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Transcriptome analysis reveals the mechanisms for mycorrhiza-enhanced salt tolerance in rice

More than half of the global population relies on rice as a staple food, but salinization of soil presents a great threat to rice cultivation. Although previous studies have addressed the possible benefits of arbuscular mycorrhizal (AM) symbiosis for rice under salinity stress, the underlying molecu...

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Autores principales: Hsieh, Chen, Chen, Yun-Hsin, Chang, Kai-Chieh, Yang, Shu-Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9806932/
https://www.ncbi.nlm.nih.gov/pubmed/36600910
http://dx.doi.org/10.3389/fpls.2022.1072171
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author Hsieh, Chen
Chen, Yun-Hsin
Chang, Kai-Chieh
Yang, Shu-Yi
author_facet Hsieh, Chen
Chen, Yun-Hsin
Chang, Kai-Chieh
Yang, Shu-Yi
author_sort Hsieh, Chen
collection PubMed
description More than half of the global population relies on rice as a staple food, but salinization of soil presents a great threat to rice cultivation. Although previous studies have addressed the possible benefits of arbuscular mycorrhizal (AM) symbiosis for rice under salinity stress, the underlying molecular mechanisms are still unclear. In this study, we found that mycorrhizal rice had better shoot and reproductive growth and a significantly higher K(+)/Na(+) ratio in the shoot. The reactive oxygen species (ROS) scavenging capacity in rice shoots was also improved by AM symbiosis. To elucidate the molecular mechanisms required for AM-improved salt tolerance, transcriptome analysis revealing the differentially expressed genes (DEGs) based on the response to AM symbiosis, salinity or specific tissue was performed. Thirteen percent of DEGs showed tissue-preferred responses to both AM symbiosis and salt stress and might be the key genes contributing to AM-enhanced salt tolerance. Gene Ontology (GO) enrichment analysis identified GO terms specifically appearing in this category, including cell wall, oxidoreductase activity, reproduction and ester-related terms. Interestingly, GO terms related to phosphate (Pi) homeostasis were also found, suggesting the possible role of the Pi-related signaling pathway involved in AM-enhanced salt tolerance. Intriguingly, under nonsaline conditions, AM symbiosis influenced the expression of these genes in a similar way as salinity, especially in the shoots. Overall, our results indicate that AM symbiosis may possibly use a multipronged approach to influence gene expression in a way similar to salinity, and this modification could help plants be prepared for salt stress.
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spelling pubmed-98069322023-01-03 Transcriptome analysis reveals the mechanisms for mycorrhiza-enhanced salt tolerance in rice Hsieh, Chen Chen, Yun-Hsin Chang, Kai-Chieh Yang, Shu-Yi Front Plant Sci Plant Science More than half of the global population relies on rice as a staple food, but salinization of soil presents a great threat to rice cultivation. Although previous studies have addressed the possible benefits of arbuscular mycorrhizal (AM) symbiosis for rice under salinity stress, the underlying molecular mechanisms are still unclear. In this study, we found that mycorrhizal rice had better shoot and reproductive growth and a significantly higher K(+)/Na(+) ratio in the shoot. The reactive oxygen species (ROS) scavenging capacity in rice shoots was also improved by AM symbiosis. To elucidate the molecular mechanisms required for AM-improved salt tolerance, transcriptome analysis revealing the differentially expressed genes (DEGs) based on the response to AM symbiosis, salinity or specific tissue was performed. Thirteen percent of DEGs showed tissue-preferred responses to both AM symbiosis and salt stress and might be the key genes contributing to AM-enhanced salt tolerance. Gene Ontology (GO) enrichment analysis identified GO terms specifically appearing in this category, including cell wall, oxidoreductase activity, reproduction and ester-related terms. Interestingly, GO terms related to phosphate (Pi) homeostasis were also found, suggesting the possible role of the Pi-related signaling pathway involved in AM-enhanced salt tolerance. Intriguingly, under nonsaline conditions, AM symbiosis influenced the expression of these genes in a similar way as salinity, especially in the shoots. Overall, our results indicate that AM symbiosis may possibly use a multipronged approach to influence gene expression in a way similar to salinity, and this modification could help plants be prepared for salt stress. Frontiers Media S.A. 2022-12-19 /pmc/articles/PMC9806932/ /pubmed/36600910 http://dx.doi.org/10.3389/fpls.2022.1072171 Text en Copyright © 2022 Hsieh, Chen, Chang and Yang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Hsieh, Chen
Chen, Yun-Hsin
Chang, Kai-Chieh
Yang, Shu-Yi
Transcriptome analysis reveals the mechanisms for mycorrhiza-enhanced salt tolerance in rice
title Transcriptome analysis reveals the mechanisms for mycorrhiza-enhanced salt tolerance in rice
title_full Transcriptome analysis reveals the mechanisms for mycorrhiza-enhanced salt tolerance in rice
title_fullStr Transcriptome analysis reveals the mechanisms for mycorrhiza-enhanced salt tolerance in rice
title_full_unstemmed Transcriptome analysis reveals the mechanisms for mycorrhiza-enhanced salt tolerance in rice
title_short Transcriptome analysis reveals the mechanisms for mycorrhiza-enhanced salt tolerance in rice
title_sort transcriptome analysis reveals the mechanisms for mycorrhiza-enhanced salt tolerance in rice
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9806932/
https://www.ncbi.nlm.nih.gov/pubmed/36600910
http://dx.doi.org/10.3389/fpls.2022.1072171
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