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The developmental and iron nutritional pattern of PIC1 and NiCo does not support their interdependent and exclusive collaboration in chloroplast iron transport in Brassica napus

MAIN CONCLUSION: The accumulation of NiCo following the termination of the accumulation of iron in chloroplast suggests that NiCo is not solely involved in iron uptake processes of chloroplasts. ABSTRACT: Chloroplast iron (Fe) uptake is thought to be operated by a complex containing permease in chlo...

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Autores principales: Pham, Hong Diep, Pólya, Sára, Müller, Brigitta, Szenthe, Kálmán, Sági-Kazár, Máté, Bánkúti, Barbara, Bánáti, Ferenc, Sárvári, Éva, Fodor, Ferenc, Tamás, László, Philippar, Katrin, Solti, Ádám
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214486/
https://www.ncbi.nlm.nih.gov/pubmed/32297017
http://dx.doi.org/10.1007/s00425-020-03388-0
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author Pham, Hong Diep
Pólya, Sára
Müller, Brigitta
Szenthe, Kálmán
Sági-Kazár, Máté
Bánkúti, Barbara
Bánáti, Ferenc
Sárvári, Éva
Fodor, Ferenc
Tamás, László
Philippar, Katrin
Solti, Ádám
author_facet Pham, Hong Diep
Pólya, Sára
Müller, Brigitta
Szenthe, Kálmán
Sági-Kazár, Máté
Bánkúti, Barbara
Bánáti, Ferenc
Sárvári, Éva
Fodor, Ferenc
Tamás, László
Philippar, Katrin
Solti, Ádám
author_sort Pham, Hong Diep
collection PubMed
description MAIN CONCLUSION: The accumulation of NiCo following the termination of the accumulation of iron in chloroplast suggests that NiCo is not solely involved in iron uptake processes of chloroplasts. ABSTRACT: Chloroplast iron (Fe) uptake is thought to be operated by a complex containing permease in chloroplast 1 (PIC1) and nickel–cobalt transporter (NiCo) proteins, whereas the role of other Fe homeostasis-related transporters such as multiple antibiotic resistance protein 1 (MAR1) is less characterized. Although pieces of information exist on the regulation of chloroplast Fe uptake, including the effect of plant Fe homeostasis, the whole system has not been revealed in detail yet. Thus, we aimed to follow leaf development-scale changes in the chloroplast Fe uptake components PIC1, NiCo and MAR1 under deficient, optimal and supraoptimal Fe nutrition using Brassica napus as model. Fe deficiency decreased both the photosynthetic activity and the Fe content of plastids. Supraoptimal Fe nutrition caused neither Fe accumulation in chloroplasts nor any toxic effects, thus only fully saturated the need for Fe in the leaves. In parallel with the increasing Fe supply of plants and ageing of the leaves, the expression of BnPIC1 was tendentiously repressed. Though transcript and protein amount of BnNiCo tendentiously increased during leaf development, it was even markedly upregulated in ageing leaves. The relative transcript amount of BnMAR1 increased mainly in ageing leaves facing Fe deficiency. Taken together chloroplast physiology, Fe content and transcript amount data, the exclusive participation of NiCo in the chloroplast Fe uptake is not supported. Saturation of the Fe requirement of chloroplasts seems to be linked to the delay of decomposing the photosynthetic apparatus and keeping chloroplast Fe homeostasis in a rather constant status together with a supressed Fe uptake machinery. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00425-020-03388-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-72144862020-05-14 The developmental and iron nutritional pattern of PIC1 and NiCo does not support their interdependent and exclusive collaboration in chloroplast iron transport in Brassica napus Pham, Hong Diep Pólya, Sára Müller, Brigitta Szenthe, Kálmán Sági-Kazár, Máté Bánkúti, Barbara Bánáti, Ferenc Sárvári, Éva Fodor, Ferenc Tamás, László Philippar, Katrin Solti, Ádám Planta Original Article MAIN CONCLUSION: The accumulation of NiCo following the termination of the accumulation of iron in chloroplast suggests that NiCo is not solely involved in iron uptake processes of chloroplasts. ABSTRACT: Chloroplast iron (Fe) uptake is thought to be operated by a complex containing permease in chloroplast 1 (PIC1) and nickel–cobalt transporter (NiCo) proteins, whereas the role of other Fe homeostasis-related transporters such as multiple antibiotic resistance protein 1 (MAR1) is less characterized. Although pieces of information exist on the regulation of chloroplast Fe uptake, including the effect of plant Fe homeostasis, the whole system has not been revealed in detail yet. Thus, we aimed to follow leaf development-scale changes in the chloroplast Fe uptake components PIC1, NiCo and MAR1 under deficient, optimal and supraoptimal Fe nutrition using Brassica napus as model. Fe deficiency decreased both the photosynthetic activity and the Fe content of plastids. Supraoptimal Fe nutrition caused neither Fe accumulation in chloroplasts nor any toxic effects, thus only fully saturated the need for Fe in the leaves. In parallel with the increasing Fe supply of plants and ageing of the leaves, the expression of BnPIC1 was tendentiously repressed. Though transcript and protein amount of BnNiCo tendentiously increased during leaf development, it was even markedly upregulated in ageing leaves. The relative transcript amount of BnMAR1 increased mainly in ageing leaves facing Fe deficiency. Taken together chloroplast physiology, Fe content and transcript amount data, the exclusive participation of NiCo in the chloroplast Fe uptake is not supported. Saturation of the Fe requirement of chloroplasts seems to be linked to the delay of decomposing the photosynthetic apparatus and keeping chloroplast Fe homeostasis in a rather constant status together with a supressed Fe uptake machinery. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00425-020-03388-0) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-04-15 2020 /pmc/articles/PMC7214486/ /pubmed/32297017 http://dx.doi.org/10.1007/s00425-020-03388-0 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Pham, Hong Diep
Pólya, Sára
Müller, Brigitta
Szenthe, Kálmán
Sági-Kazár, Máté
Bánkúti, Barbara
Bánáti, Ferenc
Sárvári, Éva
Fodor, Ferenc
Tamás, László
Philippar, Katrin
Solti, Ádám
The developmental and iron nutritional pattern of PIC1 and NiCo does not support their interdependent and exclusive collaboration in chloroplast iron transport in Brassica napus
title The developmental and iron nutritional pattern of PIC1 and NiCo does not support their interdependent and exclusive collaboration in chloroplast iron transport in Brassica napus
title_full The developmental and iron nutritional pattern of PIC1 and NiCo does not support their interdependent and exclusive collaboration in chloroplast iron transport in Brassica napus
title_fullStr The developmental and iron nutritional pattern of PIC1 and NiCo does not support their interdependent and exclusive collaboration in chloroplast iron transport in Brassica napus
title_full_unstemmed The developmental and iron nutritional pattern of PIC1 and NiCo does not support their interdependent and exclusive collaboration in chloroplast iron transport in Brassica napus
title_short The developmental and iron nutritional pattern of PIC1 and NiCo does not support their interdependent and exclusive collaboration in chloroplast iron transport in Brassica napus
title_sort developmental and iron nutritional pattern of pic1 and nico does not support their interdependent and exclusive collaboration in chloroplast iron transport in brassica napus
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214486/
https://www.ncbi.nlm.nih.gov/pubmed/32297017
http://dx.doi.org/10.1007/s00425-020-03388-0
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