Interaction of ToLCNDV TrAP with SlATG8f marks it susceptible to degradation by autophagy

dc.contributor.authorPrasad, Ashish
dc.contributor.authorPrasad, Manoj
dc.date.accessioned2022-04-19T09:21:04Z
dc.date.available2022-04-19T09:21:04Z
dc.date.issued2022
dc.descriptionAccepted date: 30 March 2022en_US
dc.description.abstractTomato leaf curl New Delhi virus (ToLCNDV) is a devastating plant pathogen which causes significant losses in tomato yield. According to previous reports, proteins of geminiviruses like βC1 of Cotton leaf curl Multan virus and C1 of Tomato leaf curl Yunnan virus are degraded by the autophagy pathway. There are no reports on the role of autophagy in ToLCNDV pathogenesis. In this study, we have shown that SlATG8f interacts with the ToLCNDV Transcription activator protein (TrAP; AC2) to mediate its degradation by the autophagy pathway. Silencing of SlATG8f in a ToLCNDV tolerant tomato cultivar; H-88-78-1 resulted in enhanced viral symptoms and ToLCNDV accumulation suggesting an anti-viral role for SlATG8f against ToLCNDV. TrAP is a nucleus localized protein, but it interacts with SlATG8f in and outside the nucleus indicating its nuclear export. This export might be mediated by Exportin1 as treatment with Exportin1 inhibitor inhibits TrAP export outside the nucleus. ToLCNDV TrAP is known to possess host RNA silencing suppression (RSS) activity. Degradation of TrAP results in the attenuation of its RSS activity. To the best of our knowledge, we have shown for the first time that SlATG8f-TrAP interaction leads to TrAP degradation providing defence against ToLCNDV.en_US
dc.description.sponsorshipWe thank Dr. Sunil Mukherjee (IARI, New Delhi), Dr. Namisha Sharma (NIPGR, New Delhi) and Mrs. Shambhavi Sharma (NIPGR, New Delhi) for critically reading the manuscript. We thank Prof. Savithramma Dinesh-Kumar, Plant Biology Department, University of California, Davis, USA for providing TRV-based VIGS vectors. We thank DBT-eLibrary Consortium (DeLCON) for providing access to e-resources. Figure 4D was created with BioRender.com. This work was supported by projects from Ministry of Science and Technology, Govt. of India [Department of Biotechnology [BT/PR/38399/GET/119/307/2020 and JC Bose Fellowship JCB/2018/000001] to M.P. Research fellowship from Council of Scientific and Industrial Research, Govt. of India to A.P.en_US
dc.identifier.citationCellular and Molecular Life Sciences, 79(5): 241en_US
dc.identifier.issn1420-9071
dc.identifier.issn1420-682X
dc.identifier.otherhttps://doi.org/10.1007/s00018-022-04281-7
dc.identifier.urihttps://link.springer.com/article/10.1007/s00018-022-04281-7
dc.identifier.urihttps://ndkr-library.nipgr.ac.in/handle/123456789/1326
dc.language.isoen_USen_US
dc.publisherSpringer Nature Publishing AGen_US
dc.subjectAutophagyen_US
dc.subjectPlant defenceen_US
dc.subjectRNA silencing suppressoren_US
dc.subjectSlATG8fen_US
dc.subjectToLCNDVen_US
dc.subjectTranscriptional activator proteinen_US
dc.titleInteraction of ToLCNDV TrAP with SlATG8f marks it susceptible to degradation by autophagyen_US
dc.typeArticleen_US

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