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Post-diapause transcriptomic restarts: insight from a high-latitude copepod

BACKGROUND: Diapause is a seasonal dormancy that allows organisms to survive unfavorable conditions and optimizes the timing of reproduction and growth. Emergence from diapause reverses the state of arrested development and metabolic suppression returning the organism to an active state. The physiol...

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Autores principales: Roncalli, Vittoria, Cieslak, Matthew C., Castelfranco, Ann M., Hopcroft, Russell R., Hartline, Daniel K., Lenz, Petra H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8176732/
https://www.ncbi.nlm.nih.gov/pubmed/34082716
http://dx.doi.org/10.1186/s12864-021-07557-7
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author Roncalli, Vittoria
Cieslak, Matthew C.
Castelfranco, Ann M.
Hopcroft, Russell R.
Hartline, Daniel K.
Lenz, Petra H.
author_facet Roncalli, Vittoria
Cieslak, Matthew C.
Castelfranco, Ann M.
Hopcroft, Russell R.
Hartline, Daniel K.
Lenz, Petra H.
author_sort Roncalli, Vittoria
collection PubMed
description BACKGROUND: Diapause is a seasonal dormancy that allows organisms to survive unfavorable conditions and optimizes the timing of reproduction and growth. Emergence from diapause reverses the state of arrested development and metabolic suppression returning the organism to an active state. The physiological mechanisms that regulate the transition from diapause to post-diapause are still unknown. In this study, this transition has been characterized for the sub-arctic calanoid copepod Neocalanus flemingeri, a key crustacean zooplankter that supports the highly productive North Pacific fisheries. Transcriptional profiling of females, determined over a two-week time series starting with diapausing females collected from > 400 m depth, characterized the molecular mechanisms that regulate the post-diapause trajectory. RESULTS: A complex set of transitions in relative gene expression defined the transcriptomic changes from diapause to post-diapause. Despite low temperatures (5–6 °C), the switch from a “diapause” to a “post-diapause” transcriptional profile occurred within 12 h of the termination stimulus. Transcriptional changes signaling the end of diapause were activated within one-hour post collection and included the up-regulation of genes involved in the 20E cascade pathway, the TCA cycle and RNA metabolism in combination with the down-regulation of genes associated with chromatin silencing. By 12 h, females exhibited a post-diapause phenotype characterized by the up-regulation of genes involved in cell division, cell differentiation and multiple developmental processes. By seven days post collection, the reproductive program was fully activated as indicated by up-regulation of genes involved in oogenesis and energy metabolism, processes that were enriched among the differentially expressed genes. CONCLUSIONS: The analysis revealed a finely structured, precisely orchestrated sequence of transcriptional changes that led to rapid changes in the activation of biological processes paving the way to the successful completion of the reproductive program. Our findings lead to new hypotheses related to potentially universal mechanisms that terminate diapause before an organism can resume its developmental program. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07557-7.
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spelling pubmed-81767322021-06-04 Post-diapause transcriptomic restarts: insight from a high-latitude copepod Roncalli, Vittoria Cieslak, Matthew C. Castelfranco, Ann M. Hopcroft, Russell R. Hartline, Daniel K. Lenz, Petra H. BMC Genomics Research Article BACKGROUND: Diapause is a seasonal dormancy that allows organisms to survive unfavorable conditions and optimizes the timing of reproduction and growth. Emergence from diapause reverses the state of arrested development and metabolic suppression returning the organism to an active state. The physiological mechanisms that regulate the transition from diapause to post-diapause are still unknown. In this study, this transition has been characterized for the sub-arctic calanoid copepod Neocalanus flemingeri, a key crustacean zooplankter that supports the highly productive North Pacific fisheries. Transcriptional profiling of females, determined over a two-week time series starting with diapausing females collected from > 400 m depth, characterized the molecular mechanisms that regulate the post-diapause trajectory. RESULTS: A complex set of transitions in relative gene expression defined the transcriptomic changes from diapause to post-diapause. Despite low temperatures (5–6 °C), the switch from a “diapause” to a “post-diapause” transcriptional profile occurred within 12 h of the termination stimulus. Transcriptional changes signaling the end of diapause were activated within one-hour post collection and included the up-regulation of genes involved in the 20E cascade pathway, the TCA cycle and RNA metabolism in combination with the down-regulation of genes associated with chromatin silencing. By 12 h, females exhibited a post-diapause phenotype characterized by the up-regulation of genes involved in cell division, cell differentiation and multiple developmental processes. By seven days post collection, the reproductive program was fully activated as indicated by up-regulation of genes involved in oogenesis and energy metabolism, processes that were enriched among the differentially expressed genes. CONCLUSIONS: The analysis revealed a finely structured, precisely orchestrated sequence of transcriptional changes that led to rapid changes in the activation of biological processes paving the way to the successful completion of the reproductive program. Our findings lead to new hypotheses related to potentially universal mechanisms that terminate diapause before an organism can resume its developmental program. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07557-7. BioMed Central 2021-06-03 /pmc/articles/PMC8176732/ /pubmed/34082716 http://dx.doi.org/10.1186/s12864-021-07557-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Roncalli, Vittoria
Cieslak, Matthew C.
Castelfranco, Ann M.
Hopcroft, Russell R.
Hartline, Daniel K.
Lenz, Petra H.
Post-diapause transcriptomic restarts: insight from a high-latitude copepod
title Post-diapause transcriptomic restarts: insight from a high-latitude copepod
title_full Post-diapause transcriptomic restarts: insight from a high-latitude copepod
title_fullStr Post-diapause transcriptomic restarts: insight from a high-latitude copepod
title_full_unstemmed Post-diapause transcriptomic restarts: insight from a high-latitude copepod
title_short Post-diapause transcriptomic restarts: insight from a high-latitude copepod
title_sort post-diapause transcriptomic restarts: insight from a high-latitude copepod
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8176732/
https://www.ncbi.nlm.nih.gov/pubmed/34082716
http://dx.doi.org/10.1186/s12864-021-07557-7
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