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 (17)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Sasaki, K.
Right arrow Articles by Ohashi, Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sasaki, K.
Right arrow Articles by Ohashi, Y.
Agricola
Right arrow Articles by Sasaki, K.
Right arrow Articles by Ohashi, Y.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Plant and Cell Physiology, 2002, Vol. 43, No. 1 108-117
© 2002 Oxford University Press

A Wound-Inducible Tobacco Peroxidase Gene Expresses Preferentially in the Vascular System

Katsutomo Sasaki1,3, Susumu Hiraga1, Hiroyuki Ito1, Shigemi Seo3, Hirokazu Matsui1 and Yuko Ohashi2,3,4

1 Department of Applied Biosciences, Graduate School of Agriculture, Hokkaido University Sapporo, 060-8589 Japan 2 Molecular Genetics Department, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki, 305-8602 Japan 3 Core Research for Evolutional Science and Technology (CREST), Ochanomizu, Chiyoda-ku, Tokyo 101-0062, Japan

A tobacco peroxidase gene tpoxN1 was reported to be expressed within 1 h after wounding in leaves [Hiraga et al. (2000a) Plant Cell Physiol. 41: 165]. We describe here further results on the wound-induced tpoxN1 expression. The quick tpoxN1 induction occurred preferentially in stems and petioles, but was negligible in leaf blades even 8 h after wounding. Induced GUS activity was also detected rapidly after wounding in the stem of transgenic tobacco plants carrying the tpoxN1 promoter::GUS fusion gene, localized mainly in the vascular systems where it was maintained this level for 14 d or more. Strong GUS activity was also found in the petiole and veinlet as well as the epidermal tissue in the stem. Treatment of known inducers for wound-responsive genes such as jasmonate, 1-aminocyclopropane-1-carboxylate, spermine, phytohormones and other stress treatments did not enhance wound-induced tpoxN1 gene expression in stems at all, but rather repressed it in some cases. Studies using metabolic inhibitors suggested that phosphorylation and dephosphorylation of proteins together with de novo protein synthesis are likely to be involved in the wound-induced tpoxN1 expression as well as some other wound-responsive genes. Thus, tpoxN1 is a unique wound-inducible and possible wound-healing gene which is rapidly expressed being maintained for a long time in veins via an unknown wound-signaling pathway(s).

4 Corresponding author: E-mail, yohashi@affrc.go.jp; Fax; +81-298-38-7469.


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
Plant Cell PhysiolHome page
K. Gomi, D. Ogawa, S. Katou, H. Kamada, N. Nakajima, H. Saji, T. Soyano, M. Sasabe, Y. Machida, I. Mitsuhara, et al.
A Mitogen-activated Protein Kinase NtMPK4 Activated by SIPKK is Required for Jasmonic Acid Signaling and Involved in Ozone Tolerance via Stomatal Movement in Tobacco
Plant Cell Physiol., December 1, 2005; 46(12): 1902 - 1914.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
K. Sasaki, T. Iwai, S. Hiraga, K. Kuroda, S. Seo, I. Mitsuhara, A. Miyasaka, M. Iwano, H. Ito, H. Matsui, et al.
Ten Rice Peroxidases Redundantly Respond to Multiple Stresses Including Infection with Rice Blast Fungus
Plant Cell Physiol., October 15, 2004; 45(10): 1442 - 1452.
[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.