Cargando…

Vacuolar-Iron-Transporter1-Like Proteins Mediate Iron Homeostasis in Arabidopsis

Iron deficiency is a nutritional problem in plants and reduces crop productivity, quality and yield. With the goal of improving the iron (Fe) storage properties of plants, we have investigated the function of three Arabidopsis proteins with homology to Vacuolar Iron Transporter1 (AtVIT1). Heterologo...

Descripción completa

Detalles Bibliográficos
Autores principales: Gollhofer, Julia, Timofeev, Roman, Lan, Ping, Schmidt, Wolfgang, Buckhout, Thomas J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215979/
https://www.ncbi.nlm.nih.gov/pubmed/25360591
http://dx.doi.org/10.1371/journal.pone.0110468
_version_ 1782342185130131456
author Gollhofer, Julia
Timofeev, Roman
Lan, Ping
Schmidt, Wolfgang
Buckhout, Thomas J.
author_facet Gollhofer, Julia
Timofeev, Roman
Lan, Ping
Schmidt, Wolfgang
Buckhout, Thomas J.
author_sort Gollhofer, Julia
collection PubMed
description Iron deficiency is a nutritional problem in plants and reduces crop productivity, quality and yield. With the goal of improving the iron (Fe) storage properties of plants, we have investigated the function of three Arabidopsis proteins with homology to Vacuolar Iron Transporter1 (AtVIT1). Heterologous expression of Vacuolar Iron Transporter-Like1 (AtVTL1; At1g21140), AtVTL2 (At1g76800) or AtVTL5 (At3g25190) in the yeast vacuolar Fe transport mutant, Δccc1, restored growth in the presence of 4 mM Fe. Isolated vacuoles from yeast expressing either of the VTL genes in the Δccc1 background had a three- to four-fold increase in Fe concentration compared to vacuoles isolated from the untransformed mutant. Transiently expressed GFP-tagged AtVTL1 was localized exclusively and AtVTL2 was localized primarily to the vacuolar membrane of onion epidermis cells. Seedling root growth of the Arabidopsis nramp3/nramp4 and vit1-1 mutants was decreased compared to the wild type when seedlings were grown under Fe deficiency. When expressed under the 35S promoter in the nramp3/nramp4 or vit1-1 backgrounds, AtVTL1, AtVTL2 or AtVTL5 restored root growth in both mutants. The seed Fe concentration in the nramp3/nramp4 mutant overexpressing AtVTL1, AtVTL2 or AtVTL5 was between 50 and 60% higher than in non-transformed double mutants or wild-type plants. We conclude that the VTL proteins catalyze Fe transport into vacuoles and thus contribute to the regulation of Fe homeostasis in planta.
format Online
Article
Text
id pubmed-4215979
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-42159792014-11-05 Vacuolar-Iron-Transporter1-Like Proteins Mediate Iron Homeostasis in Arabidopsis Gollhofer, Julia Timofeev, Roman Lan, Ping Schmidt, Wolfgang Buckhout, Thomas J. PLoS One Research Article Iron deficiency is a nutritional problem in plants and reduces crop productivity, quality and yield. With the goal of improving the iron (Fe) storage properties of plants, we have investigated the function of three Arabidopsis proteins with homology to Vacuolar Iron Transporter1 (AtVIT1). Heterologous expression of Vacuolar Iron Transporter-Like1 (AtVTL1; At1g21140), AtVTL2 (At1g76800) or AtVTL5 (At3g25190) in the yeast vacuolar Fe transport mutant, Δccc1, restored growth in the presence of 4 mM Fe. Isolated vacuoles from yeast expressing either of the VTL genes in the Δccc1 background had a three- to four-fold increase in Fe concentration compared to vacuoles isolated from the untransformed mutant. Transiently expressed GFP-tagged AtVTL1 was localized exclusively and AtVTL2 was localized primarily to the vacuolar membrane of onion epidermis cells. Seedling root growth of the Arabidopsis nramp3/nramp4 and vit1-1 mutants was decreased compared to the wild type when seedlings were grown under Fe deficiency. When expressed under the 35S promoter in the nramp3/nramp4 or vit1-1 backgrounds, AtVTL1, AtVTL2 or AtVTL5 restored root growth in both mutants. The seed Fe concentration in the nramp3/nramp4 mutant overexpressing AtVTL1, AtVTL2 or AtVTL5 was between 50 and 60% higher than in non-transformed double mutants or wild-type plants. We conclude that the VTL proteins catalyze Fe transport into vacuoles and thus contribute to the regulation of Fe homeostasis in planta. Public Library of Science 2014-10-31 /pmc/articles/PMC4215979/ /pubmed/25360591 http://dx.doi.org/10.1371/journal.pone.0110468 Text en © 2014 Gollhofer et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Gollhofer, Julia
Timofeev, Roman
Lan, Ping
Schmidt, Wolfgang
Buckhout, Thomas J.
Vacuolar-Iron-Transporter1-Like Proteins Mediate Iron Homeostasis in Arabidopsis
title Vacuolar-Iron-Transporter1-Like Proteins Mediate Iron Homeostasis in Arabidopsis
title_full Vacuolar-Iron-Transporter1-Like Proteins Mediate Iron Homeostasis in Arabidopsis
title_fullStr Vacuolar-Iron-Transporter1-Like Proteins Mediate Iron Homeostasis in Arabidopsis
title_full_unstemmed Vacuolar-Iron-Transporter1-Like Proteins Mediate Iron Homeostasis in Arabidopsis
title_short Vacuolar-Iron-Transporter1-Like Proteins Mediate Iron Homeostasis in Arabidopsis
title_sort vacuolar-iron-transporter1-like proteins mediate iron homeostasis in arabidopsis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215979/
https://www.ncbi.nlm.nih.gov/pubmed/25360591
http://dx.doi.org/10.1371/journal.pone.0110468
work_keys_str_mv AT gollhoferjulia vacuolarirontransporter1likeproteinsmediateironhomeostasisinarabidopsis
AT timofeevroman vacuolarirontransporter1likeproteinsmediateironhomeostasisinarabidopsis
AT lanping vacuolarirontransporter1likeproteinsmediateironhomeostasisinarabidopsis
AT schmidtwolfgang vacuolarirontransporter1likeproteinsmediateironhomeostasisinarabidopsis
AT buckhoutthomasj vacuolarirontransporter1likeproteinsmediateironhomeostasisinarabidopsis