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Cellular pathways during spawning induction in the starlet sea anemone Nematostella vectensis
In cnidarians, long-term ecological success relies on sexual reproduction. The sea anemone Nematostella vectensis, which has emerged as an important model organism for developmental studies, can be induced for spawning by temperature elevation and light exposure. To uncover molecular mechanisms and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8322078/ https://www.ncbi.nlm.nih.gov/pubmed/34326433 http://dx.doi.org/10.1038/s41598-021-95033-3 |
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author | Reuven, Shelly Rinsky, Mieka Brekhman, Vera Malik, Assaf Levy, Oren Lotan, Tamar |
author_facet | Reuven, Shelly Rinsky, Mieka Brekhman, Vera Malik, Assaf Levy, Oren Lotan, Tamar |
author_sort | Reuven, Shelly |
collection | PubMed |
description | In cnidarians, long-term ecological success relies on sexual reproduction. The sea anemone Nematostella vectensis, which has emerged as an important model organism for developmental studies, can be induced for spawning by temperature elevation and light exposure. To uncover molecular mechanisms and pathways underlying spawning, we characterized the transcriptome of Nematostella females before and during spawning induction. We identified an array of processes involving numerous receptors, circadian clock components, cytoskeleton, and extracellular transcripts that are upregulated upon spawning induction. Concurrently, processes related to the cell cycle, fatty acid metabolism, and other housekeeping functions are downregulated. Real-time qPCR revealed that light exposure has a minor effect on expression levels of most examined transcripts, implying that temperature change is a stronger inducer for spawning in Nematostella. Our findings reveal the potential mechanisms that may enable the mesenteries to serve as a gonad-like tissue for the developing oocytes and expand our understanding of sexual reproduction in cnidarians. |
format | Online Article Text |
id | pubmed-8322078 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83220782021-07-30 Cellular pathways during spawning induction in the starlet sea anemone Nematostella vectensis Reuven, Shelly Rinsky, Mieka Brekhman, Vera Malik, Assaf Levy, Oren Lotan, Tamar Sci Rep Article In cnidarians, long-term ecological success relies on sexual reproduction. The sea anemone Nematostella vectensis, which has emerged as an important model organism for developmental studies, can be induced for spawning by temperature elevation and light exposure. To uncover molecular mechanisms and pathways underlying spawning, we characterized the transcriptome of Nematostella females before and during spawning induction. We identified an array of processes involving numerous receptors, circadian clock components, cytoskeleton, and extracellular transcripts that are upregulated upon spawning induction. Concurrently, processes related to the cell cycle, fatty acid metabolism, and other housekeeping functions are downregulated. Real-time qPCR revealed that light exposure has a minor effect on expression levels of most examined transcripts, implying that temperature change is a stronger inducer for spawning in Nematostella. Our findings reveal the potential mechanisms that may enable the mesenteries to serve as a gonad-like tissue for the developing oocytes and expand our understanding of sexual reproduction in cnidarians. Nature Publishing Group UK 2021-07-29 /pmc/articles/PMC8322078/ /pubmed/34326433 http://dx.doi.org/10.1038/s41598-021-95033-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Reuven, Shelly Rinsky, Mieka Brekhman, Vera Malik, Assaf Levy, Oren Lotan, Tamar Cellular pathways during spawning induction in the starlet sea anemone Nematostella vectensis |
title | Cellular pathways during spawning induction in the starlet sea anemone Nematostella vectensis |
title_full | Cellular pathways during spawning induction in the starlet sea anemone Nematostella vectensis |
title_fullStr | Cellular pathways during spawning induction in the starlet sea anemone Nematostella vectensis |
title_full_unstemmed | Cellular pathways during spawning induction in the starlet sea anemone Nematostella vectensis |
title_short | Cellular pathways during spawning induction in the starlet sea anemone Nematostella vectensis |
title_sort | cellular pathways during spawning induction in the starlet sea anemone nematostella vectensis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8322078/ https://www.ncbi.nlm.nih.gov/pubmed/34326433 http://dx.doi.org/10.1038/s41598-021-95033-3 |
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