The Rhizophagus irregularis permease RiFTR1 functions without a ferroxidase partner for reductive iron transport

The contribution of arbuscular mycorrhizal fungi (AM fungi) to plant iron (Fe) acquisition has been demonstrated in several studies. A previous investigation revealed that the AM fungus Rhizophagus irregularis utilizes a high-affinity reductive pathway for Fe uptake, mediated by the Fe transporter RiFTR1. In this study, we used a genome-wide approach in R. irregularis to find genes encoding ferroxidases of the multicopper oxidase (MCO) gene family in an attempt to identify the ferroxidase partner of RiFTR1. Nine genes putatively encoding MCOs (RiMCO1-9) were identified. Yeast complementation assays demonstrated that RiMCO1 and RiMCO3 can function as ferroxidases, suggesting their involvement in the reductive Fe uptake pathway. Surprisingly, RiFTR1 was capable of transporting Fe in yeast without a ferroxidase partner, resembling the Fe transport mechanism of plant IRT1-like systems. RiFTR1 exhibited increase expression in arbuscules. Overexpression of RiFTR1 in Medicago truncatula roots led to enhanced mycorrhizal colonization and arbuscule abundance, highlighting the significance of Fe for AM symbiosis.

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Publication Details

Journal
Scientific Reports
Published
2025-02-18
DOI
https://doi.org/10.1038/s41598-025-88416-3
Citations
1
Primary Topic
Mycorrhizal Fungi and Plant Interactions
Type
article
Field-Weighted Citation Impact
1.75

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article

The Rhizophagus irregularis permease RiFTR1 functions without a ferroxidase partner for reductive iron transport

J. Philipp Benz, Chan Sup Shim, Araceli G. Castillo, Víctor Manuel López-Lorca et al.
1 citations
Scientific Reports
Mycorrhizal Fungi and Plant Interactions
1.75
article

The Rhizophagus irregularis permease RiFTR1 functions without a ferroxidase partner for reductive iron transport

J. Philipp Benz, Chan Sup Shim, Araceli G. Castillo, Víctor Manuel López-Lorca, Olga López-Castillo, Natalia Requena, Nuria Ferrol, Elisabeth Tamayo
article en
1 citations

Abstract

The contribution of arbuscular mycorrhizal fungi (AM fungi) to plant iron (Fe) acquisition has been demonstrated in several studies. A previous investigation revealed that the AM fungus Rhizophagus irregularis utilizes a high-affinity reductive pathway for Fe uptake, mediated by the Fe transporter RiFTR1. In this study, we used a genome-wide approach in R. irregularis to find genes encoding ferroxidases of the multicopper oxidase (MCO) gene family in an attempt to identify the ferroxidase partner of RiFTR1. Nine genes putatively encoding MCOs (RiMCO1-9) were identified. Yeast complementation assays demonstrated that RiMCO1 and RiMCO3 can function as ferroxidases, suggesting their involvement in the reductive Fe uptake pathway. Surprisingly, RiFTR1 was capable of transporting Fe in yeast without a ferroxidase partner, resembling the Fe transport mechanism of plant IRT1-like systems. RiFTR1 exhibited increase expression in arbuscules. Overexpression of RiFTR1 in Medicago truncatula roots led to enhanced mycorrhizal colonization and arbuscule abundance, highlighting the significance of Fe for AM symbiosis.

Scientific ReportsVol. 15(1)
Karlsruhe Institute of Technology (DE), Biochemical Society (GB), Estación Experimental del Zaidín (ES), Instituto de Hortofruticultura Subtropical y Mediterránea "La Mayora" (ES), University College London (GB), Technical University of Munich (DE), Universidad de Málaga (ES)
University of Pennsylvania, University of Wisconsin-Madison, European Commission, Technische Universität München, European Regional Development Fund, Agencia Estatal de Investigación
Openalex Percentile: Top 17%
Mycorrhizal Fungi and Plant Interactions
1.75
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