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Enhancing the aluminium tolerance of barley by expressing the citrate transporter genes SbMATE and FRD3
Malate and citrate efflux from root apices is a mechanism of Al(3+) tolerance in many plant species. Citrate efflux is facilitated by members of the MATE (multidrug and toxic compound exudation) family localized to the plasma membrane of root cells. Barley (Hordeum vulgare) is among the most Al(3+)-...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4036506/ https://www.ncbi.nlm.nih.gov/pubmed/24692647 http://dx.doi.org/10.1093/jxb/eru121 |
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author | Zhou, Gaofeng Pereira, Jorge F. Delhaize, Emmanuel Zhou, Meixue Magalhaes, Jurandir V. Ryan, Peter R. |
author_facet | Zhou, Gaofeng Pereira, Jorge F. Delhaize, Emmanuel Zhou, Meixue Magalhaes, Jurandir V. Ryan, Peter R. |
author_sort | Zhou, Gaofeng |
collection | PubMed |
description | Malate and citrate efflux from root apices is a mechanism of Al(3+) tolerance in many plant species. Citrate efflux is facilitated by members of the MATE (multidrug and toxic compound exudation) family localized to the plasma membrane of root cells. Barley (Hordeum vulgare) is among the most Al(3+)-sensitive cereal species but the small genotypic variation in tolerance that is present is correlated with citrate efflux via a MATE transporter named HvAACT1. This study used a biotechnological approach to increase the Al(3+) tolerance of barley by transforming it with two MATE genes that encode citrate transporters: SbMATE is the major Al(3+)-tolerance gene from sorghum whereas FRD3 is involved with Fe nutrition in Arabidopsis. Independent transgenic and null T3 lines were generated for both transgenes. Lines expressing SbMATE showed Al(3+)-activated citrate efflux from root apices and greater tolerance to Al(3+) toxicity than nulls in hydroponic and short-term soil trials. Transgenic lines expressing FRD3 exhibited similar phenotypes except citrate release from roots occurred constitutively. The Al(3+) tolerance of these lines was compared with previously generated transgenic barley lines overexpressing the endogenous HvAACT1 gene and the TaALMT1 gene from wheat. Barley lines expressing TaALMT1 showed significantly greater Al(3+) tolerance than all lines expressing MATE genes. This study highlights the relative efficacy of different organic anion transport proteins for increasing the Al(3+) tolerance of an important crop species. |
format | Online Article Text |
id | pubmed-4036506 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40365062014-05-28 Enhancing the aluminium tolerance of barley by expressing the citrate transporter genes SbMATE and FRD3 Zhou, Gaofeng Pereira, Jorge F. Delhaize, Emmanuel Zhou, Meixue Magalhaes, Jurandir V. Ryan, Peter R. J Exp Bot Research Paper Malate and citrate efflux from root apices is a mechanism of Al(3+) tolerance in many plant species. Citrate efflux is facilitated by members of the MATE (multidrug and toxic compound exudation) family localized to the plasma membrane of root cells. Barley (Hordeum vulgare) is among the most Al(3+)-sensitive cereal species but the small genotypic variation in tolerance that is present is correlated with citrate efflux via a MATE transporter named HvAACT1. This study used a biotechnological approach to increase the Al(3+) tolerance of barley by transforming it with two MATE genes that encode citrate transporters: SbMATE is the major Al(3+)-tolerance gene from sorghum whereas FRD3 is involved with Fe nutrition in Arabidopsis. Independent transgenic and null T3 lines were generated for both transgenes. Lines expressing SbMATE showed Al(3+)-activated citrate efflux from root apices and greater tolerance to Al(3+) toxicity than nulls in hydroponic and short-term soil trials. Transgenic lines expressing FRD3 exhibited similar phenotypes except citrate release from roots occurred constitutively. The Al(3+) tolerance of these lines was compared with previously generated transgenic barley lines overexpressing the endogenous HvAACT1 gene and the TaALMT1 gene from wheat. Barley lines expressing TaALMT1 showed significantly greater Al(3+) tolerance than all lines expressing MATE genes. This study highlights the relative efficacy of different organic anion transport proteins for increasing the Al(3+) tolerance of an important crop species. Oxford University Press 2014-06 2014-04-01 /pmc/articles/PMC4036506/ /pubmed/24692647 http://dx.doi.org/10.1093/jxb/eru121 Text en © The Author 2014. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Zhou, Gaofeng Pereira, Jorge F. Delhaize, Emmanuel Zhou, Meixue Magalhaes, Jurandir V. Ryan, Peter R. Enhancing the aluminium tolerance of barley by expressing the citrate transporter genes SbMATE and FRD3 |
title | Enhancing the aluminium tolerance of barley by expressing the citrate transporter genes SbMATE and FRD3
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title_full | Enhancing the aluminium tolerance of barley by expressing the citrate transporter genes SbMATE and FRD3
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title_fullStr | Enhancing the aluminium tolerance of barley by expressing the citrate transporter genes SbMATE and FRD3
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title_full_unstemmed | Enhancing the aluminium tolerance of barley by expressing the citrate transporter genes SbMATE and FRD3
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title_short | Enhancing the aluminium tolerance of barley by expressing the citrate transporter genes SbMATE and FRD3
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title_sort | enhancing the aluminium tolerance of barley by expressing the citrate transporter genes sbmate and frd3 |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4036506/ https://www.ncbi.nlm.nih.gov/pubmed/24692647 http://dx.doi.org/10.1093/jxb/eru121 |
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