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Aequorin-based luminescence imaging reveals differential calcium signalling responses to salt and reactive oxygen species in rice roots

It is well established that both salt and reactive oxygen species (ROS) stresses are able to increase the concentration of cytosolic free Ca(2+) ([Ca(2+)](i)), which is caused by the flux of calcium (Ca(2+)). However, the differences between these two processes are largely unknown. Here, we introduc...

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Autores principales: Zhang, Yanyan, Wang, Yifeng, Taylor, Jemma L., Jiang, Zhonghao, Zhang, Shu, Mei, Fengling, Wu, Yunrong, Wu, Ping, Ni, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986864/
https://www.ncbi.nlm.nih.gov/pubmed/25754405
http://dx.doi.org/10.1093/jxb/erv043
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author Zhang, Yanyan
Wang, Yifeng
Taylor, Jemma L.
Jiang, Zhonghao
Zhang, Shu
Mei, Fengling
Wu, Yunrong
Wu, Ping
Ni, Jun
author_facet Zhang, Yanyan
Wang, Yifeng
Taylor, Jemma L.
Jiang, Zhonghao
Zhang, Shu
Mei, Fengling
Wu, Yunrong
Wu, Ping
Ni, Jun
author_sort Zhang, Yanyan
collection PubMed
description It is well established that both salt and reactive oxygen species (ROS) stresses are able to increase the concentration of cytosolic free Ca(2+) ([Ca(2+)](i)), which is caused by the flux of calcium (Ca(2+)). However, the differences between these two processes are largely unknown. Here, we introduced recombinant aequorin into rice (Oryza sativa) and examined the change in [Ca(2+)](i) in response to salt and ROS stresses. The transgenic rice harbouring aequorin showed strong luminescence in roots when treated with exogenous Ca(2+). Considering the histological differences in roots between rice and Arabidopsis, we reappraised the discharging solution, and suggested that the percentage of ethanol should be 25%. Different concentrations of NaCl induced immediate [Ca(2+)](i) spikes with the same durations and phases. In contrast, H(2)O(2) induced delayed [Ca(2+)](i) spikes with different peaks according to the concentrations of H(2)O(2). According to the Ca(2+) inhibitor research, we also showed that the sources of Ca(2+) induced by NaCl and H(2)O(2) are different. Furthermore, we evaluated the contribution of [Ca(2+)](i) responses in the NaCl- and H(2)O(2)-induced gene expressions respectively, and present a Ca(2+)- and H(2)O(2)-mediated molecular signalling model for the initial response to NaCl in rice.
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spelling pubmed-49868642016-08-22 Aequorin-based luminescence imaging reveals differential calcium signalling responses to salt and reactive oxygen species in rice roots Zhang, Yanyan Wang, Yifeng Taylor, Jemma L. Jiang, Zhonghao Zhang, Shu Mei, Fengling Wu, Yunrong Wu, Ping Ni, Jun J Exp Bot Research Paper It is well established that both salt and reactive oxygen species (ROS) stresses are able to increase the concentration of cytosolic free Ca(2+) ([Ca(2+)](i)), which is caused by the flux of calcium (Ca(2+)). However, the differences between these two processes are largely unknown. Here, we introduced recombinant aequorin into rice (Oryza sativa) and examined the change in [Ca(2+)](i) in response to salt and ROS stresses. The transgenic rice harbouring aequorin showed strong luminescence in roots when treated with exogenous Ca(2+). Considering the histological differences in roots between rice and Arabidopsis, we reappraised the discharging solution, and suggested that the percentage of ethanol should be 25%. Different concentrations of NaCl induced immediate [Ca(2+)](i) spikes with the same durations and phases. In contrast, H(2)O(2) induced delayed [Ca(2+)](i) spikes with different peaks according to the concentrations of H(2)O(2). According to the Ca(2+) inhibitor research, we also showed that the sources of Ca(2+) induced by NaCl and H(2)O(2) are different. Furthermore, we evaluated the contribution of [Ca(2+)](i) responses in the NaCl- and H(2)O(2)-induced gene expressions respectively, and present a Ca(2+)- and H(2)O(2)-mediated molecular signalling model for the initial response to NaCl in rice. Oxford University Press 2015-05 2015-03-09 /pmc/articles/PMC4986864/ /pubmed/25754405 http://dx.doi.org/10.1093/jxb/erv043 Text en © The Author 2015. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Zhang, Yanyan
Wang, Yifeng
Taylor, Jemma L.
Jiang, Zhonghao
Zhang, Shu
Mei, Fengling
Wu, Yunrong
Wu, Ping
Ni, Jun
Aequorin-based luminescence imaging reveals differential calcium signalling responses to salt and reactive oxygen species in rice roots
title Aequorin-based luminescence imaging reveals differential calcium signalling responses to salt and reactive oxygen species in rice roots
title_full Aequorin-based luminescence imaging reveals differential calcium signalling responses to salt and reactive oxygen species in rice roots
title_fullStr Aequorin-based luminescence imaging reveals differential calcium signalling responses to salt and reactive oxygen species in rice roots
title_full_unstemmed Aequorin-based luminescence imaging reveals differential calcium signalling responses to salt and reactive oxygen species in rice roots
title_short Aequorin-based luminescence imaging reveals differential calcium signalling responses to salt and reactive oxygen species in rice roots
title_sort aequorin-based luminescence imaging reveals differential calcium signalling responses to salt and reactive oxygen species in rice roots
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986864/
https://www.ncbi.nlm.nih.gov/pubmed/25754405
http://dx.doi.org/10.1093/jxb/erv043
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