2008
DOI: 10.1104/pp.107.112029
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Cross Talk in Defense Signaling

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Cited by 895 publications
(721 citation statements)
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References 63 publications
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“…Certain volatiles even might be involved in the resistance of plants to abiotic stress (Behnke et al, 2007), and BTH treatment has been reported to enhance the attractiveness of herbivore-damaged corn seedlings to parasitic wasps (Rostás and Turlings, 2008). The more common pattern, however, appears to be that JA-and SAmediated signaling elicit very different defensive plant responses and that SA signaling suppresses JAmediated defenses (Maleck et al, 2000;Pieterse and Dicke, 2007;Korneef and Pieterse, 2008). The high specificity of the response observed here thus made A, RT-PCR shows an induction of PR-2 by direct BTH treatment (0 h) and a priming effect on this gene, which was strongly expressed 6 and 12 h after P. syringae inoculation (hpi) when plants had already been treated with 0.5 mM BTH.…”
Section: Discussionmentioning
confidence: 97%
See 1 more Smart Citation
“…Certain volatiles even might be involved in the resistance of plants to abiotic stress (Behnke et al, 2007), and BTH treatment has been reported to enhance the attractiveness of herbivore-damaged corn seedlings to parasitic wasps (Rostás and Turlings, 2008). The more common pattern, however, appears to be that JA-and SAmediated signaling elicit very different defensive plant responses and that SA signaling suppresses JAmediated defenses (Maleck et al, 2000;Pieterse and Dicke, 2007;Korneef and Pieterse, 2008). The high specificity of the response observed here thus made A, RT-PCR shows an induction of PR-2 by direct BTH treatment (0 h) and a priming effect on this gene, which was strongly expressed 6 and 12 h after P. syringae inoculation (hpi) when plants had already been treated with 0.5 mM BTH.…”
Section: Discussionmentioning
confidence: 97%
“…However, the wound response, the induction of VOCs, the effects of plant growth-promoting rhizobacteria, and even the resistance to necrotrophic pathogens such as B. cinerea and Alternaria brassiccicola are mediated via JA signaling (Wasternack and Parthier, 1997;Pieterse et al, 1998;Schilmiller and Howe, 2005;Francia et al, 2007;Heil, 2008;Heil and Ton, 2008). In contrast, systemic acquired resistance (SAR) to biotrophic pathogens in many plant species is mediated by SA signaling, which increases the expression of phytoalexins and of several PATHOGENESIS-RELATED (PR) proteins (van Loon, 1997;Hammerschmidt and SmithBecker, 1999;Durrant and Dong, 2004) and which usually is thought to act as an antagonist to JA signaling (Maleck et al, 2000;Pieterse and Dicke, 2007;Korneef and Pieterse, 2008). The volatile derivative of SA, methyl salicylate (MeSA), has been proposed as the most likely systemic signal (Park et al, 2007).…”
mentioning
confidence: 99%
“…6C), one possible explanation to this result is that other ET-responsive genes might participate, but were not included in the analysis. Cross-talk between defensesignaling pathways has been well documented [43,44] and is likely to contribute to optimize the defenses depending on the type of challenge. A crosstalk might possibly occur in AsES-induced defenses between SA-and JA-induced genes.…”
Section: Ases Induces Plant Defenses Against B Cinerea Via Sa- Jaanmentioning
confidence: 99%
“…The phytohormones SA, jasmonic acid (JA), and ethylene (ET) activate herbivore induced signals via independent, antagonistic, and synergistic pathways and interface with other hormones auxin, abscisic acid (ABA), brassinosteroid (BR), gibberellins (GA), and cytokinin (CK) [25][26][27][28]. Additionally, as part of the defense mechanisms against phloem-feeding insects and other herbivores, plants are known to alter secondary metabolites, glutathione S-transferases (GSTs), peroxidases, and redox homeostasis [19,[29][30][31].…”
Section: Introductionmentioning
confidence: 99%