The Arabidopsis eATP receptor DORN1 and CNGC19 calcium channel act in tandem to regulate plant defense upon Spodoptera litura herbivory

dc.contributor.authorKundu, Pritha
dc.contributor.authorKumari, Misha
dc.contributor.authorMeena, Mukesh Kumar
dc.contributor.authorMishra, Shruti
dc.contributor.authorVadassery, Jyothilakshmi
dc.date.accessioned2025-01-27T06:41:40Z
dc.date.available2025-01-27T06:41:40Z
dc.date.issued2025
dc.descriptionAccepted date: 25 January 2025en_US
dc.description.abstractPlants deploy cellular Ca2+ elevation as a signal for environmental stress signaling. Extracellular ATP (eATP) is released into the extracellular matrix when cells are wounded. DOES NOT RESPOND TO NUCLEOTIDES 1 (DORN1), a key legume-type lectin receptor, senses and binds eATP and activates Ca2+ signaling. No evidence directly links calcium-mediated eATP signaling to resistance against insect herbivores. Here, we report upregulation of DORN1 transcripts upon wounding and Spodoptera litura feeding in Arabidopsis. Loss-of-function of DORN1 resulted in increased S. litura feeding compared to that on wildtype. Plant immunity is compromised in dorn1 mutants as they show reduced S. litura oral secretion mediated Ca2+ elevation, jasmonic acid accumulation, and expression of jasmonate responsive genes. The herbivory-induced calcium channel, CYCLIC NUCLEOTIDE GATED CHANNEL 19 (CNGC19), co-expresses with DORN1. We found that eATP-induced Ca2+ elevation requires functional CNGC19. Loss-of-function of DORN1 and CNGC19 highly increased the susceptibility to S. litura, mediated by reduced accumulation of jasmonates. We also demonstrate a plausible interaction of CNGC19 with DORN1. The data implicate the role of damage-released eATP and its receptor DORN1 in herbivory-induced defense signaling. DORN1 together with the Ca2+ channel CNGC19 generate the eATP-induced Ca2+ elevation, leading to the activation of immune signaling.en_US
dc.description.sponsorshipWe acknowledge the Department of Biotechnology (DBT), Government of India, NIPGR core grant and EMBO Global Investigator Network for funding the work. We acknowledge student funding from: DBT-BioCare for PK, UGC-NET / JRF (191620185954) for MK, UGC-NET / JRF for SM. We acknowledge NIPGR Metabolome facility (funded by DBT (BT/INF/22/SP28268/2018)) for phytohormone quantification. We also acknowledge the NIPGR central instrumentation, phytotron facility and DBT-eLibrary Consortium (DeLCON) for providing access to e-resources. This work was funded by the Department of Biotechnology (DBT), India through NIPGR core grant.en_US
dc.identifier.citationJournal of Experimental Botany, 76(8): 2264-2277en_US
dc.identifier.issn1460-2431
dc.identifier.issn0022-0957
dc.identifier.otherhttps://doi.org/10.1093/jxb/eraf025
dc.identifier.urihttps://academic.oup.com/jxb/advance-article/doi/10.1093/jxb/eraf025/7979201?login=true
dc.identifier.urihttps://ndkr-library.nipgr.ac.in/handle/123456789/1685
dc.language.isoen_USen_US
dc.publisherOxford University Pressen_US
dc.subjectAtCNGC19en_US
dc.subjectAtDORN1en_US
dc.subjectCa2+ signalingen_US
dc.subjectDAMPsen_US
dc.subjectExtracellular ATP (eATP)en_US
dc.subjectdefense phytohormonesen_US
dc.subjectinsect herbivoryen_US
dc.titleThe Arabidopsis eATP receptor DORN1 and CNGC19 calcium channel act in tandem to regulate plant defense upon Spodoptera litura herbivoryen_US
dc.typeArticleen_US

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