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Wiley InterScience

The Plant Journal

The Plant Journal

Volume 49 Issue 1, Pages 159 - 172

Published Online: 27 Nov 2006

Journal compilation © 2010 Blackwell Publishing Ltd and the Society for Experimental Biology



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Identification of PAD2 as a γ-glutamylcysteine synthetase highlights the importance of glutathione in disease resistance of Arabidopsis
Vincent Parisy 1,† , Benoit Poinssot 1,†,‡ , Lucas Owsianowski 1 , Antony Buchala 1 , Jane Glazebrook 2 and Felix Mauch 1,*
  1 Department of Biology, University of Fribourg, Fribourg, Switzerland, and
  2 Department of Plant Biology, University of Minnesota, St Paul, MN 55109, USA
Correspondence to   * (fax +41 26 300 9740; e-mail felix.mauch@unifr.ch).
Correspondence to   The first two authors contributed equally to this paper.
Correspondence to   Present address: UMR Plante Microbe Environnement, INRA 1088, CNRS 5184, Université de Bourgogne, Dijon, France.
Copyright 2007 The Authors Journal compilation 2007 Blackwell Publishing Ltd
KEYWORDS
camalexin • Phytophthora brassicaePseudomonas syringae

ABSTRACT

The Arabidopsis pad2-1 mutant belongs to a series of non-allelic camalexin-deficient mutants. It was originally described as showing enhanced susceptibility to virulent strains of Pseudomonas syringae and was later shown to be hyper-susceptible to the oomycete pathogen Phytophthora brassicae (formerly P. porri). Surprisingly, in both pathosystems, the disease susceptibility of pad2-1 was not caused by the camalexin deficiency, suggesting additional roles of PAD2 in disease resistance. The susceptibility of pad2-1 to P. brassicae was used to map the mutation to the gene At4g23100, which encodes γ-glutamylcysteine synthetase (γ-ECS, GSH1). GSH1 catalyzes the first committed step of glutathione (GSH) biosynthesis. The pad2-1 mutation caused an S to N transition at amino acid position 298 close to the active center. The conclusion that PAD2 encodes GSH1 is supported by several lines of evidence: (i) pad2-1 mutants contained only about 22% of wild-type amounts of GSH, (ii) genetic complementation of pad2-1 with wild-type GSH1 cDNA restored GSH production, accumulation of camalexin in response to P. syringae and resistance to P. brassicae and P. syringae, (iii) another GSH1 mutant, cad2-1, showed pad2-like phenotypes, and (iv) feeding of GSH to excised leaves of pad2-1 restored camalexin production and resistance to P. brassicae. Inoculation of Col-0 with P. brassicae caused a coordinated increase in the transcript abundance of GSH1 and GSH2, the gene encoding the second enzyme in GSH biosynthesis, and resulted in enhanced foliar GSH accumulation. The pad2-1 mutant showed enhanced susceptibility to additional pathogens, suggesting an important general role of GSH in disease resistance of Arabidopsis.


Received 7 July 2006; revised 24 August 2006; accepted 20 September 2006.

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1365-313X.2006.02938.x About DOI

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