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Profiling molecular and behavioral circadian rhythms in the non-symbiotic sea anemone Nematostella vectensis
Endogenous circadian clocks are poorly understood within early-diverging animal lineages. We have characterized circadian behavioral patterns and identified potential components of the circadian clock in the starlet sea anemone, Nematostella vectensis: a model cnidarian which lacks algal symbionts....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4476465/ https://www.ncbi.nlm.nih.gov/pubmed/26081482 http://dx.doi.org/10.1038/srep11418 |
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author | Oren, Matan Tarrant, Ann M. Alon, Shahar Simon-Blecher, Noa Elbaz, Idan Appelbaum, Lior Levy, Oren |
author_facet | Oren, Matan Tarrant, Ann M. Alon, Shahar Simon-Blecher, Noa Elbaz, Idan Appelbaum, Lior Levy, Oren |
author_sort | Oren, Matan |
collection | PubMed |
description | Endogenous circadian clocks are poorly understood within early-diverging animal lineages. We have characterized circadian behavioral patterns and identified potential components of the circadian clock in the starlet sea anemone, Nematostella vectensis: a model cnidarian which lacks algal symbionts. Using automatic video tracking we showed that Nematostella exhibits rhythmic circadian locomotor activity, which is persistent in constant dark, shifted or disrupted by external dark/light cues and maintained the same rate at two different temperatures. This activity was inhibited by a casein kinase 1δ/ε inhibitor, suggesting a role for CK1 homologue(s) in Nematostella clock. Using high-throughput sequencing we profiled Nematostella transcriptomes over 48 hours under a light-dark cycle. We identified 180 Nematostella diurnally-oscillated transcripts and compared them with previously established databases of adult and larvae of the symbiotic coral Acropora millepora, revealing both shared homologues and unique rhythmic genes. Taken together, this study further establishes Nematostella as a non-symbiotic model organism to study circadian rhythms and increases our understanding about the fundamental elements of circadian regulation and their evolution within the Metazoa |
format | Online Article Text |
id | pubmed-4476465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-44764652015-06-24 Profiling molecular and behavioral circadian rhythms in the non-symbiotic sea anemone Nematostella vectensis Oren, Matan Tarrant, Ann M. Alon, Shahar Simon-Blecher, Noa Elbaz, Idan Appelbaum, Lior Levy, Oren Sci Rep Article Endogenous circadian clocks are poorly understood within early-diverging animal lineages. We have characterized circadian behavioral patterns and identified potential components of the circadian clock in the starlet sea anemone, Nematostella vectensis: a model cnidarian which lacks algal symbionts. Using automatic video tracking we showed that Nematostella exhibits rhythmic circadian locomotor activity, which is persistent in constant dark, shifted or disrupted by external dark/light cues and maintained the same rate at two different temperatures. This activity was inhibited by a casein kinase 1δ/ε inhibitor, suggesting a role for CK1 homologue(s) in Nematostella clock. Using high-throughput sequencing we profiled Nematostella transcriptomes over 48 hours under a light-dark cycle. We identified 180 Nematostella diurnally-oscillated transcripts and compared them with previously established databases of adult and larvae of the symbiotic coral Acropora millepora, revealing both shared homologues and unique rhythmic genes. Taken together, this study further establishes Nematostella as a non-symbiotic model organism to study circadian rhythms and increases our understanding about the fundamental elements of circadian regulation and their evolution within the Metazoa Nature Publishing Group 2015-06-17 /pmc/articles/PMC4476465/ /pubmed/26081482 http://dx.doi.org/10.1038/srep11418 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Oren, Matan Tarrant, Ann M. Alon, Shahar Simon-Blecher, Noa Elbaz, Idan Appelbaum, Lior Levy, Oren Profiling molecular and behavioral circadian rhythms in the non-symbiotic sea anemone Nematostella vectensis |
title | Profiling molecular and behavioral circadian rhythms in the non-symbiotic sea anemone
Nematostella vectensis |
title_full | Profiling molecular and behavioral circadian rhythms in the non-symbiotic sea anemone
Nematostella vectensis |
title_fullStr | Profiling molecular and behavioral circadian rhythms in the non-symbiotic sea anemone
Nematostella vectensis |
title_full_unstemmed | Profiling molecular and behavioral circadian rhythms in the non-symbiotic sea anemone
Nematostella vectensis |
title_short | Profiling molecular and behavioral circadian rhythms in the non-symbiotic sea anemone
Nematostella vectensis |
title_sort | profiling molecular and behavioral circadian rhythms in the non-symbiotic sea anemone
nematostella vectensis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4476465/ https://www.ncbi.nlm.nih.gov/pubmed/26081482 http://dx.doi.org/10.1038/srep11418 |
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