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Parallel evolution of highly conserved plastid genome architecture in red seaweeds and seed plants

BACKGROUND: The red algae (Rhodophyta) diverged from the green algae and plants (Viridiplantae) over one billion years ago within the kingdom Archaeplastida. These photosynthetic lineages provide an ideal model to study plastid genome reduction in deep time. To this end, we assembled a large dataset...

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Autores principales: Lee, JunMo, Cho, Chung Hyun, Park, Seung In, Choi, Ji Won, Song, Hyun Suk, West, John A., Bhattacharya, Debashish, Yoon, Hwan Su
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5010701/
https://www.ncbi.nlm.nih.gov/pubmed/27589960
http://dx.doi.org/10.1186/s12915-016-0299-5
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author Lee, JunMo
Cho, Chung Hyun
Park, Seung In
Choi, Ji Won
Song, Hyun Suk
West, John A.
Bhattacharya, Debashish
Yoon, Hwan Su
author_facet Lee, JunMo
Cho, Chung Hyun
Park, Seung In
Choi, Ji Won
Song, Hyun Suk
West, John A.
Bhattacharya, Debashish
Yoon, Hwan Su
author_sort Lee, JunMo
collection PubMed
description BACKGROUND: The red algae (Rhodophyta) diverged from the green algae and plants (Viridiplantae) over one billion years ago within the kingdom Archaeplastida. These photosynthetic lineages provide an ideal model to study plastid genome reduction in deep time. To this end, we assembled a large dataset of the plastid genomes that were available, including 48 from the red algae (17 complete and three partial genomes produced for this analysis) to elucidate the evolutionary history of these organelles. RESULTS: We found extreme conservation of plastid genome architecture in the major lineages of the multicellular Florideophyceae red algae. Only three minor structural types were detected in this group, which are explained by recombination events of the duplicated rDNA operons. A similar high level of structural conservation (although with different gene content) was found in seed plants. Three major plastid genome architectures were identified in representatives of 46 orders of angiosperms and three orders of gymnosperms. CONCLUSIONS: Our results provide a comprehensive account of plastid gene loss and rearrangement events involving genome architecture within Archaeplastida and lead to one over-arching conclusion: from an ancestral pool of highly rearranged plastid genomes in red and green algae, the aquatic (Florideophyceae) and terrestrial (seed plants) multicellular lineages display high conservation in plastid genome architecture. This phenomenon correlates with, and could be explained by, the independent and widely divergent (separated by >400 million years) origins of complex sexual cycles and reproductive structures that led to the rapid diversification of these lineages. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-016-0299-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-50107012016-09-04 Parallel evolution of highly conserved plastid genome architecture in red seaweeds and seed plants Lee, JunMo Cho, Chung Hyun Park, Seung In Choi, Ji Won Song, Hyun Suk West, John A. Bhattacharya, Debashish Yoon, Hwan Su BMC Biol Research Article BACKGROUND: The red algae (Rhodophyta) diverged from the green algae and plants (Viridiplantae) over one billion years ago within the kingdom Archaeplastida. These photosynthetic lineages provide an ideal model to study plastid genome reduction in deep time. To this end, we assembled a large dataset of the plastid genomes that were available, including 48 from the red algae (17 complete and three partial genomes produced for this analysis) to elucidate the evolutionary history of these organelles. RESULTS: We found extreme conservation of plastid genome architecture in the major lineages of the multicellular Florideophyceae red algae. Only three minor structural types were detected in this group, which are explained by recombination events of the duplicated rDNA operons. A similar high level of structural conservation (although with different gene content) was found in seed plants. Three major plastid genome architectures were identified in representatives of 46 orders of angiosperms and three orders of gymnosperms. CONCLUSIONS: Our results provide a comprehensive account of plastid gene loss and rearrangement events involving genome architecture within Archaeplastida and lead to one over-arching conclusion: from an ancestral pool of highly rearranged plastid genomes in red and green algae, the aquatic (Florideophyceae) and terrestrial (seed plants) multicellular lineages display high conservation in plastid genome architecture. This phenomenon correlates with, and could be explained by, the independent and widely divergent (separated by >400 million years) origins of complex sexual cycles and reproductive structures that led to the rapid diversification of these lineages. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-016-0299-5) contains supplementary material, which is available to authorized users. BioMed Central 2016-09-02 /pmc/articles/PMC5010701/ /pubmed/27589960 http://dx.doi.org/10.1186/s12915-016-0299-5 Text en © Yoon et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Lee, JunMo
Cho, Chung Hyun
Park, Seung In
Choi, Ji Won
Song, Hyun Suk
West, John A.
Bhattacharya, Debashish
Yoon, Hwan Su
Parallel evolution of highly conserved plastid genome architecture in red seaweeds and seed plants
title Parallel evolution of highly conserved plastid genome architecture in red seaweeds and seed plants
title_full Parallel evolution of highly conserved plastid genome architecture in red seaweeds and seed plants
title_fullStr Parallel evolution of highly conserved plastid genome architecture in red seaweeds and seed plants
title_full_unstemmed Parallel evolution of highly conserved plastid genome architecture in red seaweeds and seed plants
title_short Parallel evolution of highly conserved plastid genome architecture in red seaweeds and seed plants
title_sort parallel evolution of highly conserved plastid genome architecture in red seaweeds and seed plants
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5010701/
https://www.ncbi.nlm.nih.gov/pubmed/27589960
http://dx.doi.org/10.1186/s12915-016-0299-5
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