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AtDsPTP1 acts as a negative regulator in osmotic stress signalling during Arabidopsis seed germination and seedling establishment

Dual-specificity protein phosphatases (DsPTPs) target both tyrosine and serine/threonine residues and play roles in plant growth and development. We have characterized an Arabidopsis mutant, dsptp1, which shows a higher seed germination rate and better root elongation under osmotic stress than the w...

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Autores principales: Liu, Rui, Liu, Yinggao, Ye, Nenghui, Zhu, Guohui, Chen, Moxian, Jia, Liguo, Xia, Yiji, Shi, Lu, Jia, Wensuo, Zhang, Jianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339596/
https://www.ncbi.nlm.nih.gov/pubmed/25540435
http://dx.doi.org/10.1093/jxb/eru484
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author Liu, Rui
Liu, Yinggao
Ye, Nenghui
Zhu, Guohui
Chen, Moxian
Jia, Liguo
Xia, Yiji
Shi, Lu
Jia, Wensuo
Zhang, Jianhua
author_facet Liu, Rui
Liu, Yinggao
Ye, Nenghui
Zhu, Guohui
Chen, Moxian
Jia, Liguo
Xia, Yiji
Shi, Lu
Jia, Wensuo
Zhang, Jianhua
author_sort Liu, Rui
collection PubMed
description Dual-specificity protein phosphatases (DsPTPs) target both tyrosine and serine/threonine residues and play roles in plant growth and development. We have characterized an Arabidopsis mutant, dsptp1, which shows a higher seed germination rate and better root elongation under osmotic stress than the wild type. By contrast, its overexpression line, DsPTP1-OE, shows inhibited seed germination and root elongation; and its complemented line, DsPTP1-Com, resembles the wild type and rescues DsPTP1-OE under osmotic stress. Expression of AtDsPTP1 is enhanced by osmotic stress in seed coats, bases of rosette leaves, and roots. Compared with the wild type, the dsptp1 mutant shows increased proline accumulation, reduced malondialdehyde (MDA) content and ion leakage, and enhanced antioxidant enzyme activity in response to osmotic stress. AtDsPTP1 regulates the transcript levels of various dehydration-responsive genes under osmotic stress. Abscisic acid (ABA) accumulation in dsptp1 under osmotic stress is reduced with reduced expression of the ABA-biosynthesis gene NCED3 and increased expression of the ABA-catabolism gene CYP707A4. AtDsPTP1 also regulates the expression of key components in the ABA-signalling pathway. In conclusion, AtDsPTP1 regulates ABA accumulation, and acts as a negative regulator in osmotic stress signalling during Arabidospsis seed germination and seedling establishment.
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spelling pubmed-43395962015-03-18 AtDsPTP1 acts as a negative regulator in osmotic stress signalling during Arabidopsis seed germination and seedling establishment Liu, Rui Liu, Yinggao Ye, Nenghui Zhu, Guohui Chen, Moxian Jia, Liguo Xia, Yiji Shi, Lu Jia, Wensuo Zhang, Jianhua J Exp Bot Research Paper Dual-specificity protein phosphatases (DsPTPs) target both tyrosine and serine/threonine residues and play roles in plant growth and development. We have characterized an Arabidopsis mutant, dsptp1, which shows a higher seed germination rate and better root elongation under osmotic stress than the wild type. By contrast, its overexpression line, DsPTP1-OE, shows inhibited seed germination and root elongation; and its complemented line, DsPTP1-Com, resembles the wild type and rescues DsPTP1-OE under osmotic stress. Expression of AtDsPTP1 is enhanced by osmotic stress in seed coats, bases of rosette leaves, and roots. Compared with the wild type, the dsptp1 mutant shows increased proline accumulation, reduced malondialdehyde (MDA) content and ion leakage, and enhanced antioxidant enzyme activity in response to osmotic stress. AtDsPTP1 regulates the transcript levels of various dehydration-responsive genes under osmotic stress. Abscisic acid (ABA) accumulation in dsptp1 under osmotic stress is reduced with reduced expression of the ABA-biosynthesis gene NCED3 and increased expression of the ABA-catabolism gene CYP707A4. AtDsPTP1 also regulates the expression of key components in the ABA-signalling pathway. In conclusion, AtDsPTP1 regulates ABA accumulation, and acts as a negative regulator in osmotic stress signalling during Arabidospsis seed germination and seedling establishment. Oxford University Press 2015-03 2014-12-24 /pmc/articles/PMC4339596/ /pubmed/25540435 http://dx.doi.org/10.1093/jxb/eru484 Text en © The Author 2014. 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
Liu, Rui
Liu, Yinggao
Ye, Nenghui
Zhu, Guohui
Chen, Moxian
Jia, Liguo
Xia, Yiji
Shi, Lu
Jia, Wensuo
Zhang, Jianhua
AtDsPTP1 acts as a negative regulator in osmotic stress signalling during Arabidopsis seed germination and seedling establishment
title AtDsPTP1 acts as a negative regulator in osmotic stress signalling during Arabidopsis seed germination and seedling establishment
title_full AtDsPTP1 acts as a negative regulator in osmotic stress signalling during Arabidopsis seed germination and seedling establishment
title_fullStr AtDsPTP1 acts as a negative regulator in osmotic stress signalling during Arabidopsis seed germination and seedling establishment
title_full_unstemmed AtDsPTP1 acts as a negative regulator in osmotic stress signalling during Arabidopsis seed germination and seedling establishment
title_short AtDsPTP1 acts as a negative regulator in osmotic stress signalling during Arabidopsis seed germination and seedling establishment
title_sort atdsptp1 acts as a negative regulator in osmotic stress signalling during arabidopsis seed germination and seedling establishment
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339596/
https://www.ncbi.nlm.nih.gov/pubmed/25540435
http://dx.doi.org/10.1093/jxb/eru484
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