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Timing of embryonic quiescence determines viability of embryos from the calanoid copepod, Acartia tonsa (Dana)

Like 41 other calanoid copepods, Acartia tonsa, are capable of inducing embryonic quiescence when experiencing unfavorable environmental conditions. The ecdysone-signaling cascade is known to have a key function in developmental processes like embryogenesis and molting of arthropods, including copep...

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Autores principales: Nilsson, Birgitte, Hansen, Benni Winding
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5841787/
https://www.ncbi.nlm.nih.gov/pubmed/29513715
http://dx.doi.org/10.1371/journal.pone.0193727
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author Nilsson, Birgitte
Hansen, Benni Winding
author_facet Nilsson, Birgitte
Hansen, Benni Winding
author_sort Nilsson, Birgitte
collection PubMed
description Like 41 other calanoid copepods, Acartia tonsa, are capable of inducing embryonic quiescence when experiencing unfavorable environmental conditions. The ecdysone-signaling cascade is known to have a key function in developmental processes like embryogenesis and molting of arthropods, including copepods. We examined the role of ecdysteroid-phosphate phosphatase (EPPase), ecdysone receptor (EcR), ß fushi tarazu transcription factor 1 (ßFTZ-F1), and the ecdysteroid-regulated early gene E74 (E74), which represent different levels of the ecdysone-signaling cascade in our calanoid model organism. Progression of embryogenesis was monitored and hatching success determined to evaluate viability. Embryos that were induced quiescence before the gastrulation stage would stay in gastrulation during the rest of quiescence and exhibited a slower pace of hatching as compared to subitaneous embryos. In contrast, embryos developed further than gastrulation would stay in gastrulation or later stages during quiescence and showed a rapid pace in hatching after quiescence termination. Expression patterns suggested two peaks of the biological active ecdysteroids, 20-hydroxyecdysone (20E). The first peak of 20E was expressed in concert with the beginning of embryogenesis originating from yolk-conjugated ecdysteroids, based on EPPase expression. The second peak is suggested to originate from de novo synthesized 20E around the limb bud stage. During quiescence, the expression patterns of EPPase, EcR, ßFTZ-F1, and E74 were either decreasing or not changing over time. This suggests that the ecdysone-signaling pathway play a key role in the subitaneous development of A. tonsa embryogenesis, but not during quiescence. The observation is of profound ecological and practical relevance for the dynamics of egg banks.
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spelling pubmed-58417872018-03-23 Timing of embryonic quiescence determines viability of embryos from the calanoid copepod, Acartia tonsa (Dana) Nilsson, Birgitte Hansen, Benni Winding PLoS One Research Article Like 41 other calanoid copepods, Acartia tonsa, are capable of inducing embryonic quiescence when experiencing unfavorable environmental conditions. The ecdysone-signaling cascade is known to have a key function in developmental processes like embryogenesis and molting of arthropods, including copepods. We examined the role of ecdysteroid-phosphate phosphatase (EPPase), ecdysone receptor (EcR), ß fushi tarazu transcription factor 1 (ßFTZ-F1), and the ecdysteroid-regulated early gene E74 (E74), which represent different levels of the ecdysone-signaling cascade in our calanoid model organism. Progression of embryogenesis was monitored and hatching success determined to evaluate viability. Embryos that were induced quiescence before the gastrulation stage would stay in gastrulation during the rest of quiescence and exhibited a slower pace of hatching as compared to subitaneous embryos. In contrast, embryos developed further than gastrulation would stay in gastrulation or later stages during quiescence and showed a rapid pace in hatching after quiescence termination. Expression patterns suggested two peaks of the biological active ecdysteroids, 20-hydroxyecdysone (20E). The first peak of 20E was expressed in concert with the beginning of embryogenesis originating from yolk-conjugated ecdysteroids, based on EPPase expression. The second peak is suggested to originate from de novo synthesized 20E around the limb bud stage. During quiescence, the expression patterns of EPPase, EcR, ßFTZ-F1, and E74 were either decreasing or not changing over time. This suggests that the ecdysone-signaling pathway play a key role in the subitaneous development of A. tonsa embryogenesis, but not during quiescence. The observation is of profound ecological and practical relevance for the dynamics of egg banks. Public Library of Science 2018-03-07 /pmc/articles/PMC5841787/ /pubmed/29513715 http://dx.doi.org/10.1371/journal.pone.0193727 Text en © 2018 Nilsson, Hansen http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Nilsson, Birgitte
Hansen, Benni Winding
Timing of embryonic quiescence determines viability of embryos from the calanoid copepod, Acartia tonsa (Dana)
title Timing of embryonic quiescence determines viability of embryos from the calanoid copepod, Acartia tonsa (Dana)
title_full Timing of embryonic quiescence determines viability of embryos from the calanoid copepod, Acartia tonsa (Dana)
title_fullStr Timing of embryonic quiescence determines viability of embryos from the calanoid copepod, Acartia tonsa (Dana)
title_full_unstemmed Timing of embryonic quiescence determines viability of embryos from the calanoid copepod, Acartia tonsa (Dana)
title_short Timing of embryonic quiescence determines viability of embryos from the calanoid copepod, Acartia tonsa (Dana)
title_sort timing of embryonic quiescence determines viability of embryos from the calanoid copepod, acartia tonsa (dana)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5841787/
https://www.ncbi.nlm.nih.gov/pubmed/29513715
http://dx.doi.org/10.1371/journal.pone.0193727
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