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First published online April 7, 2006; 10.1104/pp.106.078717

Plant Physiology 141:436-445 (2006)
© 2006 American Society of Plant Biologists

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Right arrow Reactive Oxygen Species

Transcriptomic Footprints Disclose Specificity of Reactive Oxygen Species Signaling in Arabidopsis1,[W]

Ilya Gadjev2, Sandy Vanderauwera2, Tsanko S. Gechev, Christophe Laloi, Ivan N. Minkov, Vladimir Shulaev, Klaus Apel, Dirk Inzé, Ron Mittler and Frank Van Breusegem*

Department of Plant Systems Biology, Flanders Interuniversity Institute for Biotechnology, Ghent University, B–9052 Gent, Belgium (I.G., S.V., D.I., F.V.B.); Department of Plant Physiology and Plant Molecular Biology, University of Plovdiv, Plovdiv 4000, Bulgaria (I.G., T.S.G., I.N.M.); Department Molecular Biology of Plants, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, NL–9751 NN Haren, The Netherlands (T.S.G.); Institute of Plant Sciences, Plant Genetics, Swiss Federal Institute of Technology, CH–8092 Zurich, Switzerland (C.L., K.A.); Department of Biochemistry, University of Nevada, Reno, Nevada 89557 (R.M.); and Virginia Bioinformatics Institute, Blacksburg, Virginia 24061 (V.S.)

Reactive oxygen species (ROS) are key players in the regulation of plant development, stress responses, and programmed cell death. Previous studies indicated that depending on the type of ROS (hydrogen peroxide, superoxide, or singlet oxygen) or its subcellular production site (plastidic, cytosolic, peroxisomal, or apoplastic), a different physiological, biochemical, and molecular response is provoked. We used transcriptome data generated from ROS-related microarray experiments to assess the specificity of ROS-driven transcript expression. Data sets obtained by exogenous application of oxidative stress-causing agents (methyl viologen, Alternaria alternata toxin, 3-aminotriazole, and ozone) and from a mutant (fluorescent) and transgenic plants, in which the activity of an individual antioxidant enzyme was perturbed (catalase, cytosolic ascorbate peroxidase, and copper/zinc superoxide dismutase), were compared. In total, the abundance of nearly 26,000 transcripts of Arabidopsis (Arabidopsis thaliana) was monitored in response to different ROS. Overall, 8,056, 5,312, and 3,925 transcripts showed at least a 3-, 4-, or 5-fold change in expression, respectively. In addition to marker transcripts that were specifically regulated by hydrogen peroxide, superoxide, or singlet oxygen, several transcripts were identified as general oxidative stress response markers because their steady-state levels were at least 5-fold elevated in most experiments. We also assessed the expression characteristics of all annotated transcription factors and inferred new candidate regulatory transcripts that could be responsible for orchestrating the specific transcriptomic signatures triggered by different ROS. Our analysis provides a framework that will assist future efforts to address the impact of ROS signals within environmental stress conditions and elucidate the molecular mechanisms of the oxidative stress response in plants.


1 This work was supported by the Research Fund of the Ghent University (Geconcerteerde Onderzoeksacties no. 12051403), by the Institute for the Promotion of Innovation by Science and Technology in Flanders (grant no. 040134), by the Scientific Co-operation between Eastern Europe and Switzerland program and the International Atomic Energy Agency (predoctoral fellowship to I.G.), the North Atlantic Treaty Organization (postdoctoral fellowship [RIG 981271] to T.S.G.).

2 These authors contributed equally to the paper.

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: Frank Van Breusegem (frank.vanbreusegem{at}psb.ugent.be).

[W] The online version of this article contains Web-only data.

Article, publication date, and citation information can be found at www.plantphysiol.org/cgi/doi/10.1104/pp.106.078717.

* Corresponding author; e-mail frank.vanbreusegem{at}psb.ugent.be; fax 32–9–3313809.

Received February 4, 2006; returned for revision March 28, 2006; accepted March 28, 2006.




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