Please use this identifier to cite or link to this item: http://223.31.159.10:8080/jspui/handle/123456789/1540
Full metadata record
DC FieldValueLanguage
dc.contributor.authorTiwari, Ruchi-
dc.contributor.authorGarg, Kajal-
dc.contributor.authorSenthil-Kumar, Muthappa-
dc.contributor.authorBisht, Naveen C.-
dc.date.accessioned2023-11-15T04:54:10Z-
dc.date.available2023-11-15T04:54:10Z-
dc.date.issued2024-
dc.identifier.citationPlant Journal, 117(2): 616-631en_US
dc.identifier.issn0960-7412-
dc.identifier.issn1365-313X-
dc.identifier.otherhttps://doi.org/10.1111/tpj.16518-
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1111/tpj.16518-
dc.identifier.urihttp://223.31.159.10:8080/jspui/handle/123456789/1540-
dc.descriptionAccepted date: 13 October 2023en_US
dc.description.abstractThe membrane-bound heterotrimeric G-proteins in plants play a crucial role in defending against a broad range of pathogens. This study emphasizes the significance of Extra-large Gα protein 2 (XLG2), a plant-specific G-protein, in mediating the plant response to Sclerotinia sclerotiorum, which infects over 600 plant species worldwide. Our analysis of Arabidopsis G-protein mutants showed that loss of XLG2 function increased susceptibility to S. sclerotiorum, accompanied by compromised accumulation of jasmonic acid (JA) during pathogen infection. Overexpression of the XLG2 gene in xlg2 mutant plants resulted in higher resistance and increased JA accumulation during S. sclerotiorum infection. Co-immunoprecipitation (co-IP) analysis on S. sclerotiorum infected Col-0 samples, using two different approaches, identified 201 XLG2-interacting proteins. The identified JA-biosynthetic and JA-responsive proteins had compromised transcript expression in the xlg2 mutant during pathogen infection. XLG2 was found to interact physically with a JA-responsive protein, Coronatine induced 1 (CORI3) in Co-IP, and confirmed using split firefly luciferase complementation and bimolecular fluorescent complementation assays. Additionally, genetic analysis revealed an additive effect of XLG2 and CORI3 on resistance against S. sclerotiorum, JA accumulation, and expression of the defense marker genes. Overall, our study reveals two independent pathways involving XLG2 and CORI3 in contributing resistance against S. sclerotiorum.en_US
dc.description.sponsorshipThe Plant Growth Facility, Proteomics and Mass Spectrometry Facility, Metabolome Facility (BT/INF/22/SP28268/2018), and Confocal facility at NIPGR are acknowledged. We thank Dr. Amar Pal Singh for sharing the split luciferase and BiFC vectors; Dr. Urano Daisuke and Dr. Dinesh Kumar Jaiswal for providing the Arabidopsis mutant seeds. The work was funded by the Science and Engineering Board, India (grant no. EMR/2016/006433) and a partial core grant from the NIPGR to N.C.B. R.T. was supported by a fellowship from DBT (DBT/JRF/BET-16/I/2016/AL/138).en_US
dc.language.isoen_USen_US
dc.publisherJohn Wiley & Sonsen_US
dc.subjectSclerotinia sclerotiorumen_US
dc.subjectco-immunoprecipitationen_US
dc.subjectcoronatine induced 1 (CORI3)en_US
dc.subjectextra-large Gα protein 2 (XLG2)en_US
dc.subjectjasmonic aciden_US
dc.subjectplant defenseen_US
dc.titleXLG2 and CORI3 function additively to regulate plant defense against the necrotrophic pathogen Sclerotinia sclerotiorumen_US
dc.typeArticleen_US
Appears in Collections:Institutional Publications

Files in This Item:
File Description SizeFormat 
Bisht NC_2023_4.pdf
  Restricted Access
7.94 MBAdobe PDFView/Open Request a copy


Items in IR@NIPGR are protected by copyright, with all rights reserved, unless otherwise indicated.