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Protease inhibitor ASP enhances freezing tolerance by inhibiting protein degradation in kumquat

Cold acclimation is a complex biological process leading to the development of freezing tolerance in plants. In this study, we demonstrated that cold-induced expression of protease inhibitor FmASP in a Citrus-relative species kumquat [Fortunella margarita (Lour.) Swingle] contributes to its freezing...

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Autores principales: Yang, Hua, Qiao, Ke-wei, Teng, Jin-jing, Chen, Jia-bei, Zhong, Ying-li, Rao, Li-qun, Xiong, Xing-yao, Li, Huang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541525/
https://www.ncbi.nlm.nih.gov/pubmed/37786860
http://dx.doi.org/10.1093/hr/uhad023
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author Yang, Hua
Qiao, Ke-wei
Teng, Jin-jing
Chen, Jia-bei
Zhong, Ying-li
Rao, Li-qun
Xiong, Xing-yao
Li, Huang
author_facet Yang, Hua
Qiao, Ke-wei
Teng, Jin-jing
Chen, Jia-bei
Zhong, Ying-li
Rao, Li-qun
Xiong, Xing-yao
Li, Huang
author_sort Yang, Hua
collection PubMed
description Cold acclimation is a complex biological process leading to the development of freezing tolerance in plants. In this study, we demonstrated that cold-induced expression of protease inhibitor FmASP in a Citrus-relative species kumquat [Fortunella margarita (Lour.) Swingle] contributes to its freezing tolerance by minimizing protein degradation. Firstly, we found that only cold-acclimated kumquat plants, despite extensive leaf cellular damage during freezing, were able to resume their normal growth upon stress relief. To dissect the impact of cold acclimation on this anti-freezing performance, we conducted protein abundance assays and quantitative proteomic analysis of kumquat leaves subjected to cold acclimation (4°C), freezing treatment (−10°C) and post-freezing recovery (25°C). FmASP (Against Serine Protease) and several non-specific proteases were identified as differentially expressed proteins induced by cold acclimation and associated with stable protein abundance throughout the course of low-temperature treatment. FmASP was further characterized as a robust inhibitor of multiple proteases. In addition, heterogeneous expression of FmASP in Arabidopsis confirmed its positive role in freezing tolerance. Finally, we proposed a working model of FmASP and illustrated how this extracellular-localized protease inhibitor protects proteins from degradation, thereby maintaining essential cellular function for post-freezing recovery. These findings revealed the important role of protease inhibition in freezing response and provide insights on how this role may help develop new strategies to enhance plant freezing tolerance.
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spelling pubmed-105415252023-10-02 Protease inhibitor ASP enhances freezing tolerance by inhibiting protein degradation in kumquat Yang, Hua Qiao, Ke-wei Teng, Jin-jing Chen, Jia-bei Zhong, Ying-li Rao, Li-qun Xiong, Xing-yao Li, Huang Hortic Res Article Cold acclimation is a complex biological process leading to the development of freezing tolerance in plants. In this study, we demonstrated that cold-induced expression of protease inhibitor FmASP in a Citrus-relative species kumquat [Fortunella margarita (Lour.) Swingle] contributes to its freezing tolerance by minimizing protein degradation. Firstly, we found that only cold-acclimated kumquat plants, despite extensive leaf cellular damage during freezing, were able to resume their normal growth upon stress relief. To dissect the impact of cold acclimation on this anti-freezing performance, we conducted protein abundance assays and quantitative proteomic analysis of kumquat leaves subjected to cold acclimation (4°C), freezing treatment (−10°C) and post-freezing recovery (25°C). FmASP (Against Serine Protease) and several non-specific proteases were identified as differentially expressed proteins induced by cold acclimation and associated with stable protein abundance throughout the course of low-temperature treatment. FmASP was further characterized as a robust inhibitor of multiple proteases. In addition, heterogeneous expression of FmASP in Arabidopsis confirmed its positive role in freezing tolerance. Finally, we proposed a working model of FmASP and illustrated how this extracellular-localized protease inhibitor protects proteins from degradation, thereby maintaining essential cellular function for post-freezing recovery. These findings revealed the important role of protease inhibition in freezing response and provide insights on how this role may help develop new strategies to enhance plant freezing tolerance. Oxford University Press 2023-02-16 /pmc/articles/PMC10541525/ /pubmed/37786860 http://dx.doi.org/10.1093/hr/uhad023 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nanjing Agricultural University. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Yang, Hua
Qiao, Ke-wei
Teng, Jin-jing
Chen, Jia-bei
Zhong, Ying-li
Rao, Li-qun
Xiong, Xing-yao
Li, Huang
Protease inhibitor ASP enhances freezing tolerance by inhibiting protein degradation in kumquat
title Protease inhibitor ASP enhances freezing tolerance by inhibiting protein degradation in kumquat
title_full Protease inhibitor ASP enhances freezing tolerance by inhibiting protein degradation in kumquat
title_fullStr Protease inhibitor ASP enhances freezing tolerance by inhibiting protein degradation in kumquat
title_full_unstemmed Protease inhibitor ASP enhances freezing tolerance by inhibiting protein degradation in kumquat
title_short Protease inhibitor ASP enhances freezing tolerance by inhibiting protein degradation in kumquat
title_sort protease inhibitor asp enhances freezing tolerance by inhibiting protein degradation in kumquat
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541525/
https://www.ncbi.nlm.nih.gov/pubmed/37786860
http://dx.doi.org/10.1093/hr/uhad023
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