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CsPAO4 of Citrus sinensis functions in polyamine terminal catabolism and inhibits plant growth under salt stress
Polyamine oxidase (PAO) is a key enzyme catalyzing polyamine catabolism leading to H(2)O(2) production. We previously demonstrated that Citrus sinensis contains six putative PAO genes, but their functions are not well understood. In this work, we reported functional elucidation of CsPAO4 in polyamin...
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/PMC4989168/ https://www.ncbi.nlm.nih.gov/pubmed/27535697 http://dx.doi.org/10.1038/srep31384 |
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author | Wang, Wei Liu, Ji-Hong |
author_facet | Wang, Wei Liu, Ji-Hong |
author_sort | Wang, Wei |
collection | PubMed |
description | Polyamine oxidase (PAO) is a key enzyme catalyzing polyamine catabolism leading to H(2)O(2) production. We previously demonstrated that Citrus sinensis contains six putative PAO genes, but their functions are not well understood. In this work, we reported functional elucidation of CsPAO4 in polyamine catabolism and salt stress response. CsPAO4 was localized to the apoplast and used both spermidine (Spd) and spermine (Spm) as substrates for terminal catabolism. Transgenic plants overexpressing CsPAO4 displayed prominent increase in PAO activity, concurrent with marked decrease of Spm and Spd and elevation of H(2)O(2). Seeds of transgenic lines displayed better germination when compared with wild type (WT) under salt stress. However, both vegetative growth and root elongation of the transgenic lines were prominently inhibited under salt stress, accompanied by higher level of H(2)O(2) and more conspicuous programmed cell death (PCD). Exogenous supply of catalase (CAT), a H(2)O(2) scavenger, partially recovered the vegetative growth and root elongation. In addition, spermine inhibited root growth of transgenic plants. Taken together, these data demonstrated that CsPAO4 accounts for production of H(2)O(2) causing oxidative damages under salt stress and that down-regulation of a PAO gene involved in polyamine terminal catabolism may be an alternative approach for improving salt stress tolerance. |
format | Online Article Text |
id | pubmed-4989168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49891682016-08-30 CsPAO4 of Citrus sinensis functions in polyamine terminal catabolism and inhibits plant growth under salt stress Wang, Wei Liu, Ji-Hong Sci Rep Article Polyamine oxidase (PAO) is a key enzyme catalyzing polyamine catabolism leading to H(2)O(2) production. We previously demonstrated that Citrus sinensis contains six putative PAO genes, but their functions are not well understood. In this work, we reported functional elucidation of CsPAO4 in polyamine catabolism and salt stress response. CsPAO4 was localized to the apoplast and used both spermidine (Spd) and spermine (Spm) as substrates for terminal catabolism. Transgenic plants overexpressing CsPAO4 displayed prominent increase in PAO activity, concurrent with marked decrease of Spm and Spd and elevation of H(2)O(2). Seeds of transgenic lines displayed better germination when compared with wild type (WT) under salt stress. However, both vegetative growth and root elongation of the transgenic lines were prominently inhibited under salt stress, accompanied by higher level of H(2)O(2) and more conspicuous programmed cell death (PCD). Exogenous supply of catalase (CAT), a H(2)O(2) scavenger, partially recovered the vegetative growth and root elongation. In addition, spermine inhibited root growth of transgenic plants. Taken together, these data demonstrated that CsPAO4 accounts for production of H(2)O(2) causing oxidative damages under salt stress and that down-regulation of a PAO gene involved in polyamine terminal catabolism may be an alternative approach for improving salt stress tolerance. Nature Publishing Group 2016-08-18 /pmc/articles/PMC4989168/ /pubmed/27535697 http://dx.doi.org/10.1038/srep31384 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 Wang, Wei Liu, Ji-Hong CsPAO4 of Citrus sinensis functions in polyamine terminal catabolism and inhibits plant growth under salt stress |
title | CsPAO4 of Citrus sinensis functions in polyamine terminal catabolism and inhibits plant growth under salt stress |
title_full | CsPAO4 of Citrus sinensis functions in polyamine terminal catabolism and inhibits plant growth under salt stress |
title_fullStr | CsPAO4 of Citrus sinensis functions in polyamine terminal catabolism and inhibits plant growth under salt stress |
title_full_unstemmed | CsPAO4 of Citrus sinensis functions in polyamine terminal catabolism and inhibits plant growth under salt stress |
title_short | CsPAO4 of Citrus sinensis functions in polyamine terminal catabolism and inhibits plant growth under salt stress |
title_sort | cspao4 of citrus sinensis functions in polyamine terminal catabolism and inhibits plant growth under salt stress |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4989168/ https://www.ncbi.nlm.nih.gov/pubmed/27535697 http://dx.doi.org/10.1038/srep31384 |
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