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Challenging the Importance of Plastid Genome Structure Conservation: New Insights From Euglenophytes
Plastids, similar to mitochondria, are organelles of endosymbiotic origin, which retained their vestigial genomes (ptDNA). Their unique architecture, commonly referred to as the quadripartite (four-part) structure, is considered to be strictly conserved; however, the bulk of our knowledge on their v...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9728796/ https://www.ncbi.nlm.nih.gov/pubmed/36403966 http://dx.doi.org/10.1093/molbev/msac255 |
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author | Maciszewski, Kacper Fells, Alicja Karnkowska, Anna |
author_facet | Maciszewski, Kacper Fells, Alicja Karnkowska, Anna |
author_sort | Maciszewski, Kacper |
collection | PubMed |
description | Plastids, similar to mitochondria, are organelles of endosymbiotic origin, which retained their vestigial genomes (ptDNA). Their unique architecture, commonly referred to as the quadripartite (four-part) structure, is considered to be strictly conserved; however, the bulk of our knowledge on their variability and evolutionary transformations comes from studies of the primary plastids of green algae and land plants. To broaden our perspective, we obtained seven new ptDNA sequences from freshwater species of photosynthetic euglenids—a group that obtained secondary plastids, known to have dynamically evolving genome structure, via endosymbiosis with a green alga. Our analyses have demonstrated that the evolutionary history of euglenid plastid genome structure is exceptionally convoluted, with a patchy distribution of inverted ribosomal operon (rDNA) repeats, as well as several independent acquisitions of tandemly repeated rDNA copies. Moreover, we have shown that inverted repeats in euglenid ptDNA do not share their genome-stabilizing property documented in chlorophytes. We hypothesize that the degeneration of the quadripartite structure of euglenid plastid genomes is connected to the group II intron expansion. These findings challenge the current global paradigms of plastid genome architecture evolution and underscore the often-underestimated divergence between the functionality of shared traits in primary and complex plastid organelles. |
format | Online Article Text |
id | pubmed-9728796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-97287962022-12-08 Challenging the Importance of Plastid Genome Structure Conservation: New Insights From Euglenophytes Maciszewski, Kacper Fells, Alicja Karnkowska, Anna Mol Biol Evol Discoveries Plastids, similar to mitochondria, are organelles of endosymbiotic origin, which retained their vestigial genomes (ptDNA). Their unique architecture, commonly referred to as the quadripartite (four-part) structure, is considered to be strictly conserved; however, the bulk of our knowledge on their variability and evolutionary transformations comes from studies of the primary plastids of green algae and land plants. To broaden our perspective, we obtained seven new ptDNA sequences from freshwater species of photosynthetic euglenids—a group that obtained secondary plastids, known to have dynamically evolving genome structure, via endosymbiosis with a green alga. Our analyses have demonstrated that the evolutionary history of euglenid plastid genome structure is exceptionally convoluted, with a patchy distribution of inverted ribosomal operon (rDNA) repeats, as well as several independent acquisitions of tandemly repeated rDNA copies. Moreover, we have shown that inverted repeats in euglenid ptDNA do not share their genome-stabilizing property documented in chlorophytes. We hypothesize that the degeneration of the quadripartite structure of euglenid plastid genomes is connected to the group II intron expansion. These findings challenge the current global paradigms of plastid genome architecture evolution and underscore the often-underestimated divergence between the functionality of shared traits in primary and complex plastid organelles. Oxford University Press 2022-11-21 /pmc/articles/PMC9728796/ /pubmed/36403966 http://dx.doi.org/10.1093/molbev/msac255 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 | Discoveries Maciszewski, Kacper Fells, Alicja Karnkowska, Anna Challenging the Importance of Plastid Genome Structure Conservation: New Insights From Euglenophytes |
title | Challenging the Importance of Plastid Genome Structure Conservation: New Insights From Euglenophytes |
title_full | Challenging the Importance of Plastid Genome Structure Conservation: New Insights From Euglenophytes |
title_fullStr | Challenging the Importance of Plastid Genome Structure Conservation: New Insights From Euglenophytes |
title_full_unstemmed | Challenging the Importance of Plastid Genome Structure Conservation: New Insights From Euglenophytes |
title_short | Challenging the Importance of Plastid Genome Structure Conservation: New Insights From Euglenophytes |
title_sort | challenging the importance of plastid genome structure conservation: new insights from euglenophytes |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9728796/ https://www.ncbi.nlm.nih.gov/pubmed/36403966 http://dx.doi.org/10.1093/molbev/msac255 |
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