Modulation of expression of miR858 and target genes and metabolite accumulation on supplementation with truncated peptide. A) Quantification of miR858a and its target genes MYB12 and CHS in 5-d-old seedlings of WT grown on half-strength MS medium supplemented with water and miPEP858CR lines supplemented with water (control) and 0.25 µM of truncated peptides 2H and 3F. B) Western blot analysis of MYB12 and CHS protein in 5-d-old WT seedlings grown on half-strength MS medium supplemented with water and miPEP858CR lines supplemented with water (control) and 0.25 µM of 2H, 3F, and miPEP858a. Actin was used as the loading control. C) Quantification of lignin in 35-d-old stems of WT plants supplemented with water and miPEP858CR lines supplemented with water (control) and 0.25 µM of 2H, 3F, and miPEP858a. The experiments were repeated 3 times independently, with similar results. D) Lengths of vascular bundles of 35-d-old stems of WT plants supplemented with water and miPEP858CR lines supplemented with water (control) and 0.25 µM of 2H, 3F, and miPEP858a (n = 15). E) Lengths of interfascicular fibers of 35-d-old stems of WT plants supplemented with water and miPEP858CR lines supplemented with water (control) and 0.25 µM of 2H, 3F, and miPEP858a (n = 15). F) Quantification of total flavonol in 10-d-old WT seedling grown on half-strength MS medium supplemented with water and miPEP858CR lines supplemented with water (control) and 0.25 µM of 0.25 µM of 2H, 3F, and miPEP858a. FW, fresh weight. G) Quantification of anthocyanin in 10-d-old WT seedlings grown on half-strength MS medium supplemented with water and miPEP858CR lines supplemented with water (control) and 0.25 µM of 0.25 µM of 2H, 3F, and miPEP858a. FW, fresh weight.
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