initial formation. Oxford University Press 2021-09-17 /pmc/articles/PMC8486006/ /pubmed/34534296 http://dx.doi.org/10.1093/gbe/evab215 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Charboneau, Joseph L M
Cronn, Richard C
Liston, Aaron
Wojciechowski, Martin F
Sanderson, Michael J
Plastome Structural Evolution and Homoplastic Inversions in Neo-Astragalus (Fabaceae)
title Plastome Structural Evolution and Homoplastic Inversions in Neo-Astragalus (Fabaceae)
title_full Plastome Structural Evolution and Homoplastic Inversions in Neo-Astragalus (Fabaceae)
title_fullStr Plastome Structural Evolution and Homoplastic Inversions in Neo-Astragalus (Fabaceae)
title_full_unstemmed Plastome Structural Evolution and Homoplastic Inversions in Neo-Astragalus (Fabaceae)
title_short Plastome Structural Evolution and Homoplastic Inversions in Neo-Astragalus (Fabaceae)
title_sort plastome structural evolution and homoplastic inversions in neo-astragalus (fabaceae)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8486006/
https://www.ncbi.nlm.nih.gov/pubmed/34534296
http://dx.doi.org/10.1093/gbe/evab215
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