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Gene expression and epigenetic responses of the marine Cladoceran, Evadne nordmanni, and the copepod, Acartia clausi, to elevated CO(2)

Characterizing the capacity of marine organisms to adapt to climate change related drivers (e.g., pCO(2) and temperature), and the possible rate of this adaptation, is required to assess their resilience (or lack thereof) to these drivers. Several studies have hypothesized that epigenetic markers su...

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Autores principales: Aluru, Neelakanteswar, Fields, David M., Shema, Steven, Skiftesvik, Anne Berit, Browman, Howard I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8668794/
https://www.ncbi.nlm.nih.gov/pubmed/34938472
http://dx.doi.org/10.1002/ece3.8309
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author Aluru, Neelakanteswar
Fields, David M.
Shema, Steven
Skiftesvik, Anne Berit
Browman, Howard I.
author_facet Aluru, Neelakanteswar
Fields, David M.
Shema, Steven
Skiftesvik, Anne Berit
Browman, Howard I.
author_sort Aluru, Neelakanteswar
collection PubMed
description Characterizing the capacity of marine organisms to adapt to climate change related drivers (e.g., pCO(2) and temperature), and the possible rate of this adaptation, is required to assess their resilience (or lack thereof) to these drivers. Several studies have hypothesized that epigenetic markers such as DNA methylation, histone modifications and noncoding RNAs, act as drivers of adaptation in marine organisms, especially corals. However, this hypothesis has not been tested in zooplankton, a keystone organism in marine food webs. The objective of this study is to test the hypothesis that acute ocean acidification (OA) exposure alters DNA methylation in two zooplanktonic species—copepods (Acartia clausii) and cladocerans (Evadne nordmanii). We exposed these two species to near‐future OA conditions (400 and 900 ppm pCO(2)) for 24 h and assessed transcriptional and DNA methylation patterns using RNA sequencing and Reduced Representation Bisulfite Sequencing (RRBS). OA exposure caused differential expression of genes associated with energy metabolism, cytoskeletal and extracellular matrix functions, hypoxia and one‐carbon metabolism. Similarly, OA exposure also caused altered DNA methylation patterns in both species but the effect of these changes on gene expression and physiological effects remains to be determined. The results from this study form the basis for studies investigating the potential role of epigenetic mechanisms in OA induced phenotypic plasticity and/or adaptive responses in zooplanktonic organisms.
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spelling pubmed-86687942021-12-21 Gene expression and epigenetic responses of the marine Cladoceran, Evadne nordmanni, and the copepod, Acartia clausi, to elevated CO(2) Aluru, Neelakanteswar Fields, David M. Shema, Steven Skiftesvik, Anne Berit Browman, Howard I. Ecol Evol Research Articles Characterizing the capacity of marine organisms to adapt to climate change related drivers (e.g., pCO(2) and temperature), and the possible rate of this adaptation, is required to assess their resilience (or lack thereof) to these drivers. Several studies have hypothesized that epigenetic markers such as DNA methylation, histone modifications and noncoding RNAs, act as drivers of adaptation in marine organisms, especially corals. However, this hypothesis has not been tested in zooplankton, a keystone organism in marine food webs. The objective of this study is to test the hypothesis that acute ocean acidification (OA) exposure alters DNA methylation in two zooplanktonic species—copepods (Acartia clausii) and cladocerans (Evadne nordmanii). We exposed these two species to near‐future OA conditions (400 and 900 ppm pCO(2)) for 24 h and assessed transcriptional and DNA methylation patterns using RNA sequencing and Reduced Representation Bisulfite Sequencing (RRBS). OA exposure caused differential expression of genes associated with energy metabolism, cytoskeletal and extracellular matrix functions, hypoxia and one‐carbon metabolism. Similarly, OA exposure also caused altered DNA methylation patterns in both species but the effect of these changes on gene expression and physiological effects remains to be determined. The results from this study form the basis for studies investigating the potential role of epigenetic mechanisms in OA induced phenotypic plasticity and/or adaptive responses in zooplanktonic organisms. John Wiley and Sons Inc. 2021-11-23 /pmc/articles/PMC8668794/ /pubmed/34938472 http://dx.doi.org/10.1002/ece3.8309 Text en © 2021 The Authors. Ecology and Evolution 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
Aluru, Neelakanteswar
Fields, David M.
Shema, Steven
Skiftesvik, Anne Berit
Browman, Howard I.
Gene expression and epigenetic responses of the marine Cladoceran, Evadne nordmanni, and the copepod, Acartia clausi, to elevated CO(2)
title Gene expression and epigenetic responses of the marine Cladoceran, Evadne nordmanni, and the copepod, Acartia clausi, to elevated CO(2)
title_full Gene expression and epigenetic responses of the marine Cladoceran, Evadne nordmanni, and the copepod, Acartia clausi, to elevated CO(2)
title_fullStr Gene expression and epigenetic responses of the marine Cladoceran, Evadne nordmanni, and the copepod, Acartia clausi, to elevated CO(2)
title_full_unstemmed Gene expression and epigenetic responses of the marine Cladoceran, Evadne nordmanni, and the copepod, Acartia clausi, to elevated CO(2)
title_short Gene expression and epigenetic responses of the marine Cladoceran, Evadne nordmanni, and the copepod, Acartia clausi, to elevated CO(2)
title_sort gene expression and epigenetic responses of the marine cladoceran, evadne nordmanni, and the copepod, acartia clausi, to elevated co(2)
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8668794/
https://www.ncbi.nlm.nih.gov/pubmed/34938472
http://dx.doi.org/10.1002/ece3.8309
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