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Thermotaxis in Chlamydomonas is brought about by membrane excitation and controlled by redox conditions
Temperature is physiologically critical for all living organisms, which cope with temperature stress using metabolic and behavioral responses. In unicellular and some multicellular organisms, thermotaxis is a behavioral response to avoid stressful thermal environments and promote accumulation in an...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6208428/ https://www.ncbi.nlm.nih.gov/pubmed/30382191 http://dx.doi.org/10.1038/s41598-018-34487-4 |
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author | Sekiguchi, Masaya Kameda, Shigetoshi Kurosawa, Satoshi Yoshida, Megumi Yoshimura, Kenjiro |
author_facet | Sekiguchi, Masaya Kameda, Shigetoshi Kurosawa, Satoshi Yoshida, Megumi Yoshimura, Kenjiro |
author_sort | Sekiguchi, Masaya |
collection | PubMed |
description | Temperature is physiologically critical for all living organisms, which cope with temperature stress using metabolic and behavioral responses. In unicellular and some multicellular organisms, thermotaxis is a behavioral response to avoid stressful thermal environments and promote accumulation in an optimal thermal environment. In this study, we examined whether Chlamydomonas reinhardtii, a unicellular green alga, demonstrated thermotaxis. We found that between 10 °C and 30 °C, Chlamydomonas cells migrated toward lower temperatures independent of cultivation temperature. Interestingly, when we applied reagents to change intracellular reduction-oxidation (redox) conditions, we saw that thermotaxis was enhanced, suppressed, or reversed, depending on the redox conditions and cultivation temperature. Thermotaxis was almost absent in ppr2 and ppr3 mutants, which cannot swim backward because of a defect in generating calcium current in flagella. The frequency of spontaneous backward swimming was lower at more favorable temperature, suggesting a pivotal role of spontaneous backward swimming generated by flagellar membrane excitation. |
format | Online Article Text |
id | pubmed-6208428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62084282018-11-01 Thermotaxis in Chlamydomonas is brought about by membrane excitation and controlled by redox conditions Sekiguchi, Masaya Kameda, Shigetoshi Kurosawa, Satoshi Yoshida, Megumi Yoshimura, Kenjiro Sci Rep Article Temperature is physiologically critical for all living organisms, which cope with temperature stress using metabolic and behavioral responses. In unicellular and some multicellular organisms, thermotaxis is a behavioral response to avoid stressful thermal environments and promote accumulation in an optimal thermal environment. In this study, we examined whether Chlamydomonas reinhardtii, a unicellular green alga, demonstrated thermotaxis. We found that between 10 °C and 30 °C, Chlamydomonas cells migrated toward lower temperatures independent of cultivation temperature. Interestingly, when we applied reagents to change intracellular reduction-oxidation (redox) conditions, we saw that thermotaxis was enhanced, suppressed, or reversed, depending on the redox conditions and cultivation temperature. Thermotaxis was almost absent in ppr2 and ppr3 mutants, which cannot swim backward because of a defect in generating calcium current in flagella. The frequency of spontaneous backward swimming was lower at more favorable temperature, suggesting a pivotal role of spontaneous backward swimming generated by flagellar membrane excitation. Nature Publishing Group UK 2018-10-31 /pmc/articles/PMC6208428/ /pubmed/30382191 http://dx.doi.org/10.1038/s41598-018-34487-4 Text en © The Author(s) 2018 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 Sekiguchi, Masaya Kameda, Shigetoshi Kurosawa, Satoshi Yoshida, Megumi Yoshimura, Kenjiro Thermotaxis in Chlamydomonas is brought about by membrane excitation and controlled by redox conditions |
title | Thermotaxis in Chlamydomonas is brought about by membrane excitation and controlled by redox conditions |
title_full | Thermotaxis in Chlamydomonas is brought about by membrane excitation and controlled by redox conditions |
title_fullStr | Thermotaxis in Chlamydomonas is brought about by membrane excitation and controlled by redox conditions |
title_full_unstemmed | Thermotaxis in Chlamydomonas is brought about by membrane excitation and controlled by redox conditions |
title_short | Thermotaxis in Chlamydomonas is brought about by membrane excitation and controlled by redox conditions |
title_sort | thermotaxis in chlamydomonas is brought about by membrane excitation and controlled by redox conditions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6208428/ https://www.ncbi.nlm.nih.gov/pubmed/30382191 http://dx.doi.org/10.1038/s41598-018-34487-4 |
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