Skip Navigation

Plant and Cell Physiology 2004 45(9):1306-1312; doi:10.1093/pcp/pch135
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 (16)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Yeh, C.-M.
Right arrow Articles by Huang, H.-J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Yeh, C.-M.
Right arrow Articles by Huang, H.-J.
Agricola
Right arrow Articles by Yeh, C.-M.
Right arrow Articles by Huang, H.-J.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 2004 Oxford University Press

Short Communication

Cadmium Activates a Mitogen-Activated Protein Kinase Gene and MBP Kinases in Rice

Chuan-Ming Yeh, Lin-June Hsiao and Hao-Jen Huang1

Department of Life Sciences, Center for Biosciences and Biotechology, National Cheng Kung University, No. 1 University Road 701, Tainan, Taiwan

Abstract

Mitogen-activated protein kinase (MAPK) pathways are modules involved in the transduction of extracellular signals to intracellular targets in all eukaryotes. In plants, it has been evidenced that MAPKs play a role in the signaling of biotic and abiotic stresses, plant hormones, and cell cycle cues. However, the effect of heavy metals on plant MAPKs has not been well examined. The Northern blot analysis of OsMAPK mRNA levels has shown that only OsMAPK2, but not OsMAPK3 and OsMAPK4, expressed in suspension-cultured cells in response to 100–400 µM Cd treatments. The OsMAPK2 transcripts increased within 12 h upon 400 µM Cd treatment. In addition, we found that 42- and 50-kDa MBP kinases were significantly activated by Cd treatment in rice suspension-cultured cells. And 40-, 42-, 50- and 64-kDa MBP kinases were activated in rice roots. Furthermore, GSH inhibits Cd-induced 40-kDa MBP kinase activation. By immunoblot analysis and immunoprecipitation followed by in-gel kinase assay, we confirmed that Cd-activated 42-kDa MBP kinase is a MAP kinase. Our results suggest that a MAP kinase cascade may function in the Cd-signalling pathway in rice.

Footnotes

1 Corresponding author: E-mail, haojen{at}mail.ncku.edu.tw; Fax, +886-6-2742583.


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
J Exp BotHome page
C.-M. Yeh, P.-S. Chien, and H.-J. Huang
Distinct signalling pathways for induction of MAP kinase activities by cadmium and copper in rice roots
J. Exp. Bot., February 1, 2007; 58(3): 659 - 671.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
X. Qi, Y. Zhang, and T. Chai
Characterization of a Novel Plant Promoter Specifically Induced by Heavy Metal and Identification of the Promoter Regions Conferring Heavy Metal Responsiveness
Plant Physiology, January 1, 2007; 143(1): 50 - 59.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
A. Pitzschke and H. Hirt
Mitogen-Activated Protein Kinases and Reactive Oxygen Species Signaling in Plants
Plant Physiology, June 1, 2006; 141(2): 351 - 356.
[Full Text] [PDF]


Home page
J Exp BotHome page
M. Baier and K.-J. Dietz
Chloroplasts as source and target of cellular redox regulation: a discussion on chloroplast redox signals in the context of plant physiology
J. Exp. Bot., June 1, 2005; 56(416): 1449 - 1462.
[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.