Cargando…

Finding Nemo’s clock reveals switch from nocturnal to diurnal activity

Timing mechanisms play a key role in the biology of coral reef fish. Typically, fish larvae leave their reef after hatching, stay for a period in the open ocean before returning to the reef for settlement. During this dispersal, larvae use a time-compensated sun compass for orientation. However, the...

Descripción completa

Detalles Bibliográficos
Autores principales: Schalm, Gregor, Bruns, Kristina, Drachenberg, Nina, Geyer, Nathalie, Foulkes, Nicholas S., Bertolucci, Cristiano, Gerlach, Gabriele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7990958/
https://www.ncbi.nlm.nih.gov/pubmed/33762724
http://dx.doi.org/10.1038/s41598-021-86244-9
_version_ 1783669159448543232
author Schalm, Gregor
Bruns, Kristina
Drachenberg, Nina
Geyer, Nathalie
Foulkes, Nicholas S.
Bertolucci, Cristiano
Gerlach, Gabriele
author_facet Schalm, Gregor
Bruns, Kristina
Drachenberg, Nina
Geyer, Nathalie
Foulkes, Nicholas S.
Bertolucci, Cristiano
Gerlach, Gabriele
author_sort Schalm, Gregor
collection PubMed
description Timing mechanisms play a key role in the biology of coral reef fish. Typically, fish larvae leave their reef after hatching, stay for a period in the open ocean before returning to the reef for settlement. During this dispersal, larvae use a time-compensated sun compass for orientation. However, the timing of settlement and how coral reef fish keep track of time via endogenous timing mechanisms is poorly understood. Here, we have studied the behavioural and genetic basis of diel rhythms in the clown anemonefish Amphiprion ocellaris. We document a behavioural shift from nocturnal larvae to diurnal adults, while juveniles show an intermediate pattern of activity which potentially indicates flexibility in the timing of settlement on a host anemone. qRTPCR analysis of six core circadian clock genes (bmal1, clocka, cry1b, per1b, per2, per3) reveals rhythmic gene expression patterns that are comparable in larvae and juveniles, and so do not reflect the corresponding activity changes. By establishing an embryonic cell line, we demonstrate that clown anemonefish possess an endogenous clock with similar properties to that of the zebrafish circadian clock. Furthermore, our study provides a first basis to study the multi-layered interaction of clocks from fish, anemones and their zooxanthellae endosymbionts.
format Online
Article
Text
id pubmed-7990958
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-79909582021-03-26 Finding Nemo’s clock reveals switch from nocturnal to diurnal activity Schalm, Gregor Bruns, Kristina Drachenberg, Nina Geyer, Nathalie Foulkes, Nicholas S. Bertolucci, Cristiano Gerlach, Gabriele Sci Rep Article Timing mechanisms play a key role in the biology of coral reef fish. Typically, fish larvae leave their reef after hatching, stay for a period in the open ocean before returning to the reef for settlement. During this dispersal, larvae use a time-compensated sun compass for orientation. However, the timing of settlement and how coral reef fish keep track of time via endogenous timing mechanisms is poorly understood. Here, we have studied the behavioural and genetic basis of diel rhythms in the clown anemonefish Amphiprion ocellaris. We document a behavioural shift from nocturnal larvae to diurnal adults, while juveniles show an intermediate pattern of activity which potentially indicates flexibility in the timing of settlement on a host anemone. qRTPCR analysis of six core circadian clock genes (bmal1, clocka, cry1b, per1b, per2, per3) reveals rhythmic gene expression patterns that are comparable in larvae and juveniles, and so do not reflect the corresponding activity changes. By establishing an embryonic cell line, we demonstrate that clown anemonefish possess an endogenous clock with similar properties to that of the zebrafish circadian clock. Furthermore, our study provides a first basis to study the multi-layered interaction of clocks from fish, anemones and their zooxanthellae endosymbionts. Nature Publishing Group UK 2021-03-24 /pmc/articles/PMC7990958/ /pubmed/33762724 http://dx.doi.org/10.1038/s41598-021-86244-9 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Schalm, Gregor
Bruns, Kristina
Drachenberg, Nina
Geyer, Nathalie
Foulkes, Nicholas S.
Bertolucci, Cristiano
Gerlach, Gabriele
Finding Nemo’s clock reveals switch from nocturnal to diurnal activity
title Finding Nemo’s clock reveals switch from nocturnal to diurnal activity
title_full Finding Nemo’s clock reveals switch from nocturnal to diurnal activity
title_fullStr Finding Nemo’s clock reveals switch from nocturnal to diurnal activity
title_full_unstemmed Finding Nemo’s clock reveals switch from nocturnal to diurnal activity
title_short Finding Nemo’s clock reveals switch from nocturnal to diurnal activity
title_sort finding nemo’s clock reveals switch from nocturnal to diurnal activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7990958/
https://www.ncbi.nlm.nih.gov/pubmed/33762724
http://dx.doi.org/10.1038/s41598-021-86244-9
work_keys_str_mv AT schalmgregor findingnemosclockrevealsswitchfromnocturnaltodiurnalactivity
AT brunskristina findingnemosclockrevealsswitchfromnocturnaltodiurnalactivity
AT drachenbergnina findingnemosclockrevealsswitchfromnocturnaltodiurnalactivity
AT geyernathalie findingnemosclockrevealsswitchfromnocturnaltodiurnalactivity
AT foulkesnicholass findingnemosclockrevealsswitchfromnocturnaltodiurnalactivity
AT bertoluccicristiano findingnemosclockrevealsswitchfromnocturnaltodiurnalactivity
AT gerlachgabriele findingnemosclockrevealsswitchfromnocturnaltodiurnalactivity