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Tidal and diel orchestration of behaviour and gene expression in an intertidal mollusc

Intertidal inhabitants are exposed to the 24-hour solar day, and the 12.4 hour rising and falling of the tides. One or both of these cycles govern intertidal organisms’ behaviour and physiology, yet little is known about the molecular clockworks of tidal rhythmicity. Here, we show that the limpet Ce...

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Autores principales: Schnytzer, Y., Simon-Blecher, N., Li, J., Waldman Ben-Asher, H., Salmon-Divon, M., Achituv, Y., Hughes, M. E., Levy, O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5861051/
https://www.ncbi.nlm.nih.gov/pubmed/29559663
http://dx.doi.org/10.1038/s41598-018-23167-y
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author Schnytzer, Y.
Simon-Blecher, N.
Li, J.
Waldman Ben-Asher, H.
Salmon-Divon, M.
Achituv, Y.
Hughes, M. E.
Levy, O.
author_facet Schnytzer, Y.
Simon-Blecher, N.
Li, J.
Waldman Ben-Asher, H.
Salmon-Divon, M.
Achituv, Y.
Hughes, M. E.
Levy, O.
author_sort Schnytzer, Y.
collection PubMed
description Intertidal inhabitants are exposed to the 24-hour solar day, and the 12.4 hour rising and falling of the tides. One or both of these cycles govern intertidal organisms’ behaviour and physiology, yet little is known about the molecular clockworks of tidal rhythmicity. Here, we show that the limpet Cellana rota exhibits robust tidally rhythmic behaviour and gene expression. We assembled a de-novo transcriptome, identifying novel tidal, along with known circadian clock genes. Surprisingly, most of the putative circadian clock genes, lack a typical rhythmicity. We identified numerous tidally rhythmic genes and pathways commonly associated with the circadian clock. We show that not only is the behaviour of an intertidal organism in tune with the tides, but so too are many of its genes and pathways. These findings highlight the plasticity of biological timekeeping in nature, strengthening the growing notion that the role of ‘canonical’ circadian clock genes may be more fluid than previously thought, as exhibited in an organism which has evolved in an environment where tidal oscillations are the dominant driving force.
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spelling pubmed-58610512018-03-26 Tidal and diel orchestration of behaviour and gene expression in an intertidal mollusc Schnytzer, Y. Simon-Blecher, N. Li, J. Waldman Ben-Asher, H. Salmon-Divon, M. Achituv, Y. Hughes, M. E. Levy, O. Sci Rep Article Intertidal inhabitants are exposed to the 24-hour solar day, and the 12.4 hour rising and falling of the tides. One or both of these cycles govern intertidal organisms’ behaviour and physiology, yet little is known about the molecular clockworks of tidal rhythmicity. Here, we show that the limpet Cellana rota exhibits robust tidally rhythmic behaviour and gene expression. We assembled a de-novo transcriptome, identifying novel tidal, along with known circadian clock genes. Surprisingly, most of the putative circadian clock genes, lack a typical rhythmicity. We identified numerous tidally rhythmic genes and pathways commonly associated with the circadian clock. We show that not only is the behaviour of an intertidal organism in tune with the tides, but so too are many of its genes and pathways. These findings highlight the plasticity of biological timekeeping in nature, strengthening the growing notion that the role of ‘canonical’ circadian clock genes may be more fluid than previously thought, as exhibited in an organism which has evolved in an environment where tidal oscillations are the dominant driving force. Nature Publishing Group UK 2018-03-20 /pmc/articles/PMC5861051/ /pubmed/29559663 http://dx.doi.org/10.1038/s41598-018-23167-y Text en © The Author(s) 2018 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
Schnytzer, Y.
Simon-Blecher, N.
Li, J.
Waldman Ben-Asher, H.
Salmon-Divon, M.
Achituv, Y.
Hughes, M. E.
Levy, O.
Tidal and diel orchestration of behaviour and gene expression in an intertidal mollusc
title Tidal and diel orchestration of behaviour and gene expression in an intertidal mollusc
title_full Tidal and diel orchestration of behaviour and gene expression in an intertidal mollusc
title_fullStr Tidal and diel orchestration of behaviour and gene expression in an intertidal mollusc
title_full_unstemmed Tidal and diel orchestration of behaviour and gene expression in an intertidal mollusc
title_short Tidal and diel orchestration of behaviour and gene expression in an intertidal mollusc
title_sort tidal and diel orchestration of behaviour and gene expression in an intertidal mollusc
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5861051/
https://www.ncbi.nlm.nih.gov/pubmed/29559663
http://dx.doi.org/10.1038/s41598-018-23167-y
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