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Arabidopsis IRT2 cooperates with the high-affinity iron uptake system to maintain iron homeostasis in root epidermal cells

Authors :
Jean-François Briat
Catherine Curie
Enric Zelazny
Grégory Vert
Marie Barberon
Mathilde Séguéla
Biochimie et Physiologie Moléculaire des Plantes (BPMP)
Université de Montpellier (UM)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro)-Institut National de la Recherche Agronomique (INRA)-Centre National de la Recherche Scientifique (CNRS)
Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut National de la Recherche Agronomique (INRA)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro)
Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)
Source :
Planta, Planta, Springer Verlag, 2009, 229 (6), pp.1171-9. ⟨10.1007/s00425-009-0904-8⟩
Publication Year :
2009
Publisher :
HAL CCSD, 2009.

Abstract

International audience; Iron is an essential nutrient for all organisms but toxic when present in excess. Consequently, plants carefully regulate their iron uptake, dependent on the FRO2 ferric reductase and the IRT1 transporter, to control its homeostasis. Arabidopsis IRT2 gene, whose expression is induced in root epidermis upon iron deprivation, was shown to encode a functional iron/zinc transporter in yeast, and proposed to function in iron acquisition from the soil. In this study, we demonstrate that, unlike its close homolog IRT1, IRT2 is not involved in iron absorption from the soil since overexpression of IRT2 does not rescue the iron uptake defect of irt1-1 mutant and since a null irt2 mutant shows no chlorosis in low iron. Consistently, an IRT2-green fluorescent fusion protein, transiently expressed in culture cells, localizes to intracellular vesicles. However, IRT2 appears strictly co-regulated with FRO2 and IRT1, supporting the view that IRT2 is an integral component of the root response to iron deficiency in root epidermal cells. We propose a model where IRT2 likely prevents toxicity from IRT1-dependent iron fluxes in epidermal cells, through compartmentalization.

Details

Language :
English
ISSN :
00320935 and 14322048
Database :
OpenAIRE
Journal :
Planta, Planta, Springer Verlag, 2009, 229 (6), pp.1171-9. ⟨10.1007/s00425-009-0904-8⟩
Accession number :
edsair.doi.dedup.....2b163f14cc9cbf5d9cc56a96e306ea90
Full Text :
https://doi.org/10.1007/s00425-009-0904-8⟩