Skip Navigation

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (4)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Hirayama, T.
Right arrow Articles by Shinozaki, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hirayama, T.
Right arrow Articles by Shinozaki, K.
Agricola
Right arrow Articles by Hirayama, T.
Right arrow Articles by Shinozaki, K.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Plant and Cell Physiology, 2004, Vol. 45, No. 6 703-711
© 2004 Oxford University Press

A Novel Ethanol-Hypersensitive Mutant of Arabidopsis

Takashi Hirayama1,2,3, Naoko Fujishige1, Takanori Kunii1, Noriyuki Nishimura1, Satoshi Iuchi2 and Kazuo Shinozaki2

1 Graduate School of Integrated Science, Yokohama City University, Yokohama, Kanagawa, 230-0045 Japan
2 RIKEN Tsukuba Institute, Tsukuba, Ibaraki, 305-0074 Japan

A novel ethanol-hypersensitive mutant, geko1 (gek1), was isolated from Arabidopsis thaliana. The gek1 mutant displays an enhanced sensitivity (10–100 times greater than the wild type) to ethanol in growth medium, while it grows normally in the absence of ethanol, and responds normally to other alcohols and to environmental stresses such as heat shock and high salinity. The ethanol-hypersensitive phenotype of gek1 requires alcohol dehydrogenase activity, indicating that gek1 is sensitive not to ethanol itself but to the metabolites of ethanol. Consistent with this, gek1 shows enhanced sensitivity to acetaldehyde in the medium. The endogenous acetaldehyde levels were not different between gek1-2 and wild-type seedlings treated with ethanol. These results indicate that the ethanol hypersensitivity of gek1 is due to an enhanced sensitivity to acetaldehyde toxicity, instead of abnormally elevated accumulation of toxic acetaldehyde, which has been thought to be the major cause of ethanol toxicity in mammal cells.

3 Corresponding author: E-mail, hirayama{at}gsc.riken.jp; Fax, +81-45-508-7363.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Nucleic Acids ResHome page
S. Wydau, M.-L. Ferri-Fioni, S. Blanquet, and P. Plateau
GEK1, a gene product of Arabidopsis thaliana involved in ethanol tolerance, is a D-aminoacyl-tRNA deacylase
Nucleic Acids Res., February 16, 2007; 35(3): 930 - 938.
[Abstract] [Full Text] [PDF]


Home page
Plant CellHome page
V. Joshi, K. M. Laubengayer, N. Schauer, A. R. Fernie, and G. Jander
Two Arabidopsis Threonine Aldolases Are Nonredundant and Compete with Threonine Deaminase for a Common Substrate Pool
PLANT CELL, December 1, 2006; 18(12): 3564 - 3575.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
M.-L. Ferri-Fioni, M. Fromant, A.-P. Bouin, C. Aubard, C. Lazennec, P. Plateau, and S. Blanquet
Identification in Archaea of a Novel D-Tyr-tRNATyr Deacylase
J. Biol. Chem., September 15, 2006; 281(37): 27575 - 27585.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
J. Kikuchi, K. Shinozaki, and T. Hirayama
Stable Isotope Labeling of Arabidopsis thaliana for an NMR-Based Metabolomics Approach
Plant Cell Physiol., August 15, 2004; 45(8): 1099 - 1104.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.