| Literature DB >> 35788779 |
Evandro Alexandre Fortini1, Diego Silva Batista2, Sérgio Heitor Sousa Felipe3, Tatiane Dulcineia Silva1, Ludmila Nayara Freitas Correia1, Letícia Monteiro Farias4, Daniele Vidal Faria1, Vitor Batista Pinto5, Claudete Santa-Catarina6, Vanildo Silveira5, Clelia De-la-Peña7, Eduardo Castillo-Castro7, Wagner Campos Otoni8.
Abstract
Plants adjust their complex molecular, biochemical, and metabolic processes to overcome salt stress. Here, we investigated the proteomic and epigenetic alterations involved in the morphophysiological responses of Pfaffia glomerata, a medicinal plant, to salt stress and the demethylating agent 5-azacytidine (5-azaC). Moreover, we investigated how these changes affected the biosynthesis of 20-hydroxyecdysone (20-E), a pharmacologically important specialized metabolite. Plants were cultivated in vitro for 40 days in Murashige and Skoog medium supplemented with NaCl (50 mM), 5-azaC (25 μM), and NaCl + 5-azaC. Compared with the control (medium only), the treatments reduced growth, photosynthetic rates, and photosynthetic pigment content, with increase in sucrose, total amino acids, and proline contents, but a reduction in starch and protein. Comparative proteomic analysis revealed 282 common differentially accumulated proteins involved in 87 metabolic pathways, most of them related to amino acid and carbohydrate metabolism, and specialized metabolism. 5-azaC and NaCl + 5-azaC lowered global DNA methylation levels and 20-E content, suggesting that 20-E biosynthesis may be regulated by epigenetic mechanisms. Moreover, downregulation of a key protein in jasmonate biosynthesis indicates the fundamental role of this hormone in the 20-E biosynthesis. Taken together, our results highlight possible regulatory proteins and epigenetic changes related to salt stress tolerance and 20-E biosynthesis in P. glomerata, paving the way for future studies of the mechanisms involved in this regulation.Entities:
Keywords: Abiotic stress; DNA methylation; Medicinal plant; Methyltransferase inhibitor; Phytoecdysteroids; Proteomics
Year: 2022 PMID: 35788779 DOI: 10.1007/s00709-022-01789-4
Source DB: PubMed Journal: Protoplasma ISSN: 0033-183X Impact factor: 3.356