Functional expression of AtHMA4, a P-1B-type ATPase of the Zn/Co/Cd/Pb subclass
Functional expression of AtHMA4, a P-1B-type ATPase of the Zn/Co/Cd/Pb subclass
Mechanisms are required by all organisms to maintain the concentration of essential heavy metals (e.g. Zn and Cu) within physiological limits and to minimise the detrimental effects of non-essential heavy metals (e.g. Cd). Heavy-metal P-type ATPases (HMAs) are a subgroup of the P-type ATPase superfamily that may contribute to metal homeostasis in plants. We cloned and characterised a member of this family, AtHMA4, from Arabidopsis thaliana that clusters with the Zn/Co/Cd/Pb subclass of HMAs on phylogenetic analysis. Sequencing of the AtHMA4 cDNA showed that it contained the conserved motifs found in all P-type ATPases and also motifs that are characteristic of heavy-metal ATPases. Escherichia coli mutants defective in the HMAs, CopA and ZntA , were used in functional complementation studies. AtHMA4 was able to restore growth at high [Zn] in the zntA mutant but not at high [Cu] in the copA mutant, suggesting a role in zinc transport. Heterologous expression of AtHMA4 in Saccharomyces cerevisiae made the yeast more resistant to Cd but did not affect sensitivity to other metals compared with vector-transformed controls. The organ specificity of AtHMA4 was analysed in Arabidopsis and showed that AtHMA4 was expressed in a range of tissues with highest expression in roots. AtHMA4 was upregulated in roots exposed to elevated levels of Zn and Mn but downregulated by Cd. Possible physiological roles of this transporter in Arabidopsis are discussed.
Arabidopsis thaliana, heavy metal transport, heterologous expression, metal pump, transporter
164-176
Mills, R.F.
12f9aa5c-c263-4ca8-87de-abb1b5d8a76c
Krijger, G.C.
1a05c7af-56f6-466d-aba5-0db5aa327b71
Baccarini, P.J.
9a8cdddb-7242-43a3-9612-b97cd4a5db39
Hall, J.L.
24cd62e9-4050-4514-9446-5a03949007f4
Williams, L.E.
79ee1856-3732-492b-8ac5-239749c85d9e
2003
Mills, R.F.
12f9aa5c-c263-4ca8-87de-abb1b5d8a76c
Krijger, G.C.
1a05c7af-56f6-466d-aba5-0db5aa327b71
Baccarini, P.J.
9a8cdddb-7242-43a3-9612-b97cd4a5db39
Hall, J.L.
24cd62e9-4050-4514-9446-5a03949007f4
Williams, L.E.
79ee1856-3732-492b-8ac5-239749c85d9e
Mills, R.F., Krijger, G.C., Baccarini, P.J., Hall, J.L. and Williams, L.E.
(2003)
Functional expression of AtHMA4, a P-1B-type ATPase of the Zn/Co/Cd/Pb subclass.
The Plant Journal, 35 (2), .
(doi:10.1046/j.1365-313X.2003.01790.x).
Abstract
Mechanisms are required by all organisms to maintain the concentration of essential heavy metals (e.g. Zn and Cu) within physiological limits and to minimise the detrimental effects of non-essential heavy metals (e.g. Cd). Heavy-metal P-type ATPases (HMAs) are a subgroup of the P-type ATPase superfamily that may contribute to metal homeostasis in plants. We cloned and characterised a member of this family, AtHMA4, from Arabidopsis thaliana that clusters with the Zn/Co/Cd/Pb subclass of HMAs on phylogenetic analysis. Sequencing of the AtHMA4 cDNA showed that it contained the conserved motifs found in all P-type ATPases and also motifs that are characteristic of heavy-metal ATPases. Escherichia coli mutants defective in the HMAs, CopA and ZntA , were used in functional complementation studies. AtHMA4 was able to restore growth at high [Zn] in the zntA mutant but not at high [Cu] in the copA mutant, suggesting a role in zinc transport. Heterologous expression of AtHMA4 in Saccharomyces cerevisiae made the yeast more resistant to Cd but did not affect sensitivity to other metals compared with vector-transformed controls. The organ specificity of AtHMA4 was analysed in Arabidopsis and showed that AtHMA4 was expressed in a range of tissues with highest expression in roots. AtHMA4 was upregulated in roots exposed to elevated levels of Zn and Mn but downregulated by Cd. Possible physiological roles of this transporter in Arabidopsis are discussed.
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Submitted date: 13 February 2003
Published date: 2003
Keywords:
Arabidopsis thaliana, heavy metal transport, heterologous expression, metal pump, transporter
Organisations:
Biological Sciences
Identifiers
Local EPrints ID: 35530
URI: http://eprints.soton.ac.uk/id/eprint/35530
ISSN: 0960-7412
PURE UUID: aa80c6de-c6fd-44ba-801a-d7f277af95c4
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Date deposited: 18 May 2006
Last modified: 15 Mar 2024 07:52
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Contributors
Author:
R.F. Mills
Author:
G.C. Krijger
Author:
P.J. Baccarini
Author:
J.L. Hall
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