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Silencing GmATG7 Leads to Accelerated Senescence and Enhanced Disease Resistance in Soybean

Autophagy plays a critical role in nutrient recycling/re-utilizing under nutrient deprivation conditions. However, the role of autophagy in soybeans has not been intensively investigated. In this study, the Autophay-related gene 7 (ATG7) gene in soybeans (referred to as GmATG7) was silenced using a...

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Autores principales: Hashimi, Said M., Huang, Min-Jun, Amini, Mohammad Q., Wang, Wen-Xu, Liu, Tian-Yao, Chen, Yu, Liao, Li-Na, Lan, Hu-Jiao, Liu, Jian-Zhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10671774/
https://www.ncbi.nlm.nih.gov/pubmed/38003698
http://dx.doi.org/10.3390/ijms242216508
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author Hashimi, Said M.
Huang, Min-Jun
Amini, Mohammad Q.
Wang, Wen-Xu
Liu, Tian-Yao
Chen, Yu
Liao, Li-Na
Lan, Hu-Jiao
Liu, Jian-Zhong
author_facet Hashimi, Said M.
Huang, Min-Jun
Amini, Mohammad Q.
Wang, Wen-Xu
Liu, Tian-Yao
Chen, Yu
Liao, Li-Na
Lan, Hu-Jiao
Liu, Jian-Zhong
author_sort Hashimi, Said M.
collection PubMed
description Autophagy plays a critical role in nutrient recycling/re-utilizing under nutrient deprivation conditions. However, the role of autophagy in soybeans has not been intensively investigated. In this study, the Autophay-related gene 7 (ATG7) gene in soybeans (referred to as GmATG7) was silenced using a virus-induced gene silencing approach mediated by Bean pod mottle virus (BPMV). Our results showed that ATG8 proteins were highly accumulated in the dark-treated leaves of the GmATG7-silenced plants relative to the vector control leaves (BPMV-0), which is indicative of an impaired autophagy pathway. Consistent with the impaired autophagy, the dark-treated GmATG7-silenced leaves displayed an accelerated senescence phenotype, which was not seen on the dark-treated BPMV-0 leaves. In addition, the accumulation levels of both H(2)O(2) and salicylic acid (SA) were significantly induced in the GmATG7-silenced plants compared with the BPMV-0 plants, indicating an activated immunity. Consistently, the GmATG7-silenced plants were more resistant against both Pseudomonas syringae pv. glycinea (Psg) and Soybean mosaic virus (SMV) compared with the BPMV-0 plants. However, the activated immunity in the GmATG7-silenced plant was not dependent upon the activation of MPK3/MPK6. Collectively, our results demonstrated that the function of GmATG7 is indispensable for autophagy in soybeans, and the activated immunity in the GmATG7-silenced plant is a result of impaired autophagy.
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spelling pubmed-106717742023-11-20 Silencing GmATG7 Leads to Accelerated Senescence and Enhanced Disease Resistance in Soybean Hashimi, Said M. Huang, Min-Jun Amini, Mohammad Q. Wang, Wen-Xu Liu, Tian-Yao Chen, Yu Liao, Li-Na Lan, Hu-Jiao Liu, Jian-Zhong Int J Mol Sci Article Autophagy plays a critical role in nutrient recycling/re-utilizing under nutrient deprivation conditions. However, the role of autophagy in soybeans has not been intensively investigated. In this study, the Autophay-related gene 7 (ATG7) gene in soybeans (referred to as GmATG7) was silenced using a virus-induced gene silencing approach mediated by Bean pod mottle virus (BPMV). Our results showed that ATG8 proteins were highly accumulated in the dark-treated leaves of the GmATG7-silenced plants relative to the vector control leaves (BPMV-0), which is indicative of an impaired autophagy pathway. Consistent with the impaired autophagy, the dark-treated GmATG7-silenced leaves displayed an accelerated senescence phenotype, which was not seen on the dark-treated BPMV-0 leaves. In addition, the accumulation levels of both H(2)O(2) and salicylic acid (SA) were significantly induced in the GmATG7-silenced plants compared with the BPMV-0 plants, indicating an activated immunity. Consistently, the GmATG7-silenced plants were more resistant against both Pseudomonas syringae pv. glycinea (Psg) and Soybean mosaic virus (SMV) compared with the BPMV-0 plants. However, the activated immunity in the GmATG7-silenced plant was not dependent upon the activation of MPK3/MPK6. Collectively, our results demonstrated that the function of GmATG7 is indispensable for autophagy in soybeans, and the activated immunity in the GmATG7-silenced plant is a result of impaired autophagy. MDPI 2023-11-20 /pmc/articles/PMC10671774/ /pubmed/38003698 http://dx.doi.org/10.3390/ijms242216508 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hashimi, Said M.
Huang, Min-Jun
Amini, Mohammad Q.
Wang, Wen-Xu
Liu, Tian-Yao
Chen, Yu
Liao, Li-Na
Lan, Hu-Jiao
Liu, Jian-Zhong
Silencing GmATG7 Leads to Accelerated Senescence and Enhanced Disease Resistance in Soybean
title Silencing GmATG7 Leads to Accelerated Senescence and Enhanced Disease Resistance in Soybean
title_full Silencing GmATG7 Leads to Accelerated Senescence and Enhanced Disease Resistance in Soybean
title_fullStr Silencing GmATG7 Leads to Accelerated Senescence and Enhanced Disease Resistance in Soybean
title_full_unstemmed Silencing GmATG7 Leads to Accelerated Senescence and Enhanced Disease Resistance in Soybean
title_short Silencing GmATG7 Leads to Accelerated Senescence and Enhanced Disease Resistance in Soybean
title_sort silencing gmatg7 leads to accelerated senescence and enhanced disease resistance in soybean
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10671774/
https://www.ncbi.nlm.nih.gov/pubmed/38003698
http://dx.doi.org/10.3390/ijms242216508
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