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First published online March 26, 2004; 10.1104/pp.103.037135

Plant Physiology 134:1672-1682 (2004)
© 2004 American Society of Plant Biologists

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ENVIRONMENTAL STRESS AND ADAPTATION

Mechanism of Gene Expression of Arabidopsis Glutathione S-Transferase, AtGST1, and AtGST11 in Response to Aluminum Stress1

Bunichi Ezaki*, Masakatsu Suzuki, Hirotoshi Motoda2, Masako Kawamura, Susumu Nakashima and Hideaki Matsumoto

Research Institute for Bioresources, Okayama University, 2–20–1, Chuou, Kurashiki, Okayama 710–0046, Japan

The gene expression of two Al-induced Arabidopsis glutathione S-transferase genes, AtGST1 and AtGST11, was analyzed to investigate the mechanism underlying the response to Al stress. An approximately 1-kb DNA fragment of the 5'-upstream region of each gene was fused to a {beta}-glucuronidase (GUS) reporter gene (pAtGST1::GUS and pAtGST11::GUS) and introduced into Arabidopsis ecotype Landsberg erecta. The constructed transgenic lines showed a time-dependent gene expression to a different degree in the root and/or leaf by Al stress. The pAtGST1::GUS gene was induced after a short Al treatment (maximum expression after a 2-h exposure), while the pAtGST11::GUS gene was induced by a longer Al treatment (approximately 8 h for maximum expression). Since the gene expression was observed in the leaf when only the root was exposed to Al stress, a signaling system between the root and shoot was suggested in Al stress. A GUS staining experiment using an adult transgenic line carrying the pAtGST11::GUS gene supported this suggestion. Furthermore, Al treatment simultaneously with various Ca depleted conditions in root region enhanced the gene expression of the pAtGST11::GUS in the shoot region. This result suggested that the degree of Al toxicity in the root reflects the gene response of pAtGST11::GUS in the shoot via the deduced signaling system. Both transgenic lines also showed an increase of GUS activity after cold stress, heat stress, metal toxicity, and oxidative damages, suggesting a common induction mechanism in response to the tested stresses including Al stress.


1 This work was supported by the Program for Promotion of Basic Research Activities for Innovative Biosciences (to H.M.), the Ministry of Education, Culture, Sports, Science and Technology [Grant-in-Aid for Scientific Research (C)(2) no. 13660066 to B.E., and Grant-in-Aid for Scientific Research (A)(2) no. 11306006 and no. 14206008 to H.M.], and two JSPS Joint Projects under the Japan-U.S. Cooperative Science program (to B.E. and to H.M.).

2 Present address: Graduate School of Medicine, Kyoto University, Konoe-cho, Yoshida, Sakyou-ku, Kyoto 606–8501, Japan.

Article, publication date, and citation information can be found at www.plantphysiol.org/cgi/doi/10.1104/pp.103.037135.

* Corresponding author; e-mail bezaki{at}rib.okayama-u.ac.jp; fax 086–434–1249.

Received December 2, 2003; returned for revision December 18, 2003; accepted December 18, 2003.




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[Abstract] [Full Text] [PDF]




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