Cargando…

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....

Descripción completa

Detalles Bibliográficos
Autores principales: Oren, Matan, Tarrant, Ann M., Alon, Shahar, Simon-Blecher, Noa, Elbaz, Idan, Appelbaum, Lior, Levy, Oren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
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
_version_ 1782377603933405184
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
work_keys_str_mv AT orenmatan profilingmolecularandbehavioralcircadianrhythmsinthenonsymbioticseaanemonenematostellavectensis
AT tarrantannm profilingmolecularandbehavioralcircadianrhythmsinthenonsymbioticseaanemonenematostellavectensis
AT alonshahar profilingmolecularandbehavioralcircadianrhythmsinthenonsymbioticseaanemonenematostellavectensis
AT simonblechernoa profilingmolecularandbehavioralcircadianrhythmsinthenonsymbioticseaanemonenematostellavectensis
AT elbazidan profilingmolecularandbehavioralcircadianrhythmsinthenonsymbioticseaanemonenematostellavectensis
AT appelbaumlior profilingmolecularandbehavioralcircadianrhythmsinthenonsymbioticseaanemonenematostellavectensis
AT levyoren profilingmolecularandbehavioralcircadianrhythmsinthenonsymbioticseaanemonenematostellavectensis