Please use this identifier to cite or link to this item: http://223.31.159.10:8080/jspui/handle/123456789/1092
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dc.contributor.authorKumar, Rajiv-
dc.contributor.authorBarua, Pragya-
dc.contributor.authorChakraborty, Niranjan-
dc.contributor.authorNandi, Ashis Kumar-
dc.date.accessioned2020-09-07T10:15:50Z-
dc.date.available2020-09-07T10:15:50Z-
dc.date.issued2020-
dc.identifier.citationPlant Cell Reports, 39: 1549–1563en_US
dc.identifier.issn1432-203X-
dc.identifier.otherhttps://doi.org/10.1007/s00299-020-02583-3-
dc.identifier.urihttps://link.springer.com/article/10.1007/s00299-020-02583-3-
dc.identifier.urihttp://223.31.159.10:8080/jspui/handle/123456789/1092-
dc.descriptionAccepted date: 20 August 2020en_US
dc.description.abstractKey message A comparative proteomic study between WT and SAR-compromised rsi1/fd mutant reveals a set of proteins having possible roles in the SAR development. Abstract A partly infected plant shows enhanced resistance during subsequent infection through the development of systemic acquired resistance (SAR). Mobile signals generated at the site of primary infection travel across the plant for the activation of SAR. These mobile signals are likely to cause changes in the expression of a set of proteins in the distal tissue, which contributes to the SAR development. However, SAR-specifc proteome is not revealed for any plant. The reduced systemic immunity 1 (rsi1)/(allelic to fowering locus D; fd) mutant of Arabidopsis is compromised for SAR but shows normal local resistance. Here we report the SAR-specifc proteome of Arabidopsis by comparing diferentially abundant proteins (DAPs) between WT and fd mutant. Plants were either mock-treated or SAR-induced by primary pathogen inoculation. For proteomic analysis, samples were collected from the systemic tissues before and after the secondary inoculation. Protein identifcation was carried out by using two-dimensional gel electrophoresis (2-DE) followed by tandem mass spectrometry. Our work identifed a total of 94 DAPs between mock and pathogen treatment in WT and fd mutant. The DAPs were categorized into diferent functional groups along with their subcellular localization. The majority of DAPs are involved in metabolic processes and stress response. Among the subcellular compartments, plastids contained the highest number of DAPs, suggesting the importance of plastidic proteins in SAR activation. The fndings of this study would provide resources to engineer efcient SAR activation traits in Arabidopsis and other plants.en_US
dc.description.sponsorshipThis work was supported by the DBT grant (No. BT/PR23632/BPA/118/312/2017) to AKN and D.S. Kothari post-doctoral fellowship (No. F.4-2/2006 (BSR)/BL/13-14/0456) to RK.en_US
dc.language.isoen_USen_US
dc.publisherSpringer Nature Publishing AGen_US
dc.subjectComparative proteomic analysisen_US
dc.subjectDiferentially abundant proteinsen_US
dc.subjectflden_US
dc.subjectPlant immunityen_US
dc.subjectrsi1en_US
dc.subjectSystemic acquired resistanceen_US
dc.titleSystemic acquired resistance specifc proteome of Arabidopsis thalianaen_US
dc.typeArticleen_US
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