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Selection on oxidative phosphorylation and ribosomal structure as a multigenerational response to ocean acidification in the common copepod Pseudocalanus acuspes
Ocean acidification is expected to have dramatic impacts on oceanic ecosystems, yet surprisingly few studies currently examine long‐term adaptive and plastic responses of marine invertebrates to pCO (2) stress. Here, we exposed populations of the common copepod Pseudocalanus acuspes to three pCO (2)...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039324/ https://www.ncbi.nlm.nih.gov/pubmed/27695519 http://dx.doi.org/10.1111/eva.12335 |
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author | De Wit, Pierre Dupont, Sam Thor, Peter |
author_facet | De Wit, Pierre Dupont, Sam Thor, Peter |
author_sort | De Wit, Pierre |
collection | PubMed |
description | Ocean acidification is expected to have dramatic impacts on oceanic ecosystems, yet surprisingly few studies currently examine long‐term adaptive and plastic responses of marine invertebrates to pCO (2) stress. Here, we exposed populations of the common copepod Pseudocalanus acuspes to three pCO (2) regimes (400, 900, and 1550 μatm) for two generations, after which we conducted a reciprocal transplant experiment. A de novo transcriptome was assembled, annotated, and gene expression data revealed that genes involved in RNA transcription were strongly down‐regulated in populations with long‐term exposure to a high pCO (2) environment, even after transplantation back to control levels. In addition, 747 000 SNPs were identified, out of which 1513 showed consistent changes in nucleotide frequency between replicates of control and high pCO (2) populations. Functions involving RNA transcription and ribosomal function, as well as ion transport and oxidative phosphorylation, were highly overrepresented. We thus conclude that pCO (2) stress appears to impose selection in copepods on RNA synthesis and translation, possibly modulated by helicase expression. Using a physiological hypothesis‐testing strategy to mine gene expression data, we herein increase the power to detect cellular targets of ocean acidification. This novel approach seems promising for future studies of effects of environmental changes in ecologically important nonmodel organisms. |
format | Online Article Text |
id | pubmed-5039324 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50393242016-09-30 Selection on oxidative phosphorylation and ribosomal structure as a multigenerational response to ocean acidification in the common copepod Pseudocalanus acuspes De Wit, Pierre Dupont, Sam Thor, Peter Evol Appl Original Articles Ocean acidification is expected to have dramatic impacts on oceanic ecosystems, yet surprisingly few studies currently examine long‐term adaptive and plastic responses of marine invertebrates to pCO (2) stress. Here, we exposed populations of the common copepod Pseudocalanus acuspes to three pCO (2) regimes (400, 900, and 1550 μatm) for two generations, after which we conducted a reciprocal transplant experiment. A de novo transcriptome was assembled, annotated, and gene expression data revealed that genes involved in RNA transcription were strongly down‐regulated in populations with long‐term exposure to a high pCO (2) environment, even after transplantation back to control levels. In addition, 747 000 SNPs were identified, out of which 1513 showed consistent changes in nucleotide frequency between replicates of control and high pCO (2) populations. Functions involving RNA transcription and ribosomal function, as well as ion transport and oxidative phosphorylation, were highly overrepresented. We thus conclude that pCO (2) stress appears to impose selection in copepods on RNA synthesis and translation, possibly modulated by helicase expression. Using a physiological hypothesis‐testing strategy to mine gene expression data, we herein increase the power to detect cellular targets of ocean acidification. This novel approach seems promising for future studies of effects of environmental changes in ecologically important nonmodel organisms. John Wiley and Sons Inc. 2015-11-23 /pmc/articles/PMC5039324/ /pubmed/27695519 http://dx.doi.org/10.1111/eva.12335 Text en © 2015 The Authors. Evolutionary Applications published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles De Wit, Pierre Dupont, Sam Thor, Peter Selection on oxidative phosphorylation and ribosomal structure as a multigenerational response to ocean acidification in the common copepod Pseudocalanus acuspes |
title | Selection on oxidative phosphorylation and ribosomal structure as a multigenerational response to ocean acidification in the common copepod Pseudocalanus acuspes
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title_full | Selection on oxidative phosphorylation and ribosomal structure as a multigenerational response to ocean acidification in the common copepod Pseudocalanus acuspes
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title_fullStr | Selection on oxidative phosphorylation and ribosomal structure as a multigenerational response to ocean acidification in the common copepod Pseudocalanus acuspes
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title_full_unstemmed | Selection on oxidative phosphorylation and ribosomal structure as a multigenerational response to ocean acidification in the common copepod Pseudocalanus acuspes
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title_short | Selection on oxidative phosphorylation and ribosomal structure as a multigenerational response to ocean acidification in the common copepod Pseudocalanus acuspes
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title_sort | selection on oxidative phosphorylation and ribosomal structure as a multigenerational response to ocean acidification in the common copepod pseudocalanus acuspes |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039324/ https://www.ncbi.nlm.nih.gov/pubmed/27695519 http://dx.doi.org/10.1111/eva.12335 |
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