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...

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Published in:Global Change Biology
Main Authors: Kang, Jingliang, Nagelkerken, Ivan, Rummer, Jodie L., Rodolfo-Metalpa, Riccardo, Munday, Philip L., Ravasi, Timothy, Schunter, Celia
Format: Article in Journal/Newspaper
Language:unknown
Published: Blackwell Publishing 2022
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Online Access:https://researchonline.jcu.edu.au/74524/1/74524.pdf
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spelling ftjamescook:oai:researchonline.jcu.edu.au:74524 2024-02-11T10:07:26+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 2022 application/pdf https://researchonline.jcu.edu.au/74524/1/74524.pdf unknown Blackwell Publishing https://doi.org/10.1111/gcb.16119 https://researchonline.jcu.edu.au/74524/ https://researchonline.jcu.edu.au/74524/1/74524.pdf Kang, Jingliang, Nagelkerken, Ivan, Rummer, Jodie L., Rodolfo-Metalpa, Riccardo, Munday, Philip L., Ravasi, Timothy, and Schunter, Celia (2022) Rapid evolution fuels transcriptional plasticity to ocean acidification. Global Change Biology, 28 (9). pp. 3007-3022. open Article PeerReviewed 2022 ftjamescook https://doi.org/10.1111/gcb.16119 2024-01-15T23:53:25Z 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. Article in Journal/Newspaper Ocean acidification James Cook University, Australia: ResearchOnline@JCU Global Change Biology 28 9 3007 3022
institution Open Polar
collection James Cook University, Australia: ResearchOnline@JCU
op_collection_id ftjamescook
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.
format Article in Journal/Newspaper
author Kang, Jingliang
Nagelkerken, Ivan
Rummer, Jodie L.
Rodolfo-Metalpa, Riccardo
Munday, Philip L.
Ravasi, Timothy
Schunter, Celia
spellingShingle 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
author_facet Kang, Jingliang
Nagelkerken, Ivan
Rummer, Jodie L.
Rodolfo-Metalpa, Riccardo
Munday, Philip L.
Ravasi, Timothy
Schunter, Celia
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 Blackwell Publishing
publishDate 2022
url https://researchonline.jcu.edu.au/74524/1/74524.pdf
genre Ocean acidification
genre_facet Ocean acidification
op_relation https://doi.org/10.1111/gcb.16119
https://researchonline.jcu.edu.au/74524/
https://researchonline.jcu.edu.au/74524/1/74524.pdf
Kang, Jingliang, Nagelkerken, Ivan, Rummer, Jodie L., Rodolfo-Metalpa, Riccardo, Munday, Philip L., Ravasi, Timothy, and Schunter, Celia (2022) Rapid evolution fuels transcriptional plasticity to ocean acidification. Global Change Biology, 28 (9). pp. 3007-3022.
op_rights open
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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