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Deregulated High Affinity Copper Transport Alters Iron Homeostasis in Arabidopsis

The present work describes the effects on iron homeostasis when copper transport was deregulated in Arabidopsis thaliana by overexpressing high affinity copper transporters COPT1 and COPT3 (COPT(OE)). A genome-wide analysis conducted on COPT1(OE) plants, highlighted that iron homeostasis gene expres...

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Autores principales: Perea-García, Ana, Andrés-Bordería, Amparo, Vera-Sirera, Francisco, Pérez-Amador, Miguel Angel, Puig, Sergi, Peñarrubia, Lola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7390907/
https://www.ncbi.nlm.nih.gov/pubmed/32793263
http://dx.doi.org/10.3389/fpls.2020.01106
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author Perea-García, Ana
Andrés-Bordería, Amparo
Vera-Sirera, Francisco
Pérez-Amador, Miguel Angel
Puig, Sergi
Peñarrubia, Lola
author_facet Perea-García, Ana
Andrés-Bordería, Amparo
Vera-Sirera, Francisco
Pérez-Amador, Miguel Angel
Puig, Sergi
Peñarrubia, Lola
author_sort Perea-García, Ana
collection PubMed
description The present work describes the effects on iron homeostasis when copper transport was deregulated in Arabidopsis thaliana by overexpressing high affinity copper transporters COPT1 and COPT3 (COPT(OE)). A genome-wide analysis conducted on COPT1(OE) plants, highlighted that iron homeostasis gene expression was affected under both copper deficiency and excess. Among the altered genes were those encoding the iron uptake machinery and their transcriptional regulators. Subsequently, COPT(OE) seedlings contained less iron and were more sensitive than controls to iron deficiency. The deregulation of copper (I) uptake hindered the transcriptional activation of the subgroup Ib of basic helix-loop-helix (bHLH-Ib) factors under copper deficiency. Oppositely, copper excess inhibited the expression of the master regulator FIT but activated bHLH-Ib expression in COPT(OE) plants, in both cases leading to the lack of an adequate iron uptake response. As copper increased in the media, iron (III) was accumulated in roots, and the ratio iron (III)/iron (II) was increased in COPT(OE) plants. Thus, iron (III) overloading in COPT(OE) roots inhibited local iron deficiency responses, aimed to metal uptake from soil, leading to a general lower iron content in the COPT(OE) seedlings. These results emphasized the importance of appropriate spatiotemporal copper uptake for iron homeostasis under non-optimal copper supply. The understanding of the role of copper uptake in iron metabolism could be applied for increasing crops resistance to iron deficiency.
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spelling pubmed-73909072020-08-12 Deregulated High Affinity Copper Transport Alters Iron Homeostasis in Arabidopsis Perea-García, Ana Andrés-Bordería, Amparo Vera-Sirera, Francisco Pérez-Amador, Miguel Angel Puig, Sergi Peñarrubia, Lola Front Plant Sci Plant Science The present work describes the effects on iron homeostasis when copper transport was deregulated in Arabidopsis thaliana by overexpressing high affinity copper transporters COPT1 and COPT3 (COPT(OE)). A genome-wide analysis conducted on COPT1(OE) plants, highlighted that iron homeostasis gene expression was affected under both copper deficiency and excess. Among the altered genes were those encoding the iron uptake machinery and their transcriptional regulators. Subsequently, COPT(OE) seedlings contained less iron and were more sensitive than controls to iron deficiency. The deregulation of copper (I) uptake hindered the transcriptional activation of the subgroup Ib of basic helix-loop-helix (bHLH-Ib) factors under copper deficiency. Oppositely, copper excess inhibited the expression of the master regulator FIT but activated bHLH-Ib expression in COPT(OE) plants, in both cases leading to the lack of an adequate iron uptake response. As copper increased in the media, iron (III) was accumulated in roots, and the ratio iron (III)/iron (II) was increased in COPT(OE) plants. Thus, iron (III) overloading in COPT(OE) roots inhibited local iron deficiency responses, aimed to metal uptake from soil, leading to a general lower iron content in the COPT(OE) seedlings. These results emphasized the importance of appropriate spatiotemporal copper uptake for iron homeostasis under non-optimal copper supply. The understanding of the role of copper uptake in iron metabolism could be applied for increasing crops resistance to iron deficiency. Frontiers Media S.A. 2020-07-23 /pmc/articles/PMC7390907/ /pubmed/32793263 http://dx.doi.org/10.3389/fpls.2020.01106 Text en Copyright © 2020 Perea-García, Andrés-Bordería, Vera-Sirera, Pérez-Amador, Puig and Peñarrubia http://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
Perea-García, Ana
Andrés-Bordería, Amparo
Vera-Sirera, Francisco
Pérez-Amador, Miguel Angel
Puig, Sergi
Peñarrubia, Lola
Deregulated High Affinity Copper Transport Alters Iron Homeostasis in Arabidopsis
title Deregulated High Affinity Copper Transport Alters Iron Homeostasis in Arabidopsis
title_full Deregulated High Affinity Copper Transport Alters Iron Homeostasis in Arabidopsis
title_fullStr Deregulated High Affinity Copper Transport Alters Iron Homeostasis in Arabidopsis
title_full_unstemmed Deregulated High Affinity Copper Transport Alters Iron Homeostasis in Arabidopsis
title_short Deregulated High Affinity Copper Transport Alters Iron Homeostasis in Arabidopsis
title_sort deregulated high affinity copper transport alters iron homeostasis in arabidopsis
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7390907/
https://www.ncbi.nlm.nih.gov/pubmed/32793263
http://dx.doi.org/10.3389/fpls.2020.01106
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