2014
DOI: 10.1007/s11816-014-0331-6
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Volatile methyl jasmonate is a transmissible form of jasmonate and its biosynthesis is involved in systemic jasmonate response in wounding

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Cited by 30 publications
(24 citation statements)
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“…Figure 2 shows that methyl-jasmonate was significantly more abundant and responsive to the grapevine/phytoplasma interaction than jasmonate was. Indeed, recent evidence reinforces the idea that methyl-jasmonate, because of its volatile nature, is more effective than jasmonate, as a transmissible signal that is able to induce systemic defence responses in plants [ 36 ]. Therefore, the increased methyl-jasmonate levels detected in both D and R plants could reflect a systemic jasmonate response following grapevine/phytoplasma interaction.…”
Section: Discussionmentioning
confidence: 84%
“…Figure 2 shows that methyl-jasmonate was significantly more abundant and responsive to the grapevine/phytoplasma interaction than jasmonate was. Indeed, recent evidence reinforces the idea that methyl-jasmonate, because of its volatile nature, is more effective than jasmonate, as a transmissible signal that is able to induce systemic defence responses in plants [ 36 ]. Therefore, the increased methyl-jasmonate levels detected in both D and R plants could reflect a systemic jasmonate response following grapevine/phytoplasma interaction.…”
Section: Discussionmentioning
confidence: 84%
“…When “damage + MeJA” was added to our vibration treatment, the level of JA was much higher than with vibration alone, suggesting that vibrations potentiated the JA response, as previously reported for glucosinolates and anthocyanins (Appel and Cocroft, 2014). Alternatively, MeJA may have been converted back to JA to interact with other metabolic pathways involved in defense responses (Koo et al, 2013; Jang et al, 2014).…”
Section: Discussionmentioning
confidence: 99%
“…GUS staining was performed as described 57 with slight modifications. AHP6::GUS/Col-0 and AHP6::GUS/myc2-3 grown in JA-treated or -untreated conditions for 7 days were incubated in GUS staining solution with or without 1 mM ferrocyanide/ferricyanide (100 mM NaPO 4 pH 7.0, 0.5 mM 5-bromo-4-chloro-3-indolyl-glucuronide, and 0.2% Triton X-100) at 37 °C for 3 or 8 h. The samples were then washed with 100 mM NaPO 4 (pH 7.0) and incubated in 70% ethanol at 4 °C overnight.…”
Section: Methodsmentioning
confidence: 99%