Flavonols affect the interrelated glucosinolate and camalexin biosynthetic pathways in Arabidopsis thaliana

Jogindra Naik, Shivi Tyagi, Ruchika Rajput, Pawan Kumar, Boas Pucker, Naveen C. Bisht, Prashant Misra, Ralf Stracke, Ashutosh Pandey

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

Flavonols are structurally and functionally diverse biomolecules involved in plant biotic and abiotic stress tolerance, pollen development, and inhibition of auxin transport. However, their effects on global gene expression and signaling pathways are unclear. To explore the roles of flavonol metabolites in signaling, we performed comparative transcriptome and targeted metabolite profiling of seedlings from the flavonol-deficient Arabidopsis loss-of-function mutant flavonol synthase1 (fls1) with and without exogenous supplementation of flavonol derivatives (kaempferol, quercetin, and rutin). RNA-seq results indicated that flavonols modulate various biological and metabolic pathways, with significant alterations in camalexin and aliphatic glucosinolate synthesis. Flavonols negatively regulated camalexin biosynthesis but appeared to promote the accumulation of aliphatic glucosinolates via transcription factor-mediated up-regulation of biosynthesis genes. Interestingly, upstream amino acid biosynthesis genes involved in methionine and tryptophan synthesis were altered under flavonol deficiency and exogenous supplementation. Quercetin treatment significantly up-regulated aliphatic glucosinolate biosynthesis genes compared with kaempferol and rutin. In addition, expression and metabolite analysis of the transparent testa7 mutant, which lacks hydroxylated flavonol derivatives, clarified the role of quercetin in the glucosinolate biosynthesis pathway. This study elucidates the molecular mechanisms by which flavonols interfere with signaling pathways, their molecular targets, and the multiple biological activities of flavonols in plants.

Original languageEnglish
Pages (from-to)219-240
Number of pages22
JournalJournal of Experimental Botany
Volume75
Issue number1
DOIs
StatePublished - Jan 1 2024

Funding

JN and RR acknowledge the Council of Scientific and Industrial Research and the Government of India for Senior Research Fellowships. ST acknowledges the Department of Biotechnology, for a Research Associate (RA) Fellowship. The authors thank the DBT-eLibrary Consortium (DeLCON) for providing access to e-resources. We thank Christoph Ringli, University of Zurich, for providing the A. thaliana fls1-3 mutant. We acknowledge the Metabolome facility (BT/INF/22/SP28268/2018) at the NIPGR for the phytochemical analysis. Many thanks to the German Network for Bioinformatics Infrastructure (de.NBI, grant 031A533A) and the Bioinformatics Resource Facility (BRF) at the Center for Biotechnology (CeBiTec) at Bielefeld University for providing the environment to perform the computational analyses. This work was supported by a core grant from the National Institute of Plant Genome Research (NIPGR) and a Department of Biotechnology grant (BT/PR/38402/GET/119/308/2020) to AP.

Keywords

  • Arabidopsis thaliana
  • camalexin
  • flavonol synthase
  • flavonols
  • glucosinolate
  • metabolites
  • reactive oxygen species
  • transparent testa 7

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