Plant Physiol. Illumina, Inc.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


First published online October 7, 2009; 10.1104/pp.109.143735

Plant Physiology 151:1902-1917 (2009)
© 2009 American Society of Plant Biologists

OPEN ACCESS ARTICLE
This Article
Free via Open Access: OA
Right arrow OA Full Text
Right arrow Full Text (PDF)
Right arrow PPT slides of all figures
Right arrow Supplemental Data
Right arrowOA All Versions of this Article:
151/4/1902    most recent
pp.109.143735v1
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 PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Web of Science (3)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Luo, Z.-B.
Right arrow Articles by Polle, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Luo, Z.-B.
Right arrow Articles by Polle, A.
Agricola
Right arrow Articles by Luo, Z.-B.
Right arrow Articles by Polle, A.
ENVIRONMENTAL STRESS AND ADAPTATION TO STRESS

Upgrading Root Physiology for Stress Tolerance by Ectomycorrhizas: Insights from Metabolite and Transcriptional Profiling into Reprogramming for Stress Anticipation1,[C],[W],[OA]

Zhi-Bin Luo, Dennis Janz, Xiangning Jiang, Cornelia Göbel, Henning Wildhagen, Yupeng Tan, Heinz Rennenberg, Ivo Feussner and Andrea Polle*

College of Life Sciences, Northwest Agriculture & Forestry University, Yangling, Shaanxi 712100, People's Republic of China (Z.-B.L.); Büsgen Institute, Department for Forest Botany and Tree Physiology (Z.-B.L., D.J., A.P.), and Albrecht-von-Haller Institute for Plant Sciences, Department for Plant Biochemistry (C.G., I.F.), Georg-August University, 37077 Goettingen, Germany; College of Life Sciences and Biotechnology, Beijing Forestry University, Beijing 100083, People's Republic of China (X.J., Y.T.); and Institute of Forest Botany and Tree Physiology, Chair of Tree Physiology, Albert-Ludwigs University, 79110 Freiburg, Germany (H.W., H.R.)

Ectomycorrhizas (EMs) alleviate stress tolerance of host plants, but the underlying molecular mechanisms are unknown. To elucidate the basis of EM-induced physiological changes and their involvement in stress adaptation, we investigated metabolic and transcriptional profiles in EM and non-EM roots of gray poplar (Populus x canescens) in the presence and absence of osmotic stress imposed by excess salinity. Colonization with the ectomycorrhizal fungus Paxillus involutus increased root cell volumes, a response associated with carbohydrate accumulation. The stress-related hormones abscisic acid and salicylic acid were increased, whereas jasmonic acid and auxin were decreased in EM compared with non-EM roots. Auxin-responsive reporter plants showed that auxin decreased in the vascular system. The phytohormone changes in EMs are in contrast to those in arbuscular mycorrhizas, suggesting that EMs and arbuscular mycorrhizas recruit different signaling pathways to influence plant stress responses. Transcriptome analyses on a whole genome poplar microarray revealed activation of genes related to abiotic and biotic stress responses as well as of genes involved in vesicle trafficking and suppression of auxin-related pathways. Comparative transcriptome analysis indicated EM-related genes whose transcript abundances were independent of salt stress and a set of salt stress-related genes that were common to EM non-salt-stressed and non-EM salt-stressed plants. Salt-exposed EM roots showed stronger accumulation of myoinositol, abscisic acid, and salicylic acid and higher K+-to-Na+ ratio than stressed non-EM roots. In conclusion, EMs activated stress-related genes and signaling pathways, apparently leading to priming of pathways conferring abiotic stress tolerance.


1 This work was supported by the Deutsche Forschungsgemeinschaft (grants to A.P. and H.R. via FOR496 [Poplar Research Group, Germany]), by the Deutscher Akademischer Austauschdienst (postdoctoral scholarship to Z.-B.L. in the program Modern Application of Biotechnology), and by the Program for New Century Excellent Talents in Universities from the Ministry of Education of China (grant no. NCET–08–0468 to Z.-B.L.).

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: Andrea Polle (apolle{at}gwdg.de).

[C] Some figures in this article are displayed in color online but in black and white in the print edition.

[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.109.143735

* Corresponding author; e-mail apolle{at}gwdg.de.

Received June 27, 2009; accepted October 4, 2009; published October 7, 2009.




This article has been cited by other articles:


Home page
Tree PhysiolHome page
H. Wildhagen, J. Durr, B. Ehlting, and H. Rennenberg
Seasonal nitrogen cycling in the bark of field-grown Grey poplar is correlated with meteorological factors and gene expression of bark storage proteins
Tree Physiol, September 1, 2010; 30(9): 1096 - 1110.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY® THE PLANT CELL
Copyright © 2009 by the American Society of Plant Biologists