The Metacaspase TaMCA-Id Negatively Regulates Salt-Induced Programmed Cell Death and Functionally Links With Autophagy in Wheat
Metacaspases (MCAs), a family of caspase-like proteins, are important regulators of programmed cell death (PCD) in plant defense response. Autophagy is an important regulator of PCD. This study explored the underlying mechanism of the interaction among PCD, MCAs, and autophagy and their impact on wh...
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2022-06-01
|
Series: | Frontiers in Plant Science |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fpls.2022.904933/full |
_version_ | 1811241833658843136 |
---|---|
author | Jie-yu Yue Ying-jie Wang Jin-lan Jiao Wen-wen Wang Hua-zhong Wang |
author_facet | Jie-yu Yue Ying-jie Wang Jin-lan Jiao Wen-wen Wang Hua-zhong Wang |
author_sort | Jie-yu Yue |
collection | DOAJ |
description | Metacaspases (MCAs), a family of caspase-like proteins, are important regulators of programmed cell death (PCD) in plant defense response. Autophagy is an important regulator of PCD. This study explored the underlying mechanism of the interaction among PCD, MCAs, and autophagy and their impact on wheat response to salt stress. In this study, the wheat salt-responsive gene TaMCA-Id was identified. The open reading frame (ORF) of TaMCA-Id was 1,071 bp, coding 356 amino acids. The predicted molecular weight and isoelectric point were 38,337.03 Da and 8.45, respectively. TaMCA-Id had classic characteristics of type I MCAs domains, a typical N-terminal pro-domain rich in proline. TaMCA-Id was mainly localized in the chloroplast and exhibited nucleocytoplasmictrafficking under NaCl treatment. Increased expression of TaMCA-Id in wheat seedling roots and leaves was triggered by 150 mM NaCl treatment. Silencing of TaMCA-Id enhanced sensitivity of wheat seedlings to NaCl stress. Under NaCl stress, TaMCA-Id-silenced seedlings exhibited a reduction in activities of superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT), higher accumulation of H2O2 and O2.−, more serious injury to photosystem II (PSII), increase in PCD level, and autophagy activity in leaves of wheat seedlings. These results indicated that TaMCA-Id functioned in PCD through interacting with autophagy under NaCl stress, which could be used to improve the salt tolerance of crop plants. |
first_indexed | 2024-04-12T13:42:01Z |
format | Article |
id | doaj.art-7a94969521e44b0d835e68316b346cc9 |
institution | Directory Open Access Journal |
issn | 1664-462X |
language | English |
last_indexed | 2024-04-12T13:42:01Z |
publishDate | 2022-06-01 |
publisher | Frontiers Media S.A. |
record_format | Article |
series | Frontiers in Plant Science |
spelling | doaj.art-7a94969521e44b0d835e68316b346cc92022-12-22T03:30:49ZengFrontiers Media S.A.Frontiers in Plant Science1664-462X2022-06-011310.3389/fpls.2022.904933904933The Metacaspase TaMCA-Id Negatively Regulates Salt-Induced Programmed Cell Death and Functionally Links With Autophagy in WheatJie-yu YueYing-jie WangJin-lan JiaoWen-wen WangHua-zhong WangMetacaspases (MCAs), a family of caspase-like proteins, are important regulators of programmed cell death (PCD) in plant defense response. Autophagy is an important regulator of PCD. This study explored the underlying mechanism of the interaction among PCD, MCAs, and autophagy and their impact on wheat response to salt stress. In this study, the wheat salt-responsive gene TaMCA-Id was identified. The open reading frame (ORF) of TaMCA-Id was 1,071 bp, coding 356 amino acids. The predicted molecular weight and isoelectric point were 38,337.03 Da and 8.45, respectively. TaMCA-Id had classic characteristics of type I MCAs domains, a typical N-terminal pro-domain rich in proline. TaMCA-Id was mainly localized in the chloroplast and exhibited nucleocytoplasmictrafficking under NaCl treatment. Increased expression of TaMCA-Id in wheat seedling roots and leaves was triggered by 150 mM NaCl treatment. Silencing of TaMCA-Id enhanced sensitivity of wheat seedlings to NaCl stress. Under NaCl stress, TaMCA-Id-silenced seedlings exhibited a reduction in activities of superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT), higher accumulation of H2O2 and O2.−, more serious injury to photosystem II (PSII), increase in PCD level, and autophagy activity in leaves of wheat seedlings. These results indicated that TaMCA-Id functioned in PCD through interacting with autophagy under NaCl stress, which could be used to improve the salt tolerance of crop plants.https://www.frontiersin.org/articles/10.3389/fpls.2022.904933/fullautophagymetacaspaseNaCl stressPCDTaMCA1wheat seedling |
spellingShingle | Jie-yu Yue Ying-jie Wang Jin-lan Jiao Wen-wen Wang Hua-zhong Wang The Metacaspase TaMCA-Id Negatively Regulates Salt-Induced Programmed Cell Death and Functionally Links With Autophagy in Wheat Frontiers in Plant Science autophagy metacaspase NaCl stress PCD TaMCA1 wheat seedling |
title | The Metacaspase TaMCA-Id Negatively Regulates Salt-Induced Programmed Cell Death and Functionally Links With Autophagy in Wheat |
title_full | The Metacaspase TaMCA-Id Negatively Regulates Salt-Induced Programmed Cell Death and Functionally Links With Autophagy in Wheat |
title_fullStr | The Metacaspase TaMCA-Id Negatively Regulates Salt-Induced Programmed Cell Death and Functionally Links With Autophagy in Wheat |
title_full_unstemmed | The Metacaspase TaMCA-Id Negatively Regulates Salt-Induced Programmed Cell Death and Functionally Links With Autophagy in Wheat |
title_short | The Metacaspase TaMCA-Id Negatively Regulates Salt-Induced Programmed Cell Death and Functionally Links With Autophagy in Wheat |
title_sort | metacaspase tamca id negatively regulates salt induced programmed cell death and functionally links with autophagy in wheat |
topic | autophagy metacaspase NaCl stress PCD TaMCA1 wheat seedling |
url | https://www.frontiersin.org/articles/10.3389/fpls.2022.904933/full |
work_keys_str_mv | AT jieyuyue themetacaspasetamcaidnegativelyregulatessaltinducedprogrammedcelldeathandfunctionallylinkswithautophagyinwheat AT yingjiewang themetacaspasetamcaidnegativelyregulatessaltinducedprogrammedcelldeathandfunctionallylinkswithautophagyinwheat AT jinlanjiao themetacaspasetamcaidnegativelyregulatessaltinducedprogrammedcelldeathandfunctionallylinkswithautophagyinwheat AT wenwenwang themetacaspasetamcaidnegativelyregulatessaltinducedprogrammedcelldeathandfunctionallylinkswithautophagyinwheat AT huazhongwang themetacaspasetamcaidnegativelyregulatessaltinducedprogrammedcelldeathandfunctionallylinkswithautophagyinwheat AT jieyuyue metacaspasetamcaidnegativelyregulatessaltinducedprogrammedcelldeathandfunctionallylinkswithautophagyinwheat AT yingjiewang metacaspasetamcaidnegativelyregulatessaltinducedprogrammedcelldeathandfunctionallylinkswithautophagyinwheat AT jinlanjiao metacaspasetamcaidnegativelyregulatessaltinducedprogrammedcelldeathandfunctionallylinkswithautophagyinwheat AT wenwenwang metacaspasetamcaidnegativelyregulatessaltinducedprogrammedcelldeathandfunctionallylinkswithautophagyinwheat AT huazhongwang metacaspasetamcaidnegativelyregulatessaltinducedprogrammedcelldeathandfunctionallylinkswithautophagyinwheat |