Secoiridoids Metabolism Response to Wounding in Common Centaury (Centaurium erythraea Rafn) Leaves.
Jelena BožunovićMarijana SkorićDragana MatekaloSuzana ŽivkovićMilan DragićevićNeda AničićBiljana K FilipovićTijana BanjanacBranislav ŠilerDanijela M MišićPublished in: Plants (Basel, Switzerland) (2019)
Centaurium erythraea Rafn produces and accumulates various biologically active specialized metabolites, including secoiridoid glucosides (SGs), which help plants to cope with unfavorable environmental conditions. Specialized metabolism is commonly modulated in a way to increase the level of protective metabolites, such as SGs. Here, we report the molecular background of the wounding-induced changes in SGs metabolism for the first time. The mechanical wounding of leaves leads to a coordinated up-regulation of SGs biosynthetic genes and corresponding JA-related transcription factors (TFs) after 24 h, which results in the increase of metabolic flux through the biosynthetic pathway and, finally, leads to the elevated accumulation of SGs 96 h upon injury. The most pronounced increase in relative expression was detected for secologanin synthase (CeSLS), highlighting this enzyme as an important point for the regulation of biosynthetic flux through the SG pathway. A similar expression pattern was observed for CeBIS1, imposing itself as the TF that is prominently involved in wound-induced regulation of SGs biosynthesis genes. The high degree of positive correlations between and among the biosynthetic genes and targeted TFs expressions indicate the transcriptional regulation of SGs biosynthesis in response to wounding with a significant role of CeBIS1, which is a known component of the jasmonic acid (JA) signaling pathway.
Keyphrases
- poor prognosis
- signaling pathway
- genome wide
- genome wide identification
- transcription factor
- ms ms
- palliative care
- bioinformatics analysis
- pi k akt
- binding protein
- drug induced
- long non coding rna
- gene expression
- cell proliferation
- oxidative stress
- cancer therapy
- diabetic rats
- drug delivery
- cell wall
- single molecule
- endoplasmic reticulum stress