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Remodeling of the cycling transcriptome of the oyster Crassostrea gigas by the harmful algae Alexandrium minutum
As a marine organism, the oyster Crassostrea gigas inhabits a complex biotope governed by interactions between the moon and the sun cycles. We used next-generation sequencing to investigate temporal regulation of oysters under light/dark entrainment and the impact of harmful algal exposure. We found...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471176/ https://www.ncbi.nlm.nih.gov/pubmed/28615697 http://dx.doi.org/10.1038/s41598-017-03797-4 |
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author | Payton, Laura Perrigault, Mickael Hoede, Claire Massabuau, Jean-Charles Sow, Mohamedou Huvet, Arnaud Boullot, Floriane Fabioux, Caroline Hegaret, Hélène Tran, Damien |
author_facet | Payton, Laura Perrigault, Mickael Hoede, Claire Massabuau, Jean-Charles Sow, Mohamedou Huvet, Arnaud Boullot, Floriane Fabioux, Caroline Hegaret, Hélène Tran, Damien |
author_sort | Payton, Laura |
collection | PubMed |
description | As a marine organism, the oyster Crassostrea gigas inhabits a complex biotope governed by interactions between the moon and the sun cycles. We used next-generation sequencing to investigate temporal regulation of oysters under light/dark entrainment and the impact of harmful algal exposure. We found that ≈6% of the gills’ transcriptome exhibits circadian expression, characterized by a nocturnal and bimodal pattern. Surprisingly, a higher number of ultradian transcripts were also detected under solely circadian entrainment. The results showed that a bloom of Alexandrium minutum generated a remodeling of the bivalve’s temporal structure, characterized by a loss of oscillations, a genesis of de novo oscillating transcripts, and a switch in the period of oscillations. These findings provide unprecedented insights into the diurnal landscape of the oyster’s transcriptome and pleiotropic remodeling due to toxic algae exposure, revealing the intrinsic plasticity of the cycling transcriptome in oysters. |
format | Online Article Text |
id | pubmed-5471176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54711762017-06-19 Remodeling of the cycling transcriptome of the oyster Crassostrea gigas by the harmful algae Alexandrium minutum Payton, Laura Perrigault, Mickael Hoede, Claire Massabuau, Jean-Charles Sow, Mohamedou Huvet, Arnaud Boullot, Floriane Fabioux, Caroline Hegaret, Hélène Tran, Damien Sci Rep Article As a marine organism, the oyster Crassostrea gigas inhabits a complex biotope governed by interactions between the moon and the sun cycles. We used next-generation sequencing to investigate temporal regulation of oysters under light/dark entrainment and the impact of harmful algal exposure. We found that ≈6% of the gills’ transcriptome exhibits circadian expression, characterized by a nocturnal and bimodal pattern. Surprisingly, a higher number of ultradian transcripts were also detected under solely circadian entrainment. The results showed that a bloom of Alexandrium minutum generated a remodeling of the bivalve’s temporal structure, characterized by a loss of oscillations, a genesis of de novo oscillating transcripts, and a switch in the period of oscillations. These findings provide unprecedented insights into the diurnal landscape of the oyster’s transcriptome and pleiotropic remodeling due to toxic algae exposure, revealing the intrinsic plasticity of the cycling transcriptome in oysters. Nature Publishing Group UK 2017-06-14 /pmc/articles/PMC5471176/ /pubmed/28615697 http://dx.doi.org/10.1038/s41598-017-03797-4 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Payton, Laura Perrigault, Mickael Hoede, Claire Massabuau, Jean-Charles Sow, Mohamedou Huvet, Arnaud Boullot, Floriane Fabioux, Caroline Hegaret, Hélène Tran, Damien Remodeling of the cycling transcriptome of the oyster Crassostrea gigas by the harmful algae Alexandrium minutum |
title | Remodeling of the cycling transcriptome of the oyster Crassostrea gigas by the harmful algae Alexandrium minutum |
title_full | Remodeling of the cycling transcriptome of the oyster Crassostrea gigas by the harmful algae Alexandrium minutum |
title_fullStr | Remodeling of the cycling transcriptome of the oyster Crassostrea gigas by the harmful algae Alexandrium minutum |
title_full_unstemmed | Remodeling of the cycling transcriptome of the oyster Crassostrea gigas by the harmful algae Alexandrium minutum |
title_short | Remodeling of the cycling transcriptome of the oyster Crassostrea gigas by the harmful algae Alexandrium minutum |
title_sort | remodeling of the cycling transcriptome of the oyster crassostrea gigas by the harmful algae alexandrium minutum |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471176/ https://www.ncbi.nlm.nih.gov/pubmed/28615697 http://dx.doi.org/10.1038/s41598-017-03797-4 |
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