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Rapid evolution fuels transcriptional plasticity to ocean acidification
Ocean acidification (OA) is postulated to affect the physiology, behavior, and life‐history of marine species, but potential for acclimation or adaptation to elevated pCO(2) in wild populations remains largely untested. We measured brain transcriptomes of six coral reef fish species at a natural vol...
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/PMC9310587/ https://www.ncbi.nlm.nih.gov/pubmed/35238117 http://dx.doi.org/10.1111/gcb.16119 |
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author | Kang, Jingliang Nagelkerken, Ivan Rummer, Jodie L. Rodolfo‐Metalpa, Riccardo Munday, Philip L. Ravasi, Timothy Schunter, Celia |
author_facet | Kang, Jingliang Nagelkerken, Ivan Rummer, Jodie L. Rodolfo‐Metalpa, Riccardo Munday, Philip L. Ravasi, Timothy Schunter, Celia |
author_sort | Kang, Jingliang |
collection | PubMed |
description | Ocean acidification (OA) is postulated to affect the physiology, behavior, and life‐history of marine species, but potential for acclimation or adaptation to elevated pCO(2) in wild populations remains largely untested. We measured brain transcriptomes of six coral reef fish species at a natural volcanic CO(2) seep and an adjacent control reef in Papua New Guinea. We show that elevated pCO(2) induced common molecular responses related to circadian rhythm and immune system but different magnitudes of molecular response across the six species. Notably, elevated transcriptional plasticity was associated with core circadian genes affecting the regulation of intracellular pH and neural activity in Acanthochromis polyacanthus. Gene expression patterns were reversible in this species as evidenced upon reduction of CO(2) following a natural storm‐event. Compared with other species, Ac. polyacanthus has a more rapid evolutionary rate and more positively selected genes in key functions under the influence of elevated CO(2), thus fueling increased transcriptional plasticity. Our study reveals the basis to variable gene expression changes across species, with some species possessing evolved molecular toolkits to cope with future OA. |
format | Online Article Text |
id | pubmed-9310587 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93105872022-07-29 Rapid evolution fuels transcriptional plasticity to ocean acidification Kang, Jingliang Nagelkerken, Ivan Rummer, Jodie L. Rodolfo‐Metalpa, Riccardo Munday, Philip L. Ravasi, Timothy Schunter, Celia Glob Chang Biol Research Articles Ocean acidification (OA) is postulated to affect the physiology, behavior, and life‐history of marine species, but potential for acclimation or adaptation to elevated pCO(2) in wild populations remains largely untested. We measured brain transcriptomes of six coral reef fish species at a natural volcanic CO(2) seep and an adjacent control reef in Papua New Guinea. We show that elevated pCO(2) induced common molecular responses related to circadian rhythm and immune system but different magnitudes of molecular response across the six species. Notably, elevated transcriptional plasticity was associated with core circadian genes affecting the regulation of intracellular pH and neural activity in Acanthochromis polyacanthus. Gene expression patterns were reversible in this species as evidenced upon reduction of CO(2) following a natural storm‐event. Compared with other species, Ac. polyacanthus has a more rapid evolutionary rate and more positively selected genes in key functions under the influence of elevated CO(2), thus fueling increased transcriptional plasticity. Our study reveals the basis to variable gene expression changes across species, with some species possessing evolved molecular toolkits to cope with future OA. John Wiley and Sons Inc. 2022-03-03 2022-05 /pmc/articles/PMC9310587/ /pubmed/35238117 http://dx.doi.org/10.1111/gcb.16119 Text en © 2022 The Authors. Global Change Biology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Kang, Jingliang Nagelkerken, Ivan Rummer, Jodie L. Rodolfo‐Metalpa, Riccardo Munday, Philip L. Ravasi, Timothy Schunter, Celia Rapid evolution fuels transcriptional plasticity to ocean acidification |
title | Rapid evolution fuels transcriptional plasticity to ocean acidification |
title_full | Rapid evolution fuels transcriptional plasticity to ocean acidification |
title_fullStr | Rapid evolution fuels transcriptional plasticity to ocean acidification |
title_full_unstemmed | Rapid evolution fuels transcriptional plasticity to ocean acidification |
title_short | Rapid evolution fuels transcriptional plasticity to ocean acidification |
title_sort | rapid evolution fuels transcriptional plasticity to ocean acidification |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310587/ https://www.ncbi.nlm.nih.gov/pubmed/35238117 http://dx.doi.org/10.1111/gcb.16119 |
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