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The ferroxidases are critical for Fe(II) oxidation in xylem to ensure a healthy Fe allocation in Arabidopsis thaliana

The long-distance transport of iron (Fe) in the xylem is critical for maintaining systemic Fe homeostasis in plants. The loading form of Fe(II) into the xylem and the long-distance translocation form of Fe(III)–citrate have been identified, but how Fe(II) is oxidized to Fe(III) in the xylem remains...

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Autores principales: Zhu, Qing-Yang, Wang, Yun, Liu, Xing-Xing, Ye, Jia-Yuan, Zhou, Miao, Jing, Xiang-Ting, Du, Wen-Xin, Hu, Wei-Jie, He, Chao, Zhu, Ya-Xin, Jin, Chong-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9428407/
https://www.ncbi.nlm.nih.gov/pubmed/36061760
http://dx.doi.org/10.3389/fpls.2022.958984
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author Zhu, Qing-Yang
Wang, Yun
Liu, Xing-Xing
Ye, Jia-Yuan
Zhou, Miao
Jing, Xiang-Ting
Du, Wen-Xin
Hu, Wei-Jie
He, Chao
Zhu, Ya-Xin
Jin, Chong-Wei
author_facet Zhu, Qing-Yang
Wang, Yun
Liu, Xing-Xing
Ye, Jia-Yuan
Zhou, Miao
Jing, Xiang-Ting
Du, Wen-Xin
Hu, Wei-Jie
He, Chao
Zhu, Ya-Xin
Jin, Chong-Wei
author_sort Zhu, Qing-Yang
collection PubMed
description The long-distance transport of iron (Fe) in the xylem is critical for maintaining systemic Fe homeostasis in plants. The loading form of Fe(II) into the xylem and the long-distance translocation form of Fe(III)–citrate have been identified, but how Fe(II) is oxidized to Fe(III) in the xylem remains unknown. Here, we showed that the cell wall-resided ferroxidases LPR1 and LPR2 (LPRs) were both specifically expressed in the vascular tissues of Arabidopsis thaliana, while disruption of both of them increased Fe(II) in the xylem sap and caused excessive Fe deposition in the xylem vessel wall under Fe-sufficient conditions. As a result, a large amount of Fe accumulated in both roots and shoots, hindering plant growth. Moreover, under low-Fe conditions, LPRs were preferentially induced in old leaves, but the loss of LPRs increased Fe deposition in the vasculature of older leaves and impeded Fe allocation to younger leaves. Therefore, disruption of both LPRs resulted in severer chlorosis in young leaves under Fe-deficient conditions. Taken together, the oxidation of Fe(II) to Fe(III) by LPRs in the cell wall of vasculature plays an important role in xylem Fe allocation, ensuring healthy Fe homeostasis for normal plant growth.
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spelling pubmed-94284072022-09-01 The ferroxidases are critical for Fe(II) oxidation in xylem to ensure a healthy Fe allocation in Arabidopsis thaliana Zhu, Qing-Yang Wang, Yun Liu, Xing-Xing Ye, Jia-Yuan Zhou, Miao Jing, Xiang-Ting Du, Wen-Xin Hu, Wei-Jie He, Chao Zhu, Ya-Xin Jin, Chong-Wei Front Plant Sci Plant Science The long-distance transport of iron (Fe) in the xylem is critical for maintaining systemic Fe homeostasis in plants. The loading form of Fe(II) into the xylem and the long-distance translocation form of Fe(III)–citrate have been identified, but how Fe(II) is oxidized to Fe(III) in the xylem remains unknown. Here, we showed that the cell wall-resided ferroxidases LPR1 and LPR2 (LPRs) were both specifically expressed in the vascular tissues of Arabidopsis thaliana, while disruption of both of them increased Fe(II) in the xylem sap and caused excessive Fe deposition in the xylem vessel wall under Fe-sufficient conditions. As a result, a large amount of Fe accumulated in both roots and shoots, hindering plant growth. Moreover, under low-Fe conditions, LPRs were preferentially induced in old leaves, but the loss of LPRs increased Fe deposition in the vasculature of older leaves and impeded Fe allocation to younger leaves. Therefore, disruption of both LPRs resulted in severer chlorosis in young leaves under Fe-deficient conditions. Taken together, the oxidation of Fe(II) to Fe(III) by LPRs in the cell wall of vasculature plays an important role in xylem Fe allocation, ensuring healthy Fe homeostasis for normal plant growth. Frontiers Media S.A. 2022-08-17 /pmc/articles/PMC9428407/ /pubmed/36061760 http://dx.doi.org/10.3389/fpls.2022.958984 Text en Copyright © 2022 Zhu, Wang, Liu, Ye, Zhou, Jing, Du, Hu, He, Zhu and Jin. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Zhu, Qing-Yang
Wang, Yun
Liu, Xing-Xing
Ye, Jia-Yuan
Zhou, Miao
Jing, Xiang-Ting
Du, Wen-Xin
Hu, Wei-Jie
He, Chao
Zhu, Ya-Xin
Jin, Chong-Wei
The ferroxidases are critical for Fe(II) oxidation in xylem to ensure a healthy Fe allocation in Arabidopsis thaliana
title The ferroxidases are critical for Fe(II) oxidation in xylem to ensure a healthy Fe allocation in Arabidopsis thaliana
title_full The ferroxidases are critical for Fe(II) oxidation in xylem to ensure a healthy Fe allocation in Arabidopsis thaliana
title_fullStr The ferroxidases are critical for Fe(II) oxidation in xylem to ensure a healthy Fe allocation in Arabidopsis thaliana
title_full_unstemmed The ferroxidases are critical for Fe(II) oxidation in xylem to ensure a healthy Fe allocation in Arabidopsis thaliana
title_short The ferroxidases are critical for Fe(II) oxidation in xylem to ensure a healthy Fe allocation in Arabidopsis thaliana
title_sort ferroxidases are critical for fe(ii) oxidation in xylem to ensure a healthy fe allocation in arabidopsis thaliana
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9428407/
https://www.ncbi.nlm.nih.gov/pubmed/36061760
http://dx.doi.org/10.3389/fpls.2022.958984
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