Quintana, JuliaBernal, MaríaScholle MarleenHolländer‐Czytko, HeikeNga, Nguyen T.Piotrowski, MarkusMendoza‐Cózatl, David G.Haydon, Michael J.Kraemer, Ute2024-02-062024-02-062022Quintana, J., Bernal, M. M., Scholle, M., Holländer-Czytko, H., Nguyen, N. T., Piotrowski, M., … & Krämer, U. (2021). Root‐to‐shoot iron partitioning in arabidopsis requires iron‐regulated transporter1 (irt1) protein but not its iron(ii) transport function. The Plant Journal, 109(4), 992-1013.https://hdl.handle.net/10115/29778This work was supported by Deutsche Forschungsgemeinschaft grants Kr1967/3-3 and 15-1, European Union FOOD-CT-2006-016253 and ERC-AdG LEAP EXTREME (788380) to UK, Ruhr University Bochum, European Union fellowship PIIF-GA-2008-219457 to MJH and Araid-Ibercaja-young scientist grant 2010, as well as Juan de la Cierva (MICINN) and JAE-DOC (CSIC) funding, to MB. Open Access funding enabled and organized by Projekt DEAL.IRON‐REGULATED TRANSPORTER1 (IRT1) is the root high‐affinity ferrous iron uptake system and indispensable for the completion of the life cycle of Arabidopsis thaliana without vigorous iron (Fe) supplementation. Here we provide evidence supporting a second role of IRT1 in root‐to‐shoot partitioning of Fe. We show that irt1 mutants over‐accumulate Fe in roots, most prominently in the cortex of the differentiation zone in irt1‐2, compared to the wild type. Shoots of irt1‐2 are severely Fe‐deficient according to Fe content and marker transcripts, as expected. We generated irt1‐2 lines producing IRT1 mutant variants carrying single amino‐acid substitutions of key residues in transmembrane helices IV and V, Ser206 and His232, which are required for transport activity in yeast. Root short‐term 55Fe uptake rates were uninformative concerning IRT1‐mediated transport. Overall irt1‐like concentrations of the secondary substrate Mn suggested that the transgenic Arabidopsis lines also remain incapable of IRT1‐mediated root Fe uptake. Yet, IRT1S206A partially complements rosette dwarfing and leaf chlorosis, as well as root‐to‐shoot Fe partitioning and gene expression defects of irt1‐2, all of which are fully complemented by wild‐type IRT1. Taken together, these results suggest a function for IRT1 in root‐to‐shoot Fe partitioning that does not require Fe transport activity of IRT1. Among the genes of which transcript levels are partially dependent on IRT1, we identify MYB DOMAIN PROTEIN10, MYB DOMAIN PROTEIN72 and NICOTIANAMINE SYNTHASE4 as candidates for effecting IRT1‐dependent Fe mobilization in roots. Understanding the biological functions of IRT1 will help to improve iron nutrition and the nutritional quality of agricultural crops.engAttribution-NonCommercial-NoDerivatives 4.0 Internacionalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/article10.1111/tpj.15611info:eu-repo/semantics/openAccess