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A sleep-like state in Hydra unravels conserved sleep mechanisms during the evolutionary development of the central nervous system
Sleep behaviors are observed even in nematodes and arthropods, yet little is known about how sleep-regulatory mechanisms have emerged during evolution. Here, we report a sleep-like state in the cnidarian Hydra vulgaris with a primitive nervous organization. Hydra sleep was shaped by homeostasis and...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7541080/ https://www.ncbi.nlm.nih.gov/pubmed/33028524 http://dx.doi.org/10.1126/sciadv.abb9415 |
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author | Kanaya, Hiroyuki J. Park, Sungeon Kim, Ji-hyung Kusumi, Junko Krenenou, Sofian Sawatari, Etsuko Sato, Aya Lee, Jongbin Bang, Hyunwoo Kobayakawa, Yoshitaka Lim, Chunghun Itoh, Taichi Q. |
author_facet | Kanaya, Hiroyuki J. Park, Sungeon Kim, Ji-hyung Kusumi, Junko Krenenou, Sofian Sawatari, Etsuko Sato, Aya Lee, Jongbin Bang, Hyunwoo Kobayakawa, Yoshitaka Lim, Chunghun Itoh, Taichi Q. |
author_sort | Kanaya, Hiroyuki J. |
collection | PubMed |
description | Sleep behaviors are observed even in nematodes and arthropods, yet little is known about how sleep-regulatory mechanisms have emerged during evolution. Here, we report a sleep-like state in the cnidarian Hydra vulgaris with a primitive nervous organization. Hydra sleep was shaped by homeostasis and necessary for cell proliferation, but it lacked free-running circadian rhythms. Instead, we detected 4-hour rhythms that might be generated by ultradian oscillators underlying Hydra sleep. Microarray analysis in sleep-deprived Hydra revealed sleep-dependent expression of 212 genes, including cGMP-dependent protein kinase 1 (PRKG1) and ornithine aminotransferase. Sleep-promoting effects of melatonin, GABA, and PRKG1 were conserved in Hydra. However, arousing dopamine unexpectedly induced Hydra sleep. Opposing effects of ornithine metabolism on sleep were also evident between Hydra and Drosophila, suggesting the evolutionary switch of their sleep-regulatory functions. Thus, sleep-relevant physiology and sleep-regulatory components may have already been acquired at molecular levels in a brain-less metazoan phylum and reprogrammed accordingly. |
format | Online Article Text |
id | pubmed-7541080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-75410802020-10-20 A sleep-like state in Hydra unravels conserved sleep mechanisms during the evolutionary development of the central nervous system Kanaya, Hiroyuki J. Park, Sungeon Kim, Ji-hyung Kusumi, Junko Krenenou, Sofian Sawatari, Etsuko Sato, Aya Lee, Jongbin Bang, Hyunwoo Kobayakawa, Yoshitaka Lim, Chunghun Itoh, Taichi Q. Sci Adv Research Articles Sleep behaviors are observed even in nematodes and arthropods, yet little is known about how sleep-regulatory mechanisms have emerged during evolution. Here, we report a sleep-like state in the cnidarian Hydra vulgaris with a primitive nervous organization. Hydra sleep was shaped by homeostasis and necessary for cell proliferation, but it lacked free-running circadian rhythms. Instead, we detected 4-hour rhythms that might be generated by ultradian oscillators underlying Hydra sleep. Microarray analysis in sleep-deprived Hydra revealed sleep-dependent expression of 212 genes, including cGMP-dependent protein kinase 1 (PRKG1) and ornithine aminotransferase. Sleep-promoting effects of melatonin, GABA, and PRKG1 were conserved in Hydra. However, arousing dopamine unexpectedly induced Hydra sleep. Opposing effects of ornithine metabolism on sleep were also evident between Hydra and Drosophila, suggesting the evolutionary switch of their sleep-regulatory functions. Thus, sleep-relevant physiology and sleep-regulatory components may have already been acquired at molecular levels in a brain-less metazoan phylum and reprogrammed accordingly. American Association for the Advancement of Science 2020-10-07 /pmc/articles/PMC7541080/ /pubmed/33028524 http://dx.doi.org/10.1126/sciadv.abb9415 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Kanaya, Hiroyuki J. Park, Sungeon Kim, Ji-hyung Kusumi, Junko Krenenou, Sofian Sawatari, Etsuko Sato, Aya Lee, Jongbin Bang, Hyunwoo Kobayakawa, Yoshitaka Lim, Chunghun Itoh, Taichi Q. A sleep-like state in Hydra unravels conserved sleep mechanisms during the evolutionary development of the central nervous system |
title | A sleep-like state in Hydra unravels conserved sleep mechanisms during the evolutionary development of the central nervous system |
title_full | A sleep-like state in Hydra unravels conserved sleep mechanisms during the evolutionary development of the central nervous system |
title_fullStr | A sleep-like state in Hydra unravels conserved sleep mechanisms during the evolutionary development of the central nervous system |
title_full_unstemmed | A sleep-like state in Hydra unravels conserved sleep mechanisms during the evolutionary development of the central nervous system |
title_short | A sleep-like state in Hydra unravels conserved sleep mechanisms during the evolutionary development of the central nervous system |
title_sort | sleep-like state in hydra unravels conserved sleep mechanisms during the evolutionary development of the central nervous system |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7541080/ https://www.ncbi.nlm.nih.gov/pubmed/33028524 http://dx.doi.org/10.1126/sciadv.abb9415 |
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