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Functional analysis of the rice vacuolar zinc transporter OsMTP1

Heavy metal homeostasis is maintained in plant cells by specialized transporters which compartmentalize or efflux metal ions, maintaining cytosolic concentrations within a narrow range. OsMTP1 is a member of the cation diffusion facilitator (CDF)/metal tolerance protein (MTP) family of metal cation...

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Autores principales: Menguer, Paloma K., Farthing, Emily, Peaston, Kerry A., Ricachenevsky, Felipe Klein, Fett, Janette Palma, Williams, Lorraine E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3697945/
https://www.ncbi.nlm.nih.gov/pubmed/23761487
http://dx.doi.org/10.1093/jxb/ert136
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author Menguer, Paloma K.
Farthing, Emily
Peaston, Kerry A.
Ricachenevsky, Felipe Klein
Fett, Janette Palma
Williams, Lorraine E.
author_facet Menguer, Paloma K.
Farthing, Emily
Peaston, Kerry A.
Ricachenevsky, Felipe Klein
Fett, Janette Palma
Williams, Lorraine E.
author_sort Menguer, Paloma K.
collection PubMed
description Heavy metal homeostasis is maintained in plant cells by specialized transporters which compartmentalize or efflux metal ions, maintaining cytosolic concentrations within a narrow range. OsMTP1 is a member of the cation diffusion facilitator (CDF)/metal tolerance protein (MTP) family of metal cation transporters in Oryza sativa, which is closely related to Arabidopsis thaliana MTP1. Functional complementation of the Arabidopsis T-DNA insertion mutant mtp1-1 demonstrates that OsMTP1 transports Zn in planta and localizes at the tonoplast. When heterologously expressed in the yeast mutant zrc1 cot1, OsMTP1 complemented its Zn hypersensitivity and was also localized to the vacuole. OsMTP1 alleviated, to some extent, the Co sensitivity of this mutant, rescued the Fe hypersensitivity of the ccc1 mutant at low Fe concentrations, and restored growth of the Cd-hypersensitive mutant ycf1 at low Cd concentrations. These results suggest that OsMTP1 transports Zn but also Co, Fe, and Cd, possibly with lower affinity. Site-directed mutagenesis studies revealed two substitutions in OsMTP1 that alter the transport function of this protein. OsMTP1 harbouring a substitution of Leu82 to a phenylalanine can still transport low levels of Zn, with an enhanced affinity for Fe and Co, and a gain of function for Mn. A substitution of His90 with an aspartic acid completely abolishes Zn transport but improves Fe transport in OsMTP1. These amino acid residues are important in determining substrate specificity and may be a starting point for refining transporter activity in possible biotechnological applications, such as biofortification and phytoremediation.
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spelling pubmed-36979452014-07-01 Functional analysis of the rice vacuolar zinc transporter OsMTP1 Menguer, Paloma K. Farthing, Emily Peaston, Kerry A. Ricachenevsky, Felipe Klein Fett, Janette Palma Williams, Lorraine E. J Exp Bot Research Paper Heavy metal homeostasis is maintained in plant cells by specialized transporters which compartmentalize or efflux metal ions, maintaining cytosolic concentrations within a narrow range. OsMTP1 is a member of the cation diffusion facilitator (CDF)/metal tolerance protein (MTP) family of metal cation transporters in Oryza sativa, which is closely related to Arabidopsis thaliana MTP1. Functional complementation of the Arabidopsis T-DNA insertion mutant mtp1-1 demonstrates that OsMTP1 transports Zn in planta and localizes at the tonoplast. When heterologously expressed in the yeast mutant zrc1 cot1, OsMTP1 complemented its Zn hypersensitivity and was also localized to the vacuole. OsMTP1 alleviated, to some extent, the Co sensitivity of this mutant, rescued the Fe hypersensitivity of the ccc1 mutant at low Fe concentrations, and restored growth of the Cd-hypersensitive mutant ycf1 at low Cd concentrations. These results suggest that OsMTP1 transports Zn but also Co, Fe, and Cd, possibly with lower affinity. Site-directed mutagenesis studies revealed two substitutions in OsMTP1 that alter the transport function of this protein. OsMTP1 harbouring a substitution of Leu82 to a phenylalanine can still transport low levels of Zn, with an enhanced affinity for Fe and Co, and a gain of function for Mn. A substitution of His90 with an aspartic acid completely abolishes Zn transport but improves Fe transport in OsMTP1. These amino acid residues are important in determining substrate specificity and may be a starting point for refining transporter activity in possible biotechnological applications, such as biofortification and phytoremediation. Oxford University Press 2013-07 2013-06-27 /pmc/articles/PMC3697945/ /pubmed/23761487 http://dx.doi.org/10.1093/jxb/ert136 Text en © The Author [2013]. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Menguer, Paloma K.
Farthing, Emily
Peaston, Kerry A.
Ricachenevsky, Felipe Klein
Fett, Janette Palma
Williams, Lorraine E.
Functional analysis of the rice vacuolar zinc transporter OsMTP1
title Functional analysis of the rice vacuolar zinc transporter OsMTP1
title_full Functional analysis of the rice vacuolar zinc transporter OsMTP1
title_fullStr Functional analysis of the rice vacuolar zinc transporter OsMTP1
title_full_unstemmed Functional analysis of the rice vacuolar zinc transporter OsMTP1
title_short Functional analysis of the rice vacuolar zinc transporter OsMTP1
title_sort functional analysis of the rice vacuolar zinc transporter osmtp1
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3697945/
https://www.ncbi.nlm.nih.gov/pubmed/23761487
http://dx.doi.org/10.1093/jxb/ert136
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