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 pCO2 in wild populations remains largely untested. We measured brain transcriptomes of six coral reef fish species at a natural volca...
Published in: | Global Change Biology |
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Online Access: | http://hdl.handle.net/10754/678172 https://doi.org/10.1111/gcb.16119 |
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ftkingabdullahun:oai:repository.kaust.edu.sa:10754/678172 2024-01-07T09:45:43+01:00 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 Marei Swire Institute of Marine Science, School of Biological Sciences, The University of Hong Kong, Hong Kong, Hong Kong SAR, China Southern Seas Ecology Laboratories, School of Biological Sciences & The Environment Institute, The University of Adelaide, Adelaide, South Australia, Australia Australian Research Council Centre of Excellence for Coral Reef Studies, James Cook University, Townsville, Australia College of Science and Engineering, James Cook University, Townsville, Queensland, Australia ENTROPIE – UMR 9220 (CNRS, IRD, UR, UNC, IFREMER), IRD Institut de Recherche pour le Développement, Nouméa cedex, New Caledonia Marine Climate Change Unit, Okinawa Institute of Science and Technology Graduate University, Onna-son, Japan State Key Laboratory of Marine Pollution, City University of Hong Kong, Hong Kong, Hong Kong SAR, China 2022-03-03 http://hdl.handle.net/10754/678172 https://doi.org/10.1111/gcb.16119 unknown Wiley https://onlinelibrary.wiley.com/doi/10.1111/gcb.16119 Kang, J., Nagelkerken, I., Rummer, J. L., Rodolfo-Metalpa, R., Munday, P. L., Ravasi, T., & Schunter, C. (2022). Rapid evolution fuels transcriptional plasticity to ocean acidification. Global Change Biology. Portico. https://doi.org/10.1111/gcb.16119 doi:10.1111/gcb.16119 2-s2.0-85125518266 1365-2486 1354-1013 9 Global Change Biology 3007-3022 http://hdl.handle.net/10754/678172 28 Article 2022 ftkingabdullahun https://doi.org/10.1111/gcb.16119 2023-12-09T20:17:55Z Ocean acidification (OA) is postulated to affect the physiology, behavior, and life-history of marine species, but potential for acclimation or adaptation to elevated pCO2 in wild populations remains largely untested. We measured brain transcriptomes of six coral reef fish species at a natural volcanic CO2 seep and an adjacent control reef in Papua New Guinea. We show that elevated pCO2 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 CO2 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 CO2, 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. King Abdullah University of Science and Technology, Grant/Award Number: OSR-2015-CRG4-2541; The Okinawa Institute of Science and Technology Graduate University; the French National Research Agency, Grant/Award Number: ANR15CE02-0006- 01 and ANR-17- ERC2- 0009; the University of Hong Kong start- up grant; the Australian Research Council (ARC) and ARC Centre of Excellence for Coral Reef Studies, Grant/Award Number: FT120100183 We are grateful to the local communities for access to their reef and to the National Research Institute and the Milne Bay Provincial Research Committee for approval to conduct research at this site. Thanks to Prof. Ralph Mana (School of Natural and Physical Sciences, University of Papua New Guinea) for his invaluable support to obtain PNG permits. We are grateful to the population ... Article in Journal/Newspaper Ocean acidification King Abdullah University of Science and Technology: KAUST Repository Milne Bay ENVELOPE(-99.713,-99.713,58.901,58.901) Global Change Biology 28 9 3007 3022 |
institution |
Open Polar |
collection |
King Abdullah University of Science and Technology: KAUST Repository |
op_collection_id |
ftkingabdullahun |
language |
unknown |
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 pCO2 in wild populations remains largely untested. We measured brain transcriptomes of six coral reef fish species at a natural volcanic CO2 seep and an adjacent control reef in Papua New Guinea. We show that elevated pCO2 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 CO2 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 CO2, 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. King Abdullah University of Science and Technology, Grant/Award Number: OSR-2015-CRG4-2541; The Okinawa Institute of Science and Technology Graduate University; the French National Research Agency, Grant/Award Number: ANR15CE02-0006- 01 and ANR-17- ERC2- 0009; the University of Hong Kong start- up grant; the Australian Research Council (ARC) and ARC Centre of Excellence for Coral Reef Studies, Grant/Award Number: FT120100183 We are grateful to the local communities for access to their reef and to the National Research Institute and the Milne Bay Provincial Research Committee for approval to conduct research at this site. Thanks to Prof. Ralph Mana (School of Natural and Physical Sciences, University of Papua New Guinea) for his invaluable support to obtain PNG permits. We are grateful to the population ... |
author2 |
Swire Institute of Marine Science, School of Biological Sciences, The University of Hong Kong, Hong Kong, Hong Kong SAR, China Southern Seas Ecology Laboratories, School of Biological Sciences & The Environment Institute, The University of Adelaide, Adelaide, South Australia, Australia Australian Research Council Centre of Excellence for Coral Reef Studies, James Cook University, Townsville, Australia College of Science and Engineering, James Cook University, Townsville, Queensland, Australia ENTROPIE – UMR 9220 (CNRS, IRD, UR, UNC, IFREMER), IRD Institut de Recherche pour le Développement, Nouméa cedex, New Caledonia Marine Climate Change Unit, Okinawa Institute of Science and Technology Graduate University, Onna-son, Japan State Key Laboratory of Marine Pollution, City University of Hong Kong, Hong Kong, Hong Kong SAR, China |
format |
Article in Journal/Newspaper |
author |
Kang, Jingliang Nagelkerken, Ivan Rummer, Jodie L. Rodolfo-Metalpa, Riccardo Munday, Philip L. Ravasi, Timothy Schunter, Celia Marei |
spellingShingle |
Kang, Jingliang Nagelkerken, Ivan Rummer, Jodie L. Rodolfo-Metalpa, Riccardo Munday, Philip L. Ravasi, Timothy Schunter, Celia Marei Rapid evolution fuels transcriptional plasticity to ocean acidification |
author_facet |
Kang, Jingliang Nagelkerken, Ivan Rummer, Jodie L. Rodolfo-Metalpa, Riccardo Munday, Philip L. Ravasi, Timothy Schunter, Celia Marei |
author_sort |
Kang, Jingliang |
title |
Rapid evolution fuels transcriptional plasticity to ocean acidification |
title_short |
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_sort |
rapid evolution fuels transcriptional plasticity to ocean acidification |
publisher |
Wiley |
publishDate |
2022 |
url |
http://hdl.handle.net/10754/678172 https://doi.org/10.1111/gcb.16119 |
long_lat |
ENVELOPE(-99.713,-99.713,58.901,58.901) |
geographic |
Milne Bay |
geographic_facet |
Milne Bay |
genre |
Ocean acidification |
genre_facet |
Ocean acidification |
op_relation |
https://onlinelibrary.wiley.com/doi/10.1111/gcb.16119 Kang, J., Nagelkerken, I., Rummer, J. L., Rodolfo-Metalpa, R., Munday, P. L., Ravasi, T., & Schunter, C. (2022). Rapid evolution fuels transcriptional plasticity to ocean acidification. Global Change Biology. Portico. https://doi.org/10.1111/gcb.16119 doi:10.1111/gcb.16119 2-s2.0-85125518266 1365-2486 1354-1013 9 Global Change Biology 3007-3022 http://hdl.handle.net/10754/678172 28 |
op_doi |
https://doi.org/10.1111/gcb.16119 |
container_title |
Global Change Biology |
container_volume |
28 |
container_issue |
9 |
container_start_page |
3007 |
op_container_end_page |
3022 |
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1787427305067380736 |