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Differential timing of gene expression and recruitment in independent origins of CAM in the Agavoideae (Asparagaceae)
Crassulacean acid metabolism (CAM) photosynthesis has evolved repeatedly across the plant tree of life, however our understanding of the genetic convergence across independent origins remains hampered by the lack of comparative studies. Here, we explore gene expression profiles in eight species from...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796715/ https://www.ncbi.nlm.nih.gov/pubmed/35596719 http://dx.doi.org/10.1111/nph.18267 |
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author | Heyduk, Karolina McAssey, Edward V. Leebens‐Mack, Jim |
author_facet | Heyduk, Karolina McAssey, Edward V. Leebens‐Mack, Jim |
author_sort | Heyduk, Karolina |
collection | PubMed |
description | Crassulacean acid metabolism (CAM) photosynthesis has evolved repeatedly across the plant tree of life, however our understanding of the genetic convergence across independent origins remains hampered by the lack of comparative studies. Here, we explore gene expression profiles in eight species from the Agavoideae (Asparagaceae) encompassing three independent origins of CAM. Using comparative physiology and transcriptomics, we examined the variable modes of CAM in this subfamily and the changes in gene expression across time of day and between well watered and drought‐stressed treatments. We further assessed gene expression and the molecular evolution of genes encoding phosphoenolpyruvate carboxylase (PPC), an enzyme required for primary carbon fixation in CAM. Most time‐of‐day expression profiles are largely conserved across all eight species and suggest that large perturbations to the central clock are not required for CAM evolution. By contrast, transcriptional response to drought is highly lineage specific. Yucca and Beschorneria have CAM‐like expression of PPC2, a copy of PPC that has never been shown to be recruited for CAM in angiosperms. Together the physiological and transcriptomic comparison of closely related C(3) and CAM species reveals similar gene expression profiles, with the notable exception of differential recruitment of carboxylase enzymes for CAM function. |
format | Online Article Text |
id | pubmed-9796715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97967152023-01-04 Differential timing of gene expression and recruitment in independent origins of CAM in the Agavoideae (Asparagaceae) Heyduk, Karolina McAssey, Edward V. Leebens‐Mack, Jim New Phytol Research Crassulacean acid metabolism (CAM) photosynthesis has evolved repeatedly across the plant tree of life, however our understanding of the genetic convergence across independent origins remains hampered by the lack of comparative studies. Here, we explore gene expression profiles in eight species from the Agavoideae (Asparagaceae) encompassing three independent origins of CAM. Using comparative physiology and transcriptomics, we examined the variable modes of CAM in this subfamily and the changes in gene expression across time of day and between well watered and drought‐stressed treatments. We further assessed gene expression and the molecular evolution of genes encoding phosphoenolpyruvate carboxylase (PPC), an enzyme required for primary carbon fixation in CAM. Most time‐of‐day expression profiles are largely conserved across all eight species and suggest that large perturbations to the central clock are not required for CAM evolution. By contrast, transcriptional response to drought is highly lineage specific. Yucca and Beschorneria have CAM‐like expression of PPC2, a copy of PPC that has never been shown to be recruited for CAM in angiosperms. Together the physiological and transcriptomic comparison of closely related C(3) and CAM species reveals similar gene expression profiles, with the notable exception of differential recruitment of carboxylase enzymes for CAM function. John Wiley and Sons Inc. 2022-06-14 2022-09 /pmc/articles/PMC9796715/ /pubmed/35596719 http://dx.doi.org/10.1111/nph.18267 Text en © 2022 The Authors. New Phytologist © 2022 New Phytologist Foundation. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Heyduk, Karolina McAssey, Edward V. Leebens‐Mack, Jim Differential timing of gene expression and recruitment in independent origins of CAM in the Agavoideae (Asparagaceae) |
title | Differential timing of gene expression and recruitment in independent origins of CAM in the Agavoideae (Asparagaceae) |
title_full | Differential timing of gene expression and recruitment in independent origins of CAM in the Agavoideae (Asparagaceae) |
title_fullStr | Differential timing of gene expression and recruitment in independent origins of CAM in the Agavoideae (Asparagaceae) |
title_full_unstemmed | Differential timing of gene expression and recruitment in independent origins of CAM in the Agavoideae (Asparagaceae) |
title_short | Differential timing of gene expression and recruitment in independent origins of CAM in the Agavoideae (Asparagaceae) |
title_sort | differential timing of gene expression and recruitment in independent origins of cam in the agavoideae (asparagaceae) |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796715/ https://www.ncbi.nlm.nih.gov/pubmed/35596719 http://dx.doi.org/10.1111/nph.18267 |
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