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Hydrogen sulfide enhances salt tolerance through nitric oxide-mediated maintenance of ion homeostasis in barley seedling roots
Hydrogen sulfide (H(2)S) and nitric oxide (NO) are emerging as messenger molecules involved in the modulation of plant physiological processes. Here, we investigated a signalling network involving H(2)S and NO in salt tolerance pathway of barley. NaHS, a donor of H(2)S, at a low concentration of eit...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4515593/ https://www.ncbi.nlm.nih.gov/pubmed/26213372 http://dx.doi.org/10.1038/srep12516 |
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author | Chen, Juan Wang, Wen-Hua Wu, Fei-Hua He, En-Ming Liu, Xiang Shangguan, Zhou-Ping Zheng, Hai-Lei |
author_facet | Chen, Juan Wang, Wen-Hua Wu, Fei-Hua He, En-Ming Liu, Xiang Shangguan, Zhou-Ping Zheng, Hai-Lei |
author_sort | Chen, Juan |
collection | PubMed |
description | Hydrogen sulfide (H(2)S) and nitric oxide (NO) are emerging as messenger molecules involved in the modulation of plant physiological processes. Here, we investigated a signalling network involving H(2)S and NO in salt tolerance pathway of barley. NaHS, a donor of H(2)S, at a low concentration of either 50 or 100 μM, had significant rescue effects on the 150 mM NaCl-induced inhibition of plant growth and modulated the K(+)/Na(+) balance by decreasing the net K(+) efflux and increasing the gene expression of an inward-rectifying potassium channel (HvAKT1) and a high-affinity K(+) uptake system (HvHAK4). H(2)S and NO maintained the lower Na(+) content in the cytoplast by increasing the amount of PM H(+)-ATPase, the transcriptional levels of PM H(+)-ATPase (HvHA1) and Na(+)/H(+) antiporter (HvSOS1). H(2)S and NO modulated Na(+) compartmentation into the vacuoles with up-regulation of the transcriptional levels of vacuolar Na(+)/H(+) antiporter (HvVNHX2) and H(+)-ATPase subunit β (HvVHA-β) and increased in the protein expression of vacuolar Na(+)/H(+) antiporter (NHE1). H(2)S mimicked the effect of sodium nitroprusside (SNP) by increasing NO production, whereas the function was quenched with the addition of NO scavenger. These results indicated that H(2)S increased salt tolerance by maintaining ion homeostasis, which were mediated by the NO signal. |
format | Online Article Text |
id | pubmed-4515593 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45155932015-07-29 Hydrogen sulfide enhances salt tolerance through nitric oxide-mediated maintenance of ion homeostasis in barley seedling roots Chen, Juan Wang, Wen-Hua Wu, Fei-Hua He, En-Ming Liu, Xiang Shangguan, Zhou-Ping Zheng, Hai-Lei Sci Rep Article Hydrogen sulfide (H(2)S) and nitric oxide (NO) are emerging as messenger molecules involved in the modulation of plant physiological processes. Here, we investigated a signalling network involving H(2)S and NO in salt tolerance pathway of barley. NaHS, a donor of H(2)S, at a low concentration of either 50 or 100 μM, had significant rescue effects on the 150 mM NaCl-induced inhibition of plant growth and modulated the K(+)/Na(+) balance by decreasing the net K(+) efflux and increasing the gene expression of an inward-rectifying potassium channel (HvAKT1) and a high-affinity K(+) uptake system (HvHAK4). H(2)S and NO maintained the lower Na(+) content in the cytoplast by increasing the amount of PM H(+)-ATPase, the transcriptional levels of PM H(+)-ATPase (HvHA1) and Na(+)/H(+) antiporter (HvSOS1). H(2)S and NO modulated Na(+) compartmentation into the vacuoles with up-regulation of the transcriptional levels of vacuolar Na(+)/H(+) antiporter (HvVNHX2) and H(+)-ATPase subunit β (HvVHA-β) and increased in the protein expression of vacuolar Na(+)/H(+) antiporter (NHE1). H(2)S mimicked the effect of sodium nitroprusside (SNP) by increasing NO production, whereas the function was quenched with the addition of NO scavenger. These results indicated that H(2)S increased salt tolerance by maintaining ion homeostasis, which were mediated by the NO signal. Nature Publishing Group 2015-07-27 /pmc/articles/PMC4515593/ /pubmed/26213372 http://dx.doi.org/10.1038/srep12516 Text en Copyright © 2015, Macmillan Publishers Limited 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 Chen, Juan Wang, Wen-Hua Wu, Fei-Hua He, En-Ming Liu, Xiang Shangguan, Zhou-Ping Zheng, Hai-Lei Hydrogen sulfide enhances salt tolerance through nitric oxide-mediated maintenance of ion homeostasis in barley seedling roots |
title | Hydrogen sulfide enhances salt tolerance through nitric oxide-mediated maintenance of ion homeostasis in barley seedling roots |
title_full | Hydrogen sulfide enhances salt tolerance through nitric oxide-mediated maintenance of ion homeostasis in barley seedling roots |
title_fullStr | Hydrogen sulfide enhances salt tolerance through nitric oxide-mediated maintenance of ion homeostasis in barley seedling roots |
title_full_unstemmed | Hydrogen sulfide enhances salt tolerance through nitric oxide-mediated maintenance of ion homeostasis in barley seedling roots |
title_short | Hydrogen sulfide enhances salt tolerance through nitric oxide-mediated maintenance of ion homeostasis in barley seedling roots |
title_sort | hydrogen sulfide enhances salt tolerance through nitric oxide-mediated maintenance of ion homeostasis in barley seedling roots |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4515593/ https://www.ncbi.nlm.nih.gov/pubmed/26213372 http://dx.doi.org/10.1038/srep12516 |
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