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Plant organ evolution revealed by phylotranscriptomics in Arabidopsis thaliana
The evolution of phenotypes occurs through changes both in protein sequence and gene expression levels. Though much of plant morphological evolution can be explained by changes in gene expression, examining its evolution has challenges. To gain a new perspective on organ evolution in plants, we appl...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548721/ https://www.ncbi.nlm.nih.gov/pubmed/28790409 http://dx.doi.org/10.1038/s41598-017-07866-6 |
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author | Lei, Li Steffen, Joshua G. Osborne, Edward J. Toomajian, Christopher |
author_facet | Lei, Li Steffen, Joshua G. Osborne, Edward J. Toomajian, Christopher |
author_sort | Lei, Li |
collection | PubMed |
description | The evolution of phenotypes occurs through changes both in protein sequence and gene expression levels. Though much of plant morphological evolution can be explained by changes in gene expression, examining its evolution has challenges. To gain a new perspective on organ evolution in plants, we applied a phylotranscriptomics approach. We combined a phylostratigraphic approach with gene expression based on the strand-specific RNA-seq data from seedling, floral bud, and root of 19 Arabidopsis thaliana accessions to examine the age and sequence divergence of transcriptomes from these organs and how they adapted over time. Our results indicate that, among the sense and antisense transcriptomes of these organs, the sense transcriptomes of seedlings are the evolutionarily oldest across all accessions and are the most conserved in amino acid sequence for most accessions. In contrast, among the sense transcriptomes from these same organs, those from floral bud are evolutionarily youngest and least conserved in sequence for most accessions. Different organs have adaptive peaks at different stages in their evolutionary history; however, all three show a common adaptive signal from the Magnoliophyta to Brassicale stage. Our research highlights how phylotranscriptomic analyses can be used to trace organ evolution in the deep history of plant species. |
format | Online Article Text |
id | pubmed-5548721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55487212017-08-09 Plant organ evolution revealed by phylotranscriptomics in Arabidopsis thaliana Lei, Li Steffen, Joshua G. Osborne, Edward J. Toomajian, Christopher Sci Rep Article The evolution of phenotypes occurs through changes both in protein sequence and gene expression levels. Though much of plant morphological evolution can be explained by changes in gene expression, examining its evolution has challenges. To gain a new perspective on organ evolution in plants, we applied a phylotranscriptomics approach. We combined a phylostratigraphic approach with gene expression based on the strand-specific RNA-seq data from seedling, floral bud, and root of 19 Arabidopsis thaliana accessions to examine the age and sequence divergence of transcriptomes from these organs and how they adapted over time. Our results indicate that, among the sense and antisense transcriptomes of these organs, the sense transcriptomes of seedlings are the evolutionarily oldest across all accessions and are the most conserved in amino acid sequence for most accessions. In contrast, among the sense transcriptomes from these same organs, those from floral bud are evolutionarily youngest and least conserved in sequence for most accessions. Different organs have adaptive peaks at different stages in their evolutionary history; however, all three show a common adaptive signal from the Magnoliophyta to Brassicale stage. Our research highlights how phylotranscriptomic analyses can be used to trace organ evolution in the deep history of plant species. Nature Publishing Group UK 2017-08-08 /pmc/articles/PMC5548721/ /pubmed/28790409 http://dx.doi.org/10.1038/s41598-017-07866-6 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lei, Li Steffen, Joshua G. Osborne, Edward J. Toomajian, Christopher Plant organ evolution revealed by phylotranscriptomics in Arabidopsis thaliana |
title | Plant organ evolution revealed by phylotranscriptomics in Arabidopsis thaliana |
title_full | Plant organ evolution revealed by phylotranscriptomics in Arabidopsis thaliana |
title_fullStr | Plant organ evolution revealed by phylotranscriptomics in Arabidopsis thaliana |
title_full_unstemmed | Plant organ evolution revealed by phylotranscriptomics in Arabidopsis thaliana |
title_short | Plant organ evolution revealed by phylotranscriptomics in Arabidopsis thaliana |
title_sort | plant organ evolution revealed by phylotranscriptomics in arabidopsis thaliana |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548721/ https://www.ncbi.nlm.nih.gov/pubmed/28790409 http://dx.doi.org/10.1038/s41598-017-07866-6 |
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