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C. elegans episodic swimming is driven by multifractal kinetics
Fractal scaling is a common property of temporal change in various modes of animal behavior. The molecular mechanisms of fractal scaling in animal behaviors remain largely unexplored. The nematode C. elegans alternates between swimming and resting states in a liquid solution. Here, we report that C....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478975/ https://www.ncbi.nlm.nih.gov/pubmed/32901071 http://dx.doi.org/10.1038/s41598-020-70319-0 |
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author | Ikeda, Yusaku Jurica, Peter Kimura, Hiroshi Takagi, Hiroaki Struzik, Zbigniew R. Kiyono, Ken Arata, Yukinobu Sako, Yasushi |
author_facet | Ikeda, Yusaku Jurica, Peter Kimura, Hiroshi Takagi, Hiroaki Struzik, Zbigniew R. Kiyono, Ken Arata, Yukinobu Sako, Yasushi |
author_sort | Ikeda, Yusaku |
collection | PubMed |
description | Fractal scaling is a common property of temporal change in various modes of animal behavior. The molecular mechanisms of fractal scaling in animal behaviors remain largely unexplored. The nematode C. elegans alternates between swimming and resting states in a liquid solution. Here, we report that C. elegans episodic swimming is characterized by scale-free kinetics with long-range temporal correlation and local temporal clusterization, namely consistent with multifractal kinetics. Residence times in actively-moving and inactive states were distributed in a power law-based scale-free manner. Multifractal analysis showed that temporal correlation and temporal clusterization were distinct between the actively-moving state and the inactive state. These results indicate that C. elegans episodic swimming is driven by transition between two behavioral states, in which each of two transition kinetics follows distinct multifractal kinetics. We found that a conserved behavioral modulator, cyclic GMP dependent kinase (PKG) may regulate the multifractal kinetics underlying an animal behavior. Our combinatorial analysis approach involving molecular genetics and kinetics provides a platform for the molecular dissection of the fractal nature of physiological and behavioral phenomena. |
format | Online Article Text |
id | pubmed-7478975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74789752020-09-11 C. elegans episodic swimming is driven by multifractal kinetics Ikeda, Yusaku Jurica, Peter Kimura, Hiroshi Takagi, Hiroaki Struzik, Zbigniew R. Kiyono, Ken Arata, Yukinobu Sako, Yasushi Sci Rep Article Fractal scaling is a common property of temporal change in various modes of animal behavior. The molecular mechanisms of fractal scaling in animal behaviors remain largely unexplored. The nematode C. elegans alternates between swimming and resting states in a liquid solution. Here, we report that C. elegans episodic swimming is characterized by scale-free kinetics with long-range temporal correlation and local temporal clusterization, namely consistent with multifractal kinetics. Residence times in actively-moving and inactive states were distributed in a power law-based scale-free manner. Multifractal analysis showed that temporal correlation and temporal clusterization were distinct between the actively-moving state and the inactive state. These results indicate that C. elegans episodic swimming is driven by transition between two behavioral states, in which each of two transition kinetics follows distinct multifractal kinetics. We found that a conserved behavioral modulator, cyclic GMP dependent kinase (PKG) may regulate the multifractal kinetics underlying an animal behavior. Our combinatorial analysis approach involving molecular genetics and kinetics provides a platform for the molecular dissection of the fractal nature of physiological and behavioral phenomena. Nature Publishing Group UK 2020-09-08 /pmc/articles/PMC7478975/ /pubmed/32901071 http://dx.doi.org/10.1038/s41598-020-70319-0 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ikeda, Yusaku Jurica, Peter Kimura, Hiroshi Takagi, Hiroaki Struzik, Zbigniew R. Kiyono, Ken Arata, Yukinobu Sako, Yasushi C. elegans episodic swimming is driven by multifractal kinetics |
title | C. elegans episodic swimming is driven by multifractal kinetics |
title_full | C. elegans episodic swimming is driven by multifractal kinetics |
title_fullStr | C. elegans episodic swimming is driven by multifractal kinetics |
title_full_unstemmed | C. elegans episodic swimming is driven by multifractal kinetics |
title_short | C. elegans episodic swimming is driven by multifractal kinetics |
title_sort | c. elegans episodic swimming is driven by multifractal kinetics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478975/ https://www.ncbi.nlm.nih.gov/pubmed/32901071 http://dx.doi.org/10.1038/s41598-020-70319-0 |
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