| Literature DB >> 32303662 |
Bianca Ribeiro1,2, Elia Lacchini1,2, Keylla U Bicalho1,2,3, Jan Mertens1,2, Philipp Arendt1,2, Robin Vanden Bossche1,2, Gabriela Calegario1,2, Lore Gryffroy1,2, Evi Ceulemans1,2, Julia Buitink4, Alain Goossens5,2, Jacob Pollier5,2,6.
Abstract
Plants produce a vast array of defense compounds to protect themselves from pathogen attack or herbivore predation. Saponins are a specific class of defense compounds comprising bioactive glycosides with a steroidal or triterpenoid aglycone backbone. The model legume Medicago truncatula synthesizes two types of saponins, hemolytic saponins and nonhemolytic soyasaponins, which accumulate as specific blends in different plant organs. Here, we report the identification of the seed-specific transcription factor TRITERPENE SAPONIN ACTIVATION REGULATOR3 (TSAR3), which controls hemolytic saponin biosynthesis in developing M. truncatula seeds. Analysis of genes that are coexpressed with TSAR3 in transcriptome data sets from developing M. truncatula seeds led to the identification of CYP88A13, a cytochrome P450 that catalyzes the C-16α hydroxylation of medicagenic acid toward zanhic acid, the final oxidation step of the hemolytic saponin biosynthesis branch in M. truncatula In addition, two uridine diphosphate glycosyltransferases, UGT73F18 and UGT73F19, which glucosylate hemolytic sapogenins at the C-3 position, were identified. The genes encoding the identified biosynthetic enzymes are present in clusters of duplicated genes in the M. truncatula genome. This appears to be a common theme among saponin biosynthesis genes, especially glycosyltransferases, and may be the driving force of the metabolic evolution of saponins.Entities:
Mesh:
Substances:
Year: 2020 PMID: 32303662 PMCID: PMC7268793 DOI: 10.1105/tpc.19.00609
Source DB: PubMed Journal: Plant Cell ISSN: 1040-4651 Impact factor: 11.277