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Article: Rapid evolution fuels transcriptional plasticity to ocean acidification

TitleRapid evolution fuels transcriptional plasticity to ocean acidification
Authors
Keywordscircadian rhythm
climate change
elevated pCO2
intracellular pH
neuromolecular response
transcriptome
Issue Date3-Mar-2022
PublisherWiley
Citation
Global Change Biology, 2022, v. 28, n. 9, p. 3007-3022 How to Cite?
Abstract

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 CO2 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 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.


Persistent Identifierhttp://hdl.handle.net/10722/331378
ISSN
2021 Impact Factor: 13.211
2020 SCImago Journal Rankings: 4.146

 

DC FieldValueLanguage
dc.contributor.authorKang, JL-
dc.contributor.authorNagelkerken, I-
dc.contributor.authorRummer, JL-
dc.contributor.authorRodolfo-Metalpa, R-
dc.contributor.authorMunday, PL-
dc.contributor.authorRavasi, T-
dc.contributor.authorSchunter, C-
dc.date.accessioned2023-09-21T06:55:12Z-
dc.date.available2023-09-21T06:55:12Z-
dc.date.issued2022-03-03-
dc.identifier.citationGlobal Change Biology, 2022, v. 28, n. 9, p. 3007-3022-
dc.identifier.issn1354-1013-
dc.identifier.urihttp://hdl.handle.net/10722/331378-
dc.description.abstract<p>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 CO2 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 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.<br></p>-
dc.languageeng-
dc.publisherWiley-
dc.relation.ispartofGlobal Change Biology-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectcircadian rhythm-
dc.subjectclimate change-
dc.subjectelevated pCO2-
dc.subjectintracellular pH-
dc.subjectneuromolecular response-
dc.subjecttranscriptome-
dc.titleRapid evolution fuels transcriptional plasticity to ocean acidification-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1111/gcb.16119-
dc.identifier.scopuseid_2-s2.0-85125518266-
dc.identifier.volume28-
dc.identifier.issue9-
dc.identifier.spage3007-
dc.identifier.epage3022-
dc.identifier.eissn1365-2486-
dc.identifier.issnl1354-1013-

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