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Phloem iron remodels root development in response to ammonium as the major nitrogen source

Plants use nitrate and ammonium as major nitrogen (N) sources, each affecting root development through different mechanisms. However, the exact signaling pathways involved in root development are poorly understood. Here, we show that, in Arabidopsis thaliana, either disruption of the cell wall-local...

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Autores principales: Liu, Xing Xing, Zhang, Hai Hua, Zhu, Qing Yang, Ye, Jia Yuan, Zhu, Ya Xin, Jing, Xiang Ting, Du, Wen Xin, Zhou, Miao, Lin, Xian Yong, Zheng, Shao Jian, Jin, Chong Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8799741/
https://www.ncbi.nlm.nih.gov/pubmed/35091578
http://dx.doi.org/10.1038/s41467-022-28261-4
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author Liu, Xing Xing
Zhang, Hai Hua
Zhu, Qing Yang
Ye, Jia Yuan
Zhu, Ya Xin
Jing, Xiang Ting
Du, Wen Xin
Zhou, Miao
Lin, Xian Yong
Zheng, Shao Jian
Jin, Chong Wei
author_facet Liu, Xing Xing
Zhang, Hai Hua
Zhu, Qing Yang
Ye, Jia Yuan
Zhu, Ya Xin
Jing, Xiang Ting
Du, Wen Xin
Zhou, Miao
Lin, Xian Yong
Zheng, Shao Jian
Jin, Chong Wei
author_sort Liu, Xing Xing
collection PubMed
description Plants use nitrate and ammonium as major nitrogen (N) sources, each affecting root development through different mechanisms. However, the exact signaling pathways involved in root development are poorly understood. Here, we show that, in Arabidopsis thaliana, either disruption of the cell wall-localized ferroxidase LPR2 or a decrease in iron supplementation efficiently alleviates the growth inhibition of primary roots in response to NH(4)(+) as the N source. Further study revealed that, compared with nitrate, ammonium led to excess iron accumulation in the apoplast of phloem in an LPR2-dependent manner. Such an aberrant iron accumulation subsequently causes massive callose deposition in the phloem from a resulting burst of reactive oxygen species, which impairs the function of the phloem. Therefore, ammonium attenuates primary root development by insufficiently allocating sucrose to the growth zone. Our results link phloem iron to root morphology in response to environmental cues.
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spelling pubmed-87997412022-02-07 Phloem iron remodels root development in response to ammonium as the major nitrogen source Liu, Xing Xing Zhang, Hai Hua Zhu, Qing Yang Ye, Jia Yuan Zhu, Ya Xin Jing, Xiang Ting Du, Wen Xin Zhou, Miao Lin, Xian Yong Zheng, Shao Jian Jin, Chong Wei Nat Commun Article Plants use nitrate and ammonium as major nitrogen (N) sources, each affecting root development through different mechanisms. However, the exact signaling pathways involved in root development are poorly understood. Here, we show that, in Arabidopsis thaliana, either disruption of the cell wall-localized ferroxidase LPR2 or a decrease in iron supplementation efficiently alleviates the growth inhibition of primary roots in response to NH(4)(+) as the N source. Further study revealed that, compared with nitrate, ammonium led to excess iron accumulation in the apoplast of phloem in an LPR2-dependent manner. Such an aberrant iron accumulation subsequently causes massive callose deposition in the phloem from a resulting burst of reactive oxygen species, which impairs the function of the phloem. Therefore, ammonium attenuates primary root development by insufficiently allocating sucrose to the growth zone. Our results link phloem iron to root morphology in response to environmental cues. Nature Publishing Group UK 2022-01-28 /pmc/articles/PMC8799741/ /pubmed/35091578 http://dx.doi.org/10.1038/s41467-022-28261-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Liu, Xing Xing
Zhang, Hai Hua
Zhu, Qing Yang
Ye, Jia Yuan
Zhu, Ya Xin
Jing, Xiang Ting
Du, Wen Xin
Zhou, Miao
Lin, Xian Yong
Zheng, Shao Jian
Jin, Chong Wei
Phloem iron remodels root development in response to ammonium as the major nitrogen source
title Phloem iron remodels root development in response to ammonium as the major nitrogen source
title_full Phloem iron remodels root development in response to ammonium as the major nitrogen source
title_fullStr Phloem iron remodels root development in response to ammonium as the major nitrogen source
title_full_unstemmed Phloem iron remodels root development in response to ammonium as the major nitrogen source
title_short Phloem iron remodels root development in response to ammonium as the major nitrogen source
title_sort phloem iron remodels root development in response to ammonium as the major nitrogen source
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8799741/
https://www.ncbi.nlm.nih.gov/pubmed/35091578
http://dx.doi.org/10.1038/s41467-022-28261-4
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