Please use this identifier to cite or link to this item: http://223.31.159.10:8080/jspui/handle/123456789/1172
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dc.contributor.authorNaik, Jogindra-
dc.contributor.authorRajput, Ruchika-
dc.contributor.authorPucker, Boas-
dc.contributor.authorStracke, Ralf-
dc.contributor.authorPandey, Ashutosh-
dc.date.accessioned2021-03-17T07:09:47Z-
dc.date.available2021-03-17T07:09:47Z-
dc.date.issued2021-
dc.identifier.citationPlant Molecular Biology, (In Press)en_US
dc.identifier.issn1573-5028-
dc.identifier.otherhttps://doi.org/10.1007/s11103-021-01135-x-
dc.identifier.urihttps://link.springer.com/article/10.1007/s11103-021-01135-x-
dc.identifier.urihttp://223.31.159.10:8080/jspui/handle/123456789/1172-
dc.descriptionAccepted: 25 February 2021en_US
dc.description.abstractFlavonols are plant specialized metabolites with vital roles in plant development and defense and are known as diet compound beneficial to human health. In leguminous plants, the regulatory proteins involved in flavonol biosynthesis are not well characterized. Using a homology-based approach, three R2R3-MYB transcription factor encoding genes have been identified in the Medicago truncatula reference genome sequence. The gene encoding a protein with highest similarity to known flavonol regulators, MtMYB134, was chosen for further experiments and was characterized as a functional flavonol regulator from M. truncatula. MtMYB134 expression levels are correlated with the expression of MtFLS2, encoding a key enzyme of flavonol biosynthesis, and with flavonol metabolite content. MtMYB134 was shown to activate the promoters of the A. thaliana flavonol biosynthesis genes AtCHS and AtFLS1 in Arabidopsis protoplasts in a transactivation assay and to interact with the Medicago promoters of MtCHS2 and MtFLS2 in yeast 1-hybrid assays. To ascertain the functional aspect of the identified transcription factor, we developed a sextuple mutant, which is defective in anthocyanin and flavonol biosynthesis. Ectopic expression of MtMYB134 in a multiple myb A. thaliana mutant restored flavonol biosynthesis. Furthermore, overexpression of MtMYB134 in hairy roots of M. truncatula enhanced the biosynthesis of various flavonol derivatives. Taken together, our results provide insight into the understanding of flavonol biosynthesis regulation in M. truncatula and provides MtMYB134 as tool for genetic manipulation to improve flavonol synthesis.en_US
dc.description.sponsorshipWe are thankful to Dr. Senjuti Sinha Roy for providing Medicago truncatula seeds. This work was supported by the core grant of National Institute of Plant Genome Research and Department of Science and Technology-SERB for Startup research grant to AP (Grant Number: SRG/2019/000503). JN and Ruchika acknowledge Council of Scientifc and Industrial Research, Government of India for Senior Research Fellowships. The authors are thankful to DBTeLibrary Consortium (DeLCON) for providing access to e-resources. We acknowledge Metabolome facility (BT/ INF/22/SP28268/2018) at NIPGR for phytochemical analysis.en_US
dc.language.isoen_USen_US
dc.publisherSpringer Nature Publishing AGen_US
dc.subjectMetabolic engineeringen_US
dc.subjectLegumeen_US
dc.subjectGene expression analysisen_US
dc.subjectHairy root transformationen_US
dc.subjectFlavonol biosynthesisen_US
dc.titleThe R2R3‑MYB transcription factor MtMYB134 orchestrates favonol biosynthesis in Medicago truncatulaen_US
dc.typeArticleen_US
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