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The SlZRT1 Gene Encodes a Plasma Membrane-Located ZIP (Zrt-, Irt-Like Protein) Transporter in the Ectomycorrhizal Fungus Suillus luteus

Authors :
Laura Coninx
Michiel Op De Beeck
Eli Slenders
Joske Ruytinx
Jan V. Colpaert
Emmanuelle Morin
Natascha Arnauts
Annegret Kohler
Anneleen Thoonen
Plant Genetics
Microbiology
Department of Bio-engineering Sciences
Hasselt University
Interactions Arbres-Microorganismes (IAM)
Université de Lorraine (UL)-Institut National de la Recherche Agronomique (INRA)
Hasselt University (UHasselt)
Institut National de la Recherche Agronomique (INRA)-Université de Lorraine (UL)
Source :
Frontiers in Microbiology (8), 2320. (2017), Frontiers in Microbiology, Frontiers in Microbiology, Frontiers Media, 2017, 8, pp.2320. ⟨10.3389/fmicb.2017.02320⟩, Frontiers in Microbiology, Vol 8 (2017)
Publication Year :
2017

Abstract

Zinc (Zn) is an essential micronutrient but may become toxic when present in excess. In Zn-contaminated environments, trees can be protected from Zn toxicity by their root-associated micro-organisms, in particular ectomycorrhizal fungi. The mechanisms of cellular Zn homeostasis in ectomycorrhizal fungi and their contribution to the host tree's Zn status are however not yet fully understood. The aim of this study was to identify and characterize transporters involved in Zn uptake in the ectomycorrhizal fungus Suillus luteus, a cosmopolitan pine mycobiont. Zn uptake in fungi is known to be predominantly governed by members of the ZIP (Zrt/IrtT-like protein) family of Zn transporters. Four ZIP transporter encoding genes were identified in the S. luteus genome. By in silico and phylogenetic analysis, one of these proteins, SlZRT1, was predicted to be a plasma membrane located Zn importer. Heterologous expression in yeast confirmed the predicted function and localization of the protein. A gene expression analysis via RT-qPCR was performed in S. luteus to establish whether SlZRT1 expression is affected by external Zn concentrations. SlZRT1 transcripts accumulated almost immediately, though transiently upon growth in the absence of Zn. Exposure to elevated concentrations of Zn resulted in a significant reduction of SlZRT1 transcripts within the first hour after initiation of the exposure. Altogether, the data support a role as cellular Zn importer for SlZRT1 and indicate a key role in cellular Zn uptake of S. luteus. Further research is needed to understand the eventual contribution of SlZRT1 to the Zn status of the host plant. This work was financially supported by the Research Foundation Flanders (FWO Project G079213N). LC holds a Flanders Innovation & Entrepreneurships Ph.D. fellowship (IWT Project 141461) and her research visit at INRA Grand Est Nancy was funded by the Laboratory of Excellence Advanced Research on the Biology of Tree and Forest Ecosystems (ARBRE; grant No. ANR-11-LABX-0002-01). Part of the computations were performed at the INRA Grand Est-Nancy Ecogenomics facilities. The Mycorrhizal Genomics Initiative is supported by the French National Institute for Agricultural Research (INRA), the US Department of Energy (DOE) Joint Genome Institute (JGI; Office of Science of the US Department of Energy), the Region Lorraine Research Council and the European Commission [European Regional Development Fund (ERDF)].

Details

Language :
English
ISSN :
1664302X
Database :
OpenAIRE
Journal :
Frontiers in Microbiology (8), 2320. (2017), Frontiers in Microbiology, Frontiers in Microbiology, Frontiers Media, 2017, 8, pp.2320. ⟨10.3389/fmicb.2017.02320⟩, Frontiers in Microbiology, Vol 8 (2017)
Accession number :
edsair.doi.dedup.....3a781f2146d80abc3c45485f3719988a
Full Text :
https://doi.org/10.3389/fmicb.2017.02320⟩