Please use this identifier to cite or link to this item: http://223.31.159.10:8080/jspui/handle/123456789/1560
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dc.contributor.authorSingh, Kirti-
dc.contributor.authorSharma, Deepika-
dc.contributor.authorBhagat, Prakash Kumar-
dc.contributor.authorTayyeba, Sumaira-
dc.contributor.authorNoryang, Stanzin-
dc.contributor.authorSinha, Alok Krishna-
dc.date.accessioned2024-01-02T07:06:32Z-
dc.date.available2024-01-02T07:06:32Z-
dc.date.issued2024-
dc.identifier.citationPlant Science, 340: 111967en_US
dc.identifier.issn1873-2259-
dc.identifier.issn0168-9452-
dc.identifier.otherhttps://doi.org/10.1016/j.plantsci.2023.111967-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0168945223003849?via%3Dihub-
dc.identifier.urihttp://223.31.159.10:8080/jspui/handle/123456789/1560-
dc.descriptionAccepted date: 23 December 2023en_US
dc.description.abstractBacterial leaf blight is a devastating disease caused by Xanthomonas oryzae pv. oryzae (Xoo) which causes severe crop loss in rice. The molecular mechanism that initiates defense against such pathogens remains unexplored. Reports have suggested crucial role of several miRNAs in regulating immune responses in plants. Argonaute (AGO) proteins have been implicated in imparting immunity against pathogens by using small RNAs as guide molecules. Here, we show that phosphorylation of rice AGO1a by MAP kinases is required for miRNA expression regulation during Xoo infection. AGO1a is induced in response to pathogen infection and is under the control of SA signaling pathway. The pathogen responsive MAP kinases MPK3, MPK4 and MPK6, interact with AGO1a in planta and can phosphorylate the protein in vitro. Overexpression of AGO1a extends disease resistance against Xoo in rice and leads to a higher accumulation of miRNAs. Conversely, overexpression of a non phosphorylatable mutant protein aggravates disease susceptibility and remarkably suppresses the miRNA expression levels. At a molecular level, phosphorylation of AGO1a by MAP kinase is required for increased accumulation of miRNAs during pathogen challenge. Taken together, the data suggests that OsAGO1a is a direct phosphorylation target of MAP kinases and this phosphorylation is crucial for its role in imparting disease resistance.en_US
dc.description.sponsorshipK.S. received fellowship from Council of Scientific and Industrial Research (CSIR), Govt. of India. P.K.B. was a recipient of a fellowship from Department of Biotechnology (DBT), Government of India. S.T. and S.N. were recipients of fellowships from the University Grant Commission (UGC), Government of India. D.S. acknowledges Department of Science and Technology (DST), Government of India for DST-INSPIRE fellowship. A.K.S. acknowledges Sir J.C. Bose National Fellowship Award Grant from Science and Engineering Research Board (SERB), Government of India. Authors thank the Radioisotope facility, Confocal Microscopy Facility, GFAPC Facility and the Central Instrumentation Facility of NIPGR, New Delhi, India. The authors are thankful to DBT-eLibrary Consortium (DeLCON) for providing access to e-resources.en_US
dc.language.isoen_USen_US
dc.publisherElsevier B.V.en_US
dc.subjectmiRNAen_US
dc.subjectAGO1aen_US
dc.subjectMAP kinaseen_US
dc.subjectXanthomonas oryzaeen_US
dc.subjectgene regulationen_US
dc.subjectbiotic stressen_US
dc.subjectphosphorylationen_US
dc.titlePhosphorylation of AGO1a by MAP kinases is required for miRNA mediated resistance against Xanthomonas oryzae pv. oryzae infection in riceen_US
dc.typeArticleen_US
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