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Dynamic Changes in Reactive Oxygen Species in the Shoot Apex Contribute to Stem Cell Death in Arabidopsis thaliana

In monocarpic plants, stem cells are fated to die. However, the potential mechanism of stem cell death has remained elusive. Here, we reveal that the levels of two forms of reactive oxygen species (ROS), superoxide anion free radical ([Formula: see text]) and hydrogen peroxide (H(2)O(2)), show dynam...

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Autores principales: Wang, Yukun, Shirakawa, Makoto, Ito, Toshiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8998593/
https://www.ncbi.nlm.nih.gov/pubmed/35409227
http://dx.doi.org/10.3390/ijms23073864
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author Wang, Yukun
Shirakawa, Makoto
Ito, Toshiro
author_facet Wang, Yukun
Shirakawa, Makoto
Ito, Toshiro
author_sort Wang, Yukun
collection PubMed
description In monocarpic plants, stem cells are fated to die. However, the potential mechanism of stem cell death has remained elusive. Here, we reveal that the levels of two forms of reactive oxygen species (ROS), superoxide anion free radical ([Formula: see text]) and hydrogen peroxide (H(2)O(2)), show dynamic changes in the shoot apex during the plant life cycle of Arabidopsis thaliana. We found that the level of [Formula: see text] decreased and disappeared at four weeks after bolting (WAB), while H(2)O(2) appeared at 3 WAB and showed a burst at 5 WAB. The timing of dynamic changes in [Formula: see text] and H(2)O(2) was delayed for approximately three weeks in clv3-2, which has a longer lifespan. Moreover, exogenous application of H(2)O(2) inhibited the expression of the stem cell determinant WUSCHEL (WUS) and promoted the expression of the developmentally programmed cell death (dPCD) marker gene ORESARA 1 (ORE1). These results indicate that H(2)O(2) triggers an important signal inducing dPCD in stem cells. Given that [Formula: see text] plays roles in maintaining WUS expression and stem cell activity, we speculate that the dynamic shift from [Formula: see text] to H(2)O(2) in the shoot apex results in stem cell death. Our findings provide novel insights for understanding ROS-mediated regulation during plant stem cell death.
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spelling pubmed-89985932022-04-12 Dynamic Changes in Reactive Oxygen Species in the Shoot Apex Contribute to Stem Cell Death in Arabidopsis thaliana Wang, Yukun Shirakawa, Makoto Ito, Toshiro Int J Mol Sci Article In monocarpic plants, stem cells are fated to die. However, the potential mechanism of stem cell death has remained elusive. Here, we reveal that the levels of two forms of reactive oxygen species (ROS), superoxide anion free radical ([Formula: see text]) and hydrogen peroxide (H(2)O(2)), show dynamic changes in the shoot apex during the plant life cycle of Arabidopsis thaliana. We found that the level of [Formula: see text] decreased and disappeared at four weeks after bolting (WAB), while H(2)O(2) appeared at 3 WAB and showed a burst at 5 WAB. The timing of dynamic changes in [Formula: see text] and H(2)O(2) was delayed for approximately three weeks in clv3-2, which has a longer lifespan. Moreover, exogenous application of H(2)O(2) inhibited the expression of the stem cell determinant WUSCHEL (WUS) and promoted the expression of the developmentally programmed cell death (dPCD) marker gene ORESARA 1 (ORE1). These results indicate that H(2)O(2) triggers an important signal inducing dPCD in stem cells. Given that [Formula: see text] plays roles in maintaining WUS expression and stem cell activity, we speculate that the dynamic shift from [Formula: see text] to H(2)O(2) in the shoot apex results in stem cell death. Our findings provide novel insights for understanding ROS-mediated regulation during plant stem cell death. MDPI 2022-03-31 /pmc/articles/PMC8998593/ /pubmed/35409227 http://dx.doi.org/10.3390/ijms23073864 Text en © 2022 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
Wang, Yukun
Shirakawa, Makoto
Ito, Toshiro
Dynamic Changes in Reactive Oxygen Species in the Shoot Apex Contribute to Stem Cell Death in Arabidopsis thaliana
title Dynamic Changes in Reactive Oxygen Species in the Shoot Apex Contribute to Stem Cell Death in Arabidopsis thaliana
title_full Dynamic Changes in Reactive Oxygen Species in the Shoot Apex Contribute to Stem Cell Death in Arabidopsis thaliana
title_fullStr Dynamic Changes in Reactive Oxygen Species in the Shoot Apex Contribute to Stem Cell Death in Arabidopsis thaliana
title_full_unstemmed Dynamic Changes in Reactive Oxygen Species in the Shoot Apex Contribute to Stem Cell Death in Arabidopsis thaliana
title_short Dynamic Changes in Reactive Oxygen Species in the Shoot Apex Contribute to Stem Cell Death in Arabidopsis thaliana
title_sort dynamic changes in reactive oxygen species in the shoot apex contribute to stem cell death in arabidopsis thaliana
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8998593/
https://www.ncbi.nlm.nih.gov/pubmed/35409227
http://dx.doi.org/10.3390/ijms23073864
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