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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...

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Autores principales: Bickerton, Peter, Sello, Simone, Brownlee, Colin, Pittman, Jon K., Wheeler, Glen L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
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.
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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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