Cargando…

Complete plastid genomes from Ophioglossum californicum, Psilotum nudum, and Equisetum hyemale reveal an ancestral land plant genome structure and resolve the position of Equisetales among monilophytes

BACKGROUND: Plastid genome structure and content is remarkably conserved in land plants. This widespread conservation has facilitated taxon-rich phylogenetic analyses that have resolved organismal relationships among many land plant groups. However, the relationships among major fern lineages, espec...

Descripción completa

Detalles Bibliográficos
Autores principales: Grewe, Felix, Guo, Wenhu, Gubbels, Emily A, Hansen, A Katie, Mower, Jeffrey P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3553075/
https://www.ncbi.nlm.nih.gov/pubmed/23311954
http://dx.doi.org/10.1186/1471-2148-13-8
_version_ 1782256779029118976
author Grewe, Felix
Guo, Wenhu
Gubbels, Emily A
Hansen, A Katie
Mower, Jeffrey P
author_facet Grewe, Felix
Guo, Wenhu
Gubbels, Emily A
Hansen, A Katie
Mower, Jeffrey P
author_sort Grewe, Felix
collection PubMed
description BACKGROUND: Plastid genome structure and content is remarkably conserved in land plants. This widespread conservation has facilitated taxon-rich phylogenetic analyses that have resolved organismal relationships among many land plant groups. However, the relationships among major fern lineages, especially the placement of Equisetales, remain enigmatic. RESULTS: In order to understand the evolution of plastid genomes and to establish phylogenetic relationships among ferns, we sequenced the plastid genomes from three early diverging species: Equisetum hyemale (Equisetales), Ophioglossum californicum (Ophioglossales), and Psilotum nudum (Psilotales). A comparison of fern plastid genomes showed that some lineages have retained inverted repeat (IR) boundaries originating from the common ancestor of land plants, while other lineages have experienced multiple IR changes including expansions and inversions. Genome content has remained stable throughout ferns, except for a few lineage-specific losses of genes and introns. Notably, the losses of the rps16 gene and the rps12i346 intron are shared among Psilotales, Ophioglossales, and Equisetales, while the gain of a mitochondrial atp1 intron is shared between Marattiales and Polypodiopsida. These genomic structural changes support the placement of Equisetales as sister to Ophioglossales + Psilotales and Marattiales as sister to Polypodiopsida. This result is augmented by some molecular phylogenetic analyses that recover the same relationships, whereas others suggest a relationship between Equisetales and Polypodiopsida. CONCLUSIONS: Although molecular analyses were inconsistent with respect to the position of Marattiales and Equisetales, several genomic structural changes have for the first time provided a clear placement of these lineages within the ferns. These results further demonstrate the power of using rare genomic structural changes in cases where molecular data fail to provide strong phylogenetic resolution.
format Online
Article
Text
id pubmed-3553075
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-35530752013-01-28 Complete plastid genomes from Ophioglossum californicum, Psilotum nudum, and Equisetum hyemale reveal an ancestral land plant genome structure and resolve the position of Equisetales among monilophytes Grewe, Felix Guo, Wenhu Gubbels, Emily A Hansen, A Katie Mower, Jeffrey P BMC Evol Biol Research Article BACKGROUND: Plastid genome structure and content is remarkably conserved in land plants. This widespread conservation has facilitated taxon-rich phylogenetic analyses that have resolved organismal relationships among many land plant groups. However, the relationships among major fern lineages, especially the placement of Equisetales, remain enigmatic. RESULTS: In order to understand the evolution of plastid genomes and to establish phylogenetic relationships among ferns, we sequenced the plastid genomes from three early diverging species: Equisetum hyemale (Equisetales), Ophioglossum californicum (Ophioglossales), and Psilotum nudum (Psilotales). A comparison of fern plastid genomes showed that some lineages have retained inverted repeat (IR) boundaries originating from the common ancestor of land plants, while other lineages have experienced multiple IR changes including expansions and inversions. Genome content has remained stable throughout ferns, except for a few lineage-specific losses of genes and introns. Notably, the losses of the rps16 gene and the rps12i346 intron are shared among Psilotales, Ophioglossales, and Equisetales, while the gain of a mitochondrial atp1 intron is shared between Marattiales and Polypodiopsida. These genomic structural changes support the placement of Equisetales as sister to Ophioglossales + Psilotales and Marattiales as sister to Polypodiopsida. This result is augmented by some molecular phylogenetic analyses that recover the same relationships, whereas others suggest a relationship between Equisetales and Polypodiopsida. CONCLUSIONS: Although molecular analyses were inconsistent with respect to the position of Marattiales and Equisetales, several genomic structural changes have for the first time provided a clear placement of these lineages within the ferns. These results further demonstrate the power of using rare genomic structural changes in cases where molecular data fail to provide strong phylogenetic resolution. BioMed Central 2013-01-11 /pmc/articles/PMC3553075/ /pubmed/23311954 http://dx.doi.org/10.1186/1471-2148-13-8 Text en Copyright ©2013 Grewe et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Grewe, Felix
Guo, Wenhu
Gubbels, Emily A
Hansen, A Katie
Mower, Jeffrey P
Complete plastid genomes from Ophioglossum californicum, Psilotum nudum, and Equisetum hyemale reveal an ancestral land plant genome structure and resolve the position of Equisetales among monilophytes
title Complete plastid genomes from Ophioglossum californicum, Psilotum nudum, and Equisetum hyemale reveal an ancestral land plant genome structure and resolve the position of Equisetales among monilophytes
title_full Complete plastid genomes from Ophioglossum californicum, Psilotum nudum, and Equisetum hyemale reveal an ancestral land plant genome structure and resolve the position of Equisetales among monilophytes
title_fullStr Complete plastid genomes from Ophioglossum californicum, Psilotum nudum, and Equisetum hyemale reveal an ancestral land plant genome structure and resolve the position of Equisetales among monilophytes
title_full_unstemmed Complete plastid genomes from Ophioglossum californicum, Psilotum nudum, and Equisetum hyemale reveal an ancestral land plant genome structure and resolve the position of Equisetales among monilophytes
title_short Complete plastid genomes from Ophioglossum californicum, Psilotum nudum, and Equisetum hyemale reveal an ancestral land plant genome structure and resolve the position of Equisetales among monilophytes
title_sort complete plastid genomes from ophioglossum californicum, psilotum nudum, and equisetum hyemale reveal an ancestral land plant genome structure and resolve the position of equisetales among monilophytes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3553075/
https://www.ncbi.nlm.nih.gov/pubmed/23311954
http://dx.doi.org/10.1186/1471-2148-13-8
work_keys_str_mv AT grewefelix completeplastidgenomesfromophioglossumcalifornicumpsilotumnudumandequisetumhyemalerevealanancestrallandplantgenomestructureandresolvethepositionofequisetalesamongmonilophytes
AT guowenhu completeplastidgenomesfromophioglossumcalifornicumpsilotumnudumandequisetumhyemalerevealanancestrallandplantgenomestructureandresolvethepositionofequisetalesamongmonilophytes
AT gubbelsemilya completeplastidgenomesfromophioglossumcalifornicumpsilotumnudumandequisetumhyemalerevealanancestrallandplantgenomestructureandresolvethepositionofequisetalesamongmonilophytes
AT hansenakatie completeplastidgenomesfromophioglossumcalifornicumpsilotumnudumandequisetumhyemalerevealanancestrallandplantgenomestructureandresolvethepositionofequisetalesamongmonilophytes
AT mowerjeffreyp completeplastidgenomesfromophioglossumcalifornicumpsilotumnudumandequisetumhyemalerevealanancestrallandplantgenomestructureandresolvethepositionofequisetalesamongmonilophytes