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First published online September 20, 2007; 10.1104/pp.107.102335

Plant Physiology 145:843-852 (2007)
© 2007 American Society of Plant Biologists

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ENVIRONMENTAL STRESS AND ADAPTATION TO STRESS

Characterization of AtALMT1 Expression in Aluminum-Inducible Malate Release and Its Role for Rhizotoxic Stress Tolerance in Arabidopsis1,[W],[OA]

Yuriko Kobayashi2,3, Owen A. Hoekenga2, Hirotaka Itoh, Midori Nakashima, Shoichiro Saito, Jon E. Shaff, Lyza G. Maron, Miguel A. Piñeros, Leon V. Kochian and Hiroyuki Koyama*

Laboratory of Plant Cell Technology, Faculty of Applied Biological Sciences, Gifu University, 1-1 Yanagido Gifu 501–1193, Japan (Y.K., H.I., M.N., S.S., H.K.); and United States Plant, Soil, and Nutrition Laboratory, United States Department of Agriculture-Agricultural Research Service, Ithaca, New York 14853 (O.A.H., J.E.S., L.G.M., M.A.P., L.V.K.)

Malate transporters play a critical role in aluminum (Al) tolerance responses for some plant species, such as Arabidopsis (Arabidopsis thaliana). Here, we further characterize AtALMT1, an Arabidopsis aluminum-activated malate transporter, to clarify its specific role in malate release and Al stress responses. Malate excretion from the roots of accession Columbia was sharply induced by Al, which is concomitant with the induction of AtALMT1 gene expression. The malate release was specific for Al among rhizotoxic stressors, namely cadmium, copper, erbium, lanthanum, sodium, and low pH, which accounts for the specific sensitivity of a null mutant to Al stress. Al-specific malate excretion can be explained by a combined regulation of AtALMT1 expression and activation of AtALMT1 protein, which is specific for Al. Although low pH treatment slightly induced gene expression, other treatments did not. In addition, malate excretion in Al-activated seedlings was rapidly stopped by removing Al from the solution. Other rhizotoxic stressors were not effective in maintaining malate release. Protein kinase and phosphatase inhibitor studies indicated that reversible phosphorylation was important for the transcriptional and posttranslational regulation of AtALMT1. AtALMT1 promoter-beta-glucuronidase fusion lines revealed that AtALMT1 has restricted expression within the root, such that unnecessary carbon loss is likely minimized. Lastly, a natural nonsense mutation allele of AtALMT1 was identified from the Al-hypersensitive natural accession Warschau-1.


1 This work was supported by the Japan Society for the Promotion of Science-National Science Foundation research cooperative program and the Ministry of Economy, Trade and Industry for a joint research project between Gifu University and the Research Institute of Innovative Technology for the Earth.

2 These authors contributed equally to the article.

3 Present address: Forestry Research Institute, Oji Paper Company, 24-9 Nobono-cho Kameyama Mie 519–0212, Japan.

The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Hiroyuki Koyama (koyama{at}gifu-u.ac.jp).

[W] The online version of this article contains Web-only data.

[OA] Open Access articles can be viewed online without a subscription.

www.plantphysiol.org/cgi/doi/10.1104/pp.107.102335

* Corresponding author; e-mail koyama{at}gifu-u.ac.jp.

Received May 14, 2007; accepted September 9, 2007; published September 20, 2007.




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