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H(2)O(2) and Ca(2+)-based signaling and associated ion accumulation, antioxidant systems and secondary metabolism orchestrate the response to NaCl stress in perennial ryegrass
Little is known about the interplay between Ca(2+) and H(2)O(2) signaling in stressed cool-season turfgrass. To understand better how Ca(2+) and H(2)O(2) signals are integrated to enhance grass acclimation to stress conditions, we analyzed the rearrangements of endogenous ion accumulation, antioxida...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5090991/ https://www.ncbi.nlm.nih.gov/pubmed/27805022 http://dx.doi.org/10.1038/srep36396 |
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author | Hu, Tao Chen, Ke Hu, Longxing Amombo, Erick Fu, Jinmin |
author_facet | Hu, Tao Chen, Ke Hu, Longxing Amombo, Erick Fu, Jinmin |
author_sort | Hu, Tao |
collection | PubMed |
description | Little is known about the interplay between Ca(2+) and H(2)O(2) signaling in stressed cool-season turfgrass. To understand better how Ca(2+) and H(2)O(2) signals are integrated to enhance grass acclimation to stress conditions, we analyzed the rearrangements of endogenous ion accumulation, antioxidant systems and secondary metabolism in roots, stems and leaves of perennial ryegrass (Lolium perenne L.) treated with exogenous Ca(2+) and H(2)O(2) under salinity. Ca(2+) signaling remarkably enhanced the physiological response to salt conditions. Ca(2+) signaling could maintain ROS homeostasis in stressed grass by increasing the responses of antioxidant genes, proteins and enzymes. H(2)O(2) signaling could activate ROS homeostasis by inducing antioxidant genes but weakened Ca(2+) signaling in leaves. Furthermore, the metabolic profiles revealed that sugars and sugar alcohol accounted for 49.5–88.2% of all metabolites accumulation in all treated leaves and roots. However, the accumulation of these sugars and sugar alcohols displayed opposing trends between Ca(2+) and H(2)O(2) application in salt-stressed plants, which suggests that these metabolites are the common regulatory factor for Ca(2+) and H(2)O(2) signals. These findings assist in understanding better the integrated network in Ca(2+) and H(2)O(2) of cool-season turfgrass’ response to salinity. |
format | Online Article Text |
id | pubmed-5090991 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50909912016-11-08 H(2)O(2) and Ca(2+)-based signaling and associated ion accumulation, antioxidant systems and secondary metabolism orchestrate the response to NaCl stress in perennial ryegrass Hu, Tao Chen, Ke Hu, Longxing Amombo, Erick Fu, Jinmin Sci Rep Article Little is known about the interplay between Ca(2+) and H(2)O(2) signaling in stressed cool-season turfgrass. To understand better how Ca(2+) and H(2)O(2) signals are integrated to enhance grass acclimation to stress conditions, we analyzed the rearrangements of endogenous ion accumulation, antioxidant systems and secondary metabolism in roots, stems and leaves of perennial ryegrass (Lolium perenne L.) treated with exogenous Ca(2+) and H(2)O(2) under salinity. Ca(2+) signaling remarkably enhanced the physiological response to salt conditions. Ca(2+) signaling could maintain ROS homeostasis in stressed grass by increasing the responses of antioxidant genes, proteins and enzymes. H(2)O(2) signaling could activate ROS homeostasis by inducing antioxidant genes but weakened Ca(2+) signaling in leaves. Furthermore, the metabolic profiles revealed that sugars and sugar alcohol accounted for 49.5–88.2% of all metabolites accumulation in all treated leaves and roots. However, the accumulation of these sugars and sugar alcohols displayed opposing trends between Ca(2+) and H(2)O(2) application in salt-stressed plants, which suggests that these metabolites are the common regulatory factor for Ca(2+) and H(2)O(2) signals. These findings assist in understanding better the integrated network in Ca(2+) and H(2)O(2) of cool-season turfgrass’ response to salinity. Nature Publishing Group 2016-11-02 /pmc/articles/PMC5090991/ /pubmed/27805022 http://dx.doi.org/10.1038/srep36396 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Hu, Tao Chen, Ke Hu, Longxing Amombo, Erick Fu, Jinmin H(2)O(2) and Ca(2+)-based signaling and associated ion accumulation, antioxidant systems and secondary metabolism orchestrate the response to NaCl stress in perennial ryegrass |
title | H(2)O(2) and Ca(2+)-based signaling and associated ion accumulation, antioxidant systems and secondary metabolism orchestrate the response to NaCl stress in perennial ryegrass |
title_full | H(2)O(2) and Ca(2+)-based signaling and associated ion accumulation, antioxidant systems and secondary metabolism orchestrate the response to NaCl stress in perennial ryegrass |
title_fullStr | H(2)O(2) and Ca(2+)-based signaling and associated ion accumulation, antioxidant systems and secondary metabolism orchestrate the response to NaCl stress in perennial ryegrass |
title_full_unstemmed | H(2)O(2) and Ca(2+)-based signaling and associated ion accumulation, antioxidant systems and secondary metabolism orchestrate the response to NaCl stress in perennial ryegrass |
title_short | H(2)O(2) and Ca(2+)-based signaling and associated ion accumulation, antioxidant systems and secondary metabolism orchestrate the response to NaCl stress in perennial ryegrass |
title_sort | h(2)o(2) and ca(2+)-based signaling and associated ion accumulation, antioxidant systems and secondary metabolism orchestrate the response to nacl stress in perennial ryegrass |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5090991/ https://www.ncbi.nlm.nih.gov/pubmed/27805022 http://dx.doi.org/10.1038/srep36396 |
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