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DC Field | Value | Language |
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dc.contributor.author | Tiwari, Ruchi | - |
dc.contributor.author | Garg, Kajal | - |
dc.contributor.author | Senthil-Kumar, Muthappa | - |
dc.contributor.author | Bisht, Naveen C. | - |
dc.date.accessioned | 2023-11-15T04:54:10Z | - |
dc.date.available | 2023-11-15T04:54:10Z | - |
dc.date.issued | 2024 | - |
dc.identifier.citation | Plant Journal, 117(2): 616-631 | en_US |
dc.identifier.issn | 0960-7412 | - |
dc.identifier.issn | 1365-313X | - |
dc.identifier.other | https://doi.org/10.1111/tpj.16518 | - |
dc.identifier.uri | https://onlinelibrary.wiley.com/doi/10.1111/tpj.16518 | - |
dc.identifier.uri | http://223.31.159.10:8080/jspui/handle/123456789/1540 | - |
dc.description | Accepted date: 13 October 2023 | en_US |
dc.description.abstract | The 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.sponsorship | The 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.iso | en_US | en_US |
dc.publisher | John Wiley & Sons | en_US |
dc.subject | Sclerotinia sclerotiorum | en_US |
dc.subject | co-immunoprecipitation | en_US |
dc.subject | coronatine induced 1 (CORI3) | en_US |
dc.subject | extra-large Gα protein 2 (XLG2) | en_US |
dc.subject | jasmonic acid | en_US |
dc.subject | plant defense | en_US |
dc.title | XLG2 and CORI3 function additively to regulate plant defense against the necrotrophic pathogen Sclerotinia sclerotiorum | en_US |
dc.type | Article | en_US |
Appears in Collections: | Institutional Publications |
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Bisht NC_2023_4.pdf Restricted Access | 7.94 MB | Adobe PDF | View/Open Request a copy |
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