Structure–Function Relationships of Four Stereoisomers of a Brassinolide Mimetic on Hypocotyl and Root Elongation of the Brassinosteroid-Deficient det2-1 Mutant of Arabidopsis

Abstract

Brassinosteroids (BRs) are a group of plant hormones and the bioactive BR, brassinolide (BL), is causally implicated in promoting cell elongation and cell proliferation. In Arabidopsis, the biosynthesis of BL is essential for hypocotyl etiolation in the dark, and application of bioactive BRs can promote both hypocotyl and root elongation, although high concentrations of applied BRs result in inhibition of root elongation. A non-steroidal structure consisting of four stereoisomers was designed to contain subunits bearing key functional groups mimicking those of BL. The bioactivity of each of these individual stereoisomers was tested using the Arabidopsis thaliana det2-1 mutant line, which is deficient in BL, and thus does not etiolate in the dark. Application of BL at each of 0.1, 1.0, and 10.0 µM promotes hypocotyl elongation in dark-grown det2-1 plants while simultaneously inhibiting elongation of their primary root. In contrast, the mimetic structures, when applied to dark-grown det2-1 plants, promote hypocotyl elongation without negatively affecting primary root elongation. In fact, two of the mimetic structures, applied at a 10 µM concentration, significantly promoted both hypocotyl and root elongation. Correlation of this contrasting behavior with the configurations of the hydroxylated stereocenters of the mimetics is described. This is the first example of a non-steroidal BL mimetic where the biological activities of individual stereoisomers were tested and compared.