Please use this identifier to cite or link to this item: http://223.31.159.10:8080/jspui/handle/123456789/1795
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dc.contributor.authorJogawat, Abhimanyu-
dc.contributor.authorSanyasi, Madhan-
dc.contributor.authorMenon, Sidhardh H-
dc.contributor.authorGoyal, Divya-
dc.contributor.authorNair, Athira Mohandas-
dc.contributor.authorVadassery, Jyothilakshmi-
dc.date.accessioned2026-03-17T06:09:46Z-
dc.date.available2026-03-17T06:09:46Z-
dc.date.issued2026-
dc.identifier.citationPlant and Cell Physiology, (In Press)en_US
dc.identifier.issn1471-9053-
dc.identifier.otherhttps://doi.org/10.1093/pcp/pcag032-
dc.identifier.urihttps://academic.oup.com/pcp/advance-article/doi/10.1093/pcp/pcag032/8516506?login=true-
dc.identifier.urihttp://223.31.159.10:8080/jspui/handle/123456789/1795-
dc.descriptionAccepted date: 01 March 2026en_US
dc.description.abstractCarbon availability is a central determinant of beneficial plant–fungal associations, and sugar transporters are key levers of this exchange. SWEETs (SUGARS WILL EVENTUALLY BE EXPORTED TRANSPORTER) are involved in transporting various kinds of sugars in plants; however, their functional roles in fungal symbiosis are not sufficiently explored. In this study, we investigate the functional relevance of Arabidopsis SWEETs in the interaction with endophytic fungi, Serendipita indica. Transcript profiling of SWEET genes in response to S. indica and its major elicitor, cellotriose, revealed early root-specific induction of SWEET12. Using a SWEET12 loss-of-function mutant, we demonstrate that the absence of SWEET12 disrupts the major outcomes of mutualism including growth promotion, balanced colonization, sugar allocation, and the accumulation of defense phytohormones (JA and SA). Transcriptome profiling further reveals that SWEET12 buffers whole-plant responses by coordinating genes linked to carbohydrate, nitrogen, and lipid metabolism, and by tuning defense signalling and nutrient transporter networks. Our findings indicate that SWEET12 is essential for balancing fungal colonization and host defense, thereby promoting plant growth. SWEET12 does so by acting as sugar valve that meters sugar release to the apoplast, enabling the fungus to access carbon while preserving host sugar homeostasis and immune competence.en_US
dc.description.sponsorshipThis work was supported by Department of Biotechnology, Government of India for providing fellowship and research funding through MK Bhan-Young Researcher Fellowship (File No. HRD-16016/2/2023-AFS-DBT) program to AJ. MS and SHM were funded by JRF from MK Bhan-Young Researcher Fellowship of AJ. AMN acknowledges DSTINSPIRE fellowship. We acknowledge NIPGR for core grant, Central instrumentation Facility, Metabolome Facility. We thank Senthil-Kumar Muthappa (NIPGR) for providing mutant of SWEET12. We thank Cécile Vriet (University of Poitiers) for gifting GUS line of SWEET12. We also acknowledge Neuberg Supratech Laboratories, Ahmadabad, India for RNA sequencing.en_US
dc.language.isoen_USen_US
dc.publisherOxford University Pressen_US
dc.subjectSerendipita indicaen_US
dc.subjectSWEET12en_US
dc.subjectfungal symbiosisen_US
dc.subjectroot transcriptomeen_US
dc.subjectsugarsen_US
dc.titleArabidopsis SWEET12 contributes to the regulation of sugar allocation and defense responses during interaction with Serendipita indicaen_US
dc.typeArticleen_US
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