The Outcomes of Concentration-Specific Interactions between Salicylate and Jasmonate Signaling Include Synergy, Antagonism, and Oxidative Stress Leading to Cell Death
By L. Mur, P. Kenton, R. Atzorn, O. Miersch, C. Wasternack. Plant Physiology, 2005
848 citations recorded by the source corpus.
Subfields: Insect Science, Plant Science
View Paper: https://www.semanticscholar.org/paper/d2162d84ea121ba14e93871f03ee34a62fa56a70
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Insect Science
- C. Pieterse
- C. Wasternack
- R. Gols
- Camille Ponzio
- D. Hodges
- Antonio León-Reyes
- I. Somssich
- Richard W. Michelmore
In Plant Science
- C. Pieterse
- M. Dicke
- C. Wasternack
- Saskia C. M. Van Wees
- Antonio León-Reyes
- Irene A. Vos
- S. V. Wees
- Shree P. Pandey
Citations in the corpus
- Jasmonate Biosynthesis, Perception and Function in Plant Development and Stress Responses (2013, background): “2 is suppressed, suggesting the interaction between these pathways may be dose dependent (Mur et al., 2006).”
- Methyl jasmonate alleviates cadmium toxicity in Solanum nigrum by regulating metal uptake and antioxidative capacity (2015, background): “A high dose of MeJA can initiate oxidative stress (Mur et al. 2006), which induces damage to the physiological barriers and results in a free flow of Cd to the tissue.”
- Networking by small-molecule hormones in plant immunity. (2009, background): “Although many reports describe an antagonistic interaction between SA- and JA-dependent signaling, synergistic interactions have been described as wel”
- Systemic acquired resistance: turning local infection into global defense. (2013, neutral): “Both synergistic and antagonistic interactions between SA and JA have been reported, suggesting that the interaction is either concentration dependent (96) or tissue specific and dynamic.”
- Ecological and phytohormonal aspects of plant volatile emission in response to single and dual infestations with herbivores and phytopathogens (2013, background): “higher concentrations or prolonged treatment duration this effect disappears, indicating that there may be threshold levels for defence trade-offs (Mur et al. 2006; Kazan & Manners 2008).”
- Quality of fresh-cut fruits and vegetables as affected by exposure to abiotic stress (2008, background): “Jasmonic acid, auxin and abscisic acid, as well as active oxygen species (AOS), have all been associated with wounding of tissues of numerous plant species (Swamy and Smith, 1999; Hodges et al., 2004; Mur et al., 2006; Takabatake et al., 2006).”
- Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, neutral): “Although there is evidence for both positive and negative relationships between these pathways (Mur et al., 2006; Truman et al., 2007), the primary mode of interaction appears to be mutual antagonism with corresponding trade-offs between resistance to”
- Jasmonates: biosynthesis, perception, signal transduction and action in plant stress response, growth and development. An update to the 2007 review in Annals of Botany. (2013, background): “…of one pathway and its antagonistic interaction with another pathway has been repeatedly demonstrated (Koornneef and Pieterse, 2008; Pieterse et al., 2012) and can be shifted from an antagonistic to synergistic interaction depending on SA and JA concentrations (Wees et al., 2000; Mur et al., 2006).”
- Plant NBS-LRR proteins: adaptable guards (2006, background): “ing pathways, involving both synergism and mutual antagonism between pathways [88-91].”
- Interplay between reactive oxygen species and hormones in the control of plant development and stress tolerance. (2015, background): “An antagonistic relationship between SA and JA signalling is observed when these hormones are present at high concentrations, and this often results in the establishment of an oxidative burst and cell death (Mur et al., 2006).”