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Spatial and temporal specificity of Ca(2+) signalling in Chlamydomonas reinhardtii in response to osmotic stress
Ca(2+)‐dependent signalling processes enable plants to perceive and respond to diverse environmental stressors, such as osmotic stress. A clear understanding of the role of spatiotemporal Ca(2+) signalling in green algal lineages is necessary in order to understand how the Ca(2+) signalling machiner...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5111745/ https://www.ncbi.nlm.nih.gov/pubmed/27516045 http://dx.doi.org/10.1111/nph.14128 |
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author | Bickerton, Peter Sello, Simone Brownlee, Colin Pittman, Jon K. Wheeler, Glen L. |
author_facet | Bickerton, Peter Sello, Simone Brownlee, Colin Pittman, Jon K. Wheeler, Glen L. |
author_sort | Bickerton, Peter |
collection | PubMed |
description | Ca(2+)‐dependent signalling processes enable plants to perceive and respond to diverse environmental stressors, such as osmotic stress. A clear understanding of the role of spatiotemporal Ca(2+) signalling in green algal lineages is necessary in order to understand how the Ca(2+) signalling machinery has evolved in land plants. We used single‐cell imaging of Ca(2+)‐responsive fluorescent dyes in the unicellular green alga Chlamydomonas reinhardtii to examine the specificity of spatial and temporal dynamics of Ca(2+) elevations in the cytosol and flagella in response to salinity and osmotic stress. We found that salt stress induced a single Ca(2+) elevation that was modulated by the strength of the stimulus and originated in the apex of the cell, spreading as a fast Ca(2+) wave. By contrast, hypo‐osmotic stress induced a series of repetitive Ca(2+) elevations in the cytosol that were spatially uniform. Hypo‐osmotic stimuli also induced Ca(2+) elevations in the flagella that occurred independently from those in the cytosol. Our results indicate that the requirement for Ca(2+) signalling in response to osmotic stress is conserved between land plants and green algae, but the distinct spatial and temporal dynamics of osmotic Ca(2+) elevations in C. reinhardtii suggest important mechanistic differences between the two lineages. |
format | Online Article Text |
id | pubmed-5111745 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-51117452016-11-16 Spatial and temporal specificity of Ca(2+) signalling in Chlamydomonas reinhardtii in response to osmotic stress Bickerton, Peter Sello, Simone Brownlee, Colin Pittman, Jon K. Wheeler, Glen L. New Phytol Research Ca(2+)‐dependent signalling processes enable plants to perceive and respond to diverse environmental stressors, such as osmotic stress. A clear understanding of the role of spatiotemporal Ca(2+) signalling in green algal lineages is necessary in order to understand how the Ca(2+) signalling machinery has evolved in land plants. We used single‐cell imaging of Ca(2+)‐responsive fluorescent dyes in the unicellular green alga Chlamydomonas reinhardtii to examine the specificity of spatial and temporal dynamics of Ca(2+) elevations in the cytosol and flagella in response to salinity and osmotic stress. We found that salt stress induced a single Ca(2+) elevation that was modulated by the strength of the stimulus and originated in the apex of the cell, spreading as a fast Ca(2+) wave. By contrast, hypo‐osmotic stress induced a series of repetitive Ca(2+) elevations in the cytosol that were spatially uniform. Hypo‐osmotic stimuli also induced Ca(2+) elevations in the flagella that occurred independently from those in the cytosol. Our results indicate that the requirement for Ca(2+) signalling in response to osmotic stress is conserved between land plants and green algae, but the distinct spatial and temporal dynamics of osmotic Ca(2+) elevations in C. reinhardtii suggest important mechanistic differences between the two lineages. John Wiley and Sons Inc. 2016-08-12 2016-12 /pmc/articles/PMC5111745/ /pubmed/27516045 http://dx.doi.org/10.1111/nph.14128 Text en © 2016 The Authors. New Phytologist © 2016 New Phytologist Trust This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Bickerton, Peter Sello, Simone Brownlee, Colin Pittman, Jon K. Wheeler, Glen L. Spatial and temporal specificity of Ca(2+) signalling in Chlamydomonas reinhardtii in response to osmotic stress |
title | Spatial and temporal specificity of Ca(2+) signalling in Chlamydomonas reinhardtii in response to osmotic stress |
title_full | Spatial and temporal specificity of Ca(2+) signalling in Chlamydomonas reinhardtii in response to osmotic stress |
title_fullStr | Spatial and temporal specificity of Ca(2+) signalling in Chlamydomonas reinhardtii in response to osmotic stress |
title_full_unstemmed | Spatial and temporal specificity of Ca(2+) signalling in Chlamydomonas reinhardtii in response to osmotic stress |
title_short | Spatial and temporal specificity of Ca(2+) signalling in Chlamydomonas reinhardtii in response to osmotic stress |
title_sort | spatial and temporal specificity of ca(2+) signalling in chlamydomonas reinhardtii in response to osmotic stress |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5111745/ https://www.ncbi.nlm.nih.gov/pubmed/27516045 http://dx.doi.org/10.1111/nph.14128 |
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