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HvHMA2, a P(1B)-ATPase from Barley, Is Highly Conserved among Cereals and Functions in Zn and Cd Transport

Manipulation of crops to improve their nutritional value (biofortification) and optimisation of plants for removal of toxic metals from contaminated soils (phytoremediation) are major goals. Identification of membrane transporters with roles in zinc and cadmium transport would be useful for both asp...

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Autores principales: Mills, Rebecca F., Peaston, Kerry A., Runions, John, Williams, Lorraine E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3411818/
https://www.ncbi.nlm.nih.gov/pubmed/22880063
http://dx.doi.org/10.1371/journal.pone.0042640
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author Mills, Rebecca F.
Peaston, Kerry A.
Runions, John
Williams, Lorraine E.
author_facet Mills, Rebecca F.
Peaston, Kerry A.
Runions, John
Williams, Lorraine E.
author_sort Mills, Rebecca F.
collection PubMed
description Manipulation of crops to improve their nutritional value (biofortification) and optimisation of plants for removal of toxic metals from contaminated soils (phytoremediation) are major goals. Identification of membrane transporters with roles in zinc and cadmium transport would be useful for both aspects. The P(1B)-ATPases play important roles in heavy metal allocation and detoxification in Arabidopsis and it is now important to elucidate their roles in monocots. We identified nine P(1B)-ATPases in barley and this study focuses on the functional characterization of HvHMA2, providing evidence for its role in heavy metal transport. HvHMA2 was cloned using information from EST analysis and 5′ RACE. It possesses the conserved aspartate that is phosphorylated during the reaction cycle of P-type pumps and has motifs and key residues characteristic of P(1B)-ATPases, falling into the P(1B-2) subclass. Homologous sequences occur in three major sub-families of the Poaceae (Gramineae). Heterologous expression in Saccharomyces cerevisiae demonstrates that HvHMA2 functions as a Zn and Cd pump. Mutagenesis studies show that proposed cation coordination sites of the P(1B-2) pumps are crucial for the metal responses conferred by HvHMA2 in yeast. HvHMA2 expression suppresses the Zn-deficient phenotype of the Arabidopsis hma2hma4 mutant indicating that HvHMA2 functions as a Zn pump in planta and could play a role in root to shoot Zn transport. When expressed in Arabidopsis, HvHMA2 localises predominantly to the plasma membrane.
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spelling pubmed-34118182012-08-09 HvHMA2, a P(1B)-ATPase from Barley, Is Highly Conserved among Cereals and Functions in Zn and Cd Transport Mills, Rebecca F. Peaston, Kerry A. Runions, John Williams, Lorraine E. PLoS One Research Article Manipulation of crops to improve their nutritional value (biofortification) and optimisation of plants for removal of toxic metals from contaminated soils (phytoremediation) are major goals. Identification of membrane transporters with roles in zinc and cadmium transport would be useful for both aspects. The P(1B)-ATPases play important roles in heavy metal allocation and detoxification in Arabidopsis and it is now important to elucidate their roles in monocots. We identified nine P(1B)-ATPases in barley and this study focuses on the functional characterization of HvHMA2, providing evidence for its role in heavy metal transport. HvHMA2 was cloned using information from EST analysis and 5′ RACE. It possesses the conserved aspartate that is phosphorylated during the reaction cycle of P-type pumps and has motifs and key residues characteristic of P(1B)-ATPases, falling into the P(1B-2) subclass. Homologous sequences occur in three major sub-families of the Poaceae (Gramineae). Heterologous expression in Saccharomyces cerevisiae demonstrates that HvHMA2 functions as a Zn and Cd pump. Mutagenesis studies show that proposed cation coordination sites of the P(1B-2) pumps are crucial for the metal responses conferred by HvHMA2 in yeast. HvHMA2 expression suppresses the Zn-deficient phenotype of the Arabidopsis hma2hma4 mutant indicating that HvHMA2 functions as a Zn pump in planta and could play a role in root to shoot Zn transport. When expressed in Arabidopsis, HvHMA2 localises predominantly to the plasma membrane. Public Library of Science 2012-08-03 /pmc/articles/PMC3411818/ /pubmed/22880063 http://dx.doi.org/10.1371/journal.pone.0042640 Text en © 2012 Mills 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
Mills, Rebecca F.
Peaston, Kerry A.
Runions, John
Williams, Lorraine E.
HvHMA2, a P(1B)-ATPase from Barley, Is Highly Conserved among Cereals and Functions in Zn and Cd Transport
title HvHMA2, a P(1B)-ATPase from Barley, Is Highly Conserved among Cereals and Functions in Zn and Cd Transport
title_full HvHMA2, a P(1B)-ATPase from Barley, Is Highly Conserved among Cereals and Functions in Zn and Cd Transport
title_fullStr HvHMA2, a P(1B)-ATPase from Barley, Is Highly Conserved among Cereals and Functions in Zn and Cd Transport
title_full_unstemmed HvHMA2, a P(1B)-ATPase from Barley, Is Highly Conserved among Cereals and Functions in Zn and Cd Transport
title_short HvHMA2, a P(1B)-ATPase from Barley, Is Highly Conserved among Cereals and Functions in Zn and Cd Transport
title_sort hvhma2, a p(1b)-atpase from barley, is highly conserved among cereals and functions in zn and cd transport
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3411818/
https://www.ncbi.nlm.nih.gov/pubmed/22880063
http://dx.doi.org/10.1371/journal.pone.0042640
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