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Dual regulation of water retention and cell growth by a stress-associated protein (SAP) gene in Prunus
We have identified a gene (PpSAP1) of Prunus persica coding for a stress-associated protein (SAP) containing Zn-finger domains A20 and AN1. SAPs have been described as regulators of the abiotic stress response in plant species, emerging as potential candidates for improvement of stress tolerance in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428470/ https://www.ncbi.nlm.nih.gov/pubmed/28336950 http://dx.doi.org/10.1038/s41598-017-00471-7 |
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author | Lloret, Alba Conejero, Ana Leida, Carmen Petri, César Gil-Muñoz, Francisco Burgos, Lorenzo Badenes, María Luisa Ríos, Gabino |
author_facet | Lloret, Alba Conejero, Ana Leida, Carmen Petri, César Gil-Muñoz, Francisco Burgos, Lorenzo Badenes, María Luisa Ríos, Gabino |
author_sort | Lloret, Alba |
collection | PubMed |
description | We have identified a gene (PpSAP1) of Prunus persica coding for a stress-associated protein (SAP) containing Zn-finger domains A20 and AN1. SAPs have been described as regulators of the abiotic stress response in plant species, emerging as potential candidates for improvement of stress tolerance in plants. PpSAP1 was highly expressed in leaves and dormant buds, being down-regulated before bud dormancy release. PpSAP1 expression was moderately induced by water stresses and heat in buds. In addition, it was found that PpSAP1 strongly interacts with polyubiquitin proteins in the yeast two-hybrid system. The overexpression of PpSAP1 in transgenic plum plants led to alterations in leaf shape and an increase of water retention under drought stress. Moreover, we established that leaf morphological alterations were concomitant with a reduced cell size and down-regulation of genes involved in cell growth, such as GROWTH-REGULATING FACTOR (GRF)1-like, TONOPLAST INTRINSIC PROTEIN (TIP)-like, and TARGET OF RAPAMYCIN (TOR)-like. Especially, the inverse expression pattern of PpSAP1 and TOR-like in transgenic plum and peach buds suggests a role of PpSAP1 in cell expansion through the regulation of TOR pathway. |
format | Online Article Text |
id | pubmed-5428470 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54284702017-05-15 Dual regulation of water retention and cell growth by a stress-associated protein (SAP) gene in Prunus Lloret, Alba Conejero, Ana Leida, Carmen Petri, César Gil-Muñoz, Francisco Burgos, Lorenzo Badenes, María Luisa Ríos, Gabino Sci Rep Article We have identified a gene (PpSAP1) of Prunus persica coding for a stress-associated protein (SAP) containing Zn-finger domains A20 and AN1. SAPs have been described as regulators of the abiotic stress response in plant species, emerging as potential candidates for improvement of stress tolerance in plants. PpSAP1 was highly expressed in leaves and dormant buds, being down-regulated before bud dormancy release. PpSAP1 expression was moderately induced by water stresses and heat in buds. In addition, it was found that PpSAP1 strongly interacts with polyubiquitin proteins in the yeast two-hybrid system. The overexpression of PpSAP1 in transgenic plum plants led to alterations in leaf shape and an increase of water retention under drought stress. Moreover, we established that leaf morphological alterations were concomitant with a reduced cell size and down-regulation of genes involved in cell growth, such as GROWTH-REGULATING FACTOR (GRF)1-like, TONOPLAST INTRINSIC PROTEIN (TIP)-like, and TARGET OF RAPAMYCIN (TOR)-like. Especially, the inverse expression pattern of PpSAP1 and TOR-like in transgenic plum and peach buds suggests a role of PpSAP1 in cell expansion through the regulation of TOR pathway. Nature Publishing Group UK 2017-03-23 /pmc/articles/PMC5428470/ /pubmed/28336950 http://dx.doi.org/10.1038/s41598-017-00471-7 Text en © The Author(s) 2017 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 Lloret, Alba Conejero, Ana Leida, Carmen Petri, César Gil-Muñoz, Francisco Burgos, Lorenzo Badenes, María Luisa Ríos, Gabino Dual regulation of water retention and cell growth by a stress-associated protein (SAP) gene in Prunus |
title | Dual regulation of water retention and cell growth by a stress-associated protein (SAP) gene in Prunus |
title_full | Dual regulation of water retention and cell growth by a stress-associated protein (SAP) gene in Prunus |
title_fullStr | Dual regulation of water retention and cell growth by a stress-associated protein (SAP) gene in Prunus |
title_full_unstemmed | Dual regulation of water retention and cell growth by a stress-associated protein (SAP) gene in Prunus |
title_short | Dual regulation of water retention and cell growth by a stress-associated protein (SAP) gene in Prunus |
title_sort | dual regulation of water retention and cell growth by a stress-associated protein (sap) gene in prunus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428470/ https://www.ncbi.nlm.nih.gov/pubmed/28336950 http://dx.doi.org/10.1038/s41598-017-00471-7 |
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