The WRKY70 Transcription Factor: A Node of Convergence for Jasmonate-Mediated and Salicylate-Mediated Signals in Plant Defense On-line version contains Web-only data.

By Jing Li, Günter Brader, E. Palva. The Plant Cell Online, 2004

1,171 citations recorded by the source corpus.

Subfields: Insect Science, Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/5762e04a4899928e55a6c3093c43aabe7e144d2f

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Citations in the corpus

A Genomic Approach to Identify Regulatory Nodes in the Transcriptional Network of Systemic Acquired Resistance in Plants (2006, background): “Supporting evidence came from a report where WRKY70-overexpressing plants showed constitutive resistance to two bacterial pathogens [20].”
Plant hormone-mediated regulation of stress responses (2016, background): “Although most studies prove antagonistic interaction between SA and JA, synergistic interactions have been observed at low SA-JA concentrations and by simultaneous induction of both defenses [45, 46].”
Arabidopsis WRKY33 transcription factor is required for resistance to necrotrophic fungal pathogens. (2006, background): “Our findings are similar to what was reported recently for the WRKY70 gene; basal expression levels of WRKY70 in the coi1 mutant were higher than in the wild-type plants (Li et al., 2004a; AbuQamar et al., 2006).”
Phytohormonal signaling in plant responses to aphid feeding (2011, background): “However, Li et al. (2004) reported that WRKY70 is a common component in SA and JA-mediated signal pathways and modulation of WRKY70 transcript levels by constitutive over-expression is only known to increase resistance to virulent pathogens and results in the constitutive expression of PR genes,…”
Genetic improvement of C4 grasses as cellulosic biofuel feedstocks (2009, background): “WRKY TFs have been shown to act at the junction between the jasmonic and the salicylic acid pathways, thereby modifying the crosstalk between these pathways (Li et al. 2004; Mao et al. 2007; Higashi et al. 2008) and defining the plant defense response to pathogen attack.”
Jasmonate‐regulated Arabidopsis stress signalling network (2005, background): “WRKY70 mRNA levels are enhanced in a coi1-1 background, suggesting that JA represses its expression.”
Jasmonate Biosynthesis, Perception and Function in Plant Development and Stress Responses (2013, background): “In contrast, suppression of WRKY70 leads to increased expression of JA-responsive genes and increased resistance to a pathogen sensitive to JA-dependent defenses (Li et al., 2004).”
Insights into the role of jasmonic acid-mediated defenses against necrotrophic and biotrophic fungal pathogens (2012, background): “The authors speculate that JA production may be required in some cases for the synthesis Table 1 The phenotypes of JA-related mutants when challenged with necrotrophic fungi L. esculentum (Tomato) Fusarium species jai1 Susceptible Thaler et al., 2004 L. esculentum (Tomato) B. cinerea jai1 Susceptibl”
Abiotic Stress Response in Plants - Physiological, Biochemical and Genetic Perspectives (2011, background): “In contrast, over-expression of WRKY70 results in the constitutive expression of SA-responsive PR genes and enhanced resistance to SA-sensitive pathogens but reduces resistance to JA-sensitive pathogens (Li et al., 2004).”