Mechanisms of sDNA-induced postharvest peach resistance to Rhizopus stolonifer via PpMYC2 in the JA signaling

• sDNA acts as a DAMP that initiates PTI-related ISR defense in postharvest peach fruit. • sDNA boosts the JA master regulator PpMYC2 and activates JA-dependent defense. • PpMYC2 competes with PpNPR1, hindering the formation of the PpTGA1-PpNPR1 complex. • sDNA-inducd PpMYC2 inhibited PpTGA1-PpNPR1 module to initiate JA signaling response. Jasmonic acid acts as an essential phythormone in plant defenses against necrotrophic fungi. This study investigated the immune response induced by damage-associated molecular pattern (DAMP) molecule extracellular self-DNA (sDNA) to resistant Rhizopus stolonifer invasion in postharvest peaches through JA signaling pathway. The results confirmed that perception of sDNA inhibited R. stolonifer colonization and activated MAPK cascades. Yeast two-hybrid (Y2H) and luciferase complementation imaging (LCI) assay indicated the interaction between PpMAPK1 and PpLOX2, implying PpMAPK1 could mediate the function of PpLOX2 protein. Moreover, sDNA induced transcription of JA biosynthesis genes and JA-responsive genes, as well as the master regulator PpMYC2 in JA signaling pathway. Results of electrophoretic mobility shift assay (EMSA) indicated that PpMYC2 activated transcription of JA-responsive genes through directly bound to G-box cis -element in these genes promoter. Additionally, yeast three-hybrid (Y3H) and dual-luciferase reporter analysis (DLR) demonstrated that PpNPR1 interacted with PpMYC2 and performed as a transcriptional suppressor of PpMYC2-targeted JA-responsive genes, implying it participating in regulating antagonistic between JA- and SA-induced defense response. Finally, construction of PpROS1 overexpressor and PpROS1 cas9 mutants in peaches demonstrated that PpMYC2 functioned as a crucial regulator on sDNA-triggered resistance to necrotrophic fungi R. stolonifer via JA signaling pathway. Hence, this study elucidated the importance of JA-induced gene PpMYC2 in response to against R. stolonifer invasion in sDNA-treated postharvest peaches, thus providing insight into the regulatory function of sDNA in the JA signaling pathway.

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Publication Details

Journal
Scientia Horticulturae
Published
2026-02-01
DOI
https://doi.org/10.1016/j.scienta.2026.114690
Primary Topic
Insect-Plant Interactions and Control
Type
article
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article

Mechanisms of sDNA-induced postharvest peach resistance to Rhizopus stolonifer via PpMYC2 in the JA signaling

Kaituo Wang, Fei Xiang, Minghua Zhou, Xia Yijia et al.
Scientia Horticulturae
Insect-Plant Interactions and Control
article

Mechanisms of sDNA-induced postharvest peach resistance to Rhizopus stolonifer via PpMYC2 in the JA signaling

Kaituo Wang, Fei Xiang, Minghua Zhou, Xia Yijia, Chunhong Li, Yanyu Zou, Yonghua Zheng, Jiahao Li
article en

Abstract

• sDNA acts as a DAMP that initiates PTI-related ISR defense in postharvest peach fruit. • sDNA boosts the JA master regulator PpMYC2 and activates JA-dependent defense. • PpMYC2 competes with PpNPR1, hindering the formation of the PpTGA1-PpNPR1 complex. • sDNA-inducd PpMYC2 inhibited PpTGA1-PpNPR1 module to initiate JA signaling response. Jasmonic acid acts as an essential phythormone in plant defenses against necrotrophic fungi. This study investigated the immune response induced by damage-associated molecular pattern (DAMP) molecule extracellular self-DNA (sDNA) to resistant Rhizopus stolonifer invasion in postharvest peaches through JA signaling pathway. The results confirmed that perception of sDNA inhibited R. stolonifer colonization and activated MAPK cascades. Yeast two-hybrid (Y2H) and luciferase complementation imaging (LCI) assay indicated the interaction between PpMAPK1 and PpLOX2, implying PpMAPK1 could mediate the function of PpLOX2 protein. Moreover, sDNA induced transcription of JA biosynthesis genes and JA-responsive genes, as well as the master regulator PpMYC2 in JA signaling pathway. Results of electrophoretic mobility shift assay (EMSA) indicated that PpMYC2 activated transcription of JA-responsive genes through directly bound to G-box cis -element in these genes promoter. Additionally, yeast three-hybrid (Y3H) and dual-luciferase reporter analysis (DLR) demonstrated that PpNPR1 interacted with PpMYC2 and performed as a transcriptional suppressor of PpMYC2-targeted JA-responsive genes, implying it participating in regulating antagonistic between JA- and SA-induced defense response. Finally, construction of PpROS1 overexpressor and PpROS1 cas9 mutants in peaches demonstrated that PpMYC2 functioned as a crucial regulator on sDNA-triggered resistance to necrotrophic fungi R. stolonifer via JA signaling pathway. Hence, this study elucidated the importance of JA-induced gene PpMYC2 in response to against R. stolonifer invasion in sDNA-treated postharvest peaches, thus providing insight into the regulatory function of sDNA in the JA signaling pathway.

Scientia HorticulturaeVol. 358
Nanjing Agricultural University (CN), Chongqing Public Health Medical Center (CN), Chongqing Three Gorges University (CN)
Openalex Percentile: Top 56%
Insect-Plant Interactions and Control
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