2022
DOI: 10.1111/tpj.16067
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Jasmonic acid enhances osmotic stress responses by MYC2‐mediated inhibition of protein phosphatase 2C1 and response regulators 26 transcription factor in tomato

Abstract: SUMMARY The jasmonic acid (JA) signaling pathway is involved in the plant response to drought stress. JA and other hormones synergistically regulate the drought response in plants. However, the molecular mechanism underlying this synergism remains poorly defined. In the present study, transcriptome analyses of guard cells and quantitative PCR experiments revealed that MYC2 negatively regulated the negative regulator of ABA signaling, SlPP2C1, and the type‐B response regulator in the cytokinin pathway, SlRR26, … Show more

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Cited by 20 publications
(8 citation statements)
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“…JA signaling also plays important roles to regulate drought response independently or through cooperating with ABA [52][53][54]. Drought treatment induced JA and ABA accumulation in maize with earlier induction for JA production [55].…”
Section: Discussionmentioning
confidence: 99%
“…JA signaling also plays important roles to regulate drought response independently or through cooperating with ABA [52][53][54]. Drought treatment induced JA and ABA accumulation in maize with earlier induction for JA production [55].…”
Section: Discussionmentioning
confidence: 99%
“…The crosstalk between JA and ABA has been extensively implicated. AtMYC2 acts as a transcriptional activator in abscisic acid signaling (Abe et al ., 2003), and it negatively regulates the ABA signaling negative regulator, SlPP2C1, in tomato (W. C. Zhao et al ., 2023). ABA inducibility of both ANAC019 and ANAC055 is diminished in the myc2 mutant (Jiang et al ., 2009), indicating that MYC2 serves as a central connection between JA and ABA signaling.…”
Section: Discussionmentioning
confidence: 99%
“…POD, SOD, MDA, PRO, and H 2 O 2 activities were determined using corresponding assay kits (Keming Bioengineering Institute). The H 2 O 2 production in guard cells was analyzed by using 50 μM H 2 DCFDA (Coolaber) as described previously [ 67 , 68 ]. Leaves were incubated (20 min in darkness) in a staining buffer (loading buffer containing 50 μM H 2 DCFDA and 10 mM MES–Tris, pH 6.15), and washed five times in phosphate-buffered saline to remove excess H 2 DCFDA.…”
Section: Methodsmentioning
confidence: 99%