Phytohormone inhibitor treatments phenocopy brassinosteroid and gibberellin dwarf mutant interactions in maize

Phytohormone biosynthesis produces metabolites with profound effects on plant growth and development. Modulation of hormone levels during developmental events, in response to the environment, by genetic polymorphism, or by chemical application can reveal the plant processes most responsive to a phytohormone. In many cases, chemical inhibitors are applied and the levels of specific phytohormones are measured to determine if, and which, phytohormone is affected by a molecule. In many cases, the sensitivity of biochemical testing has determined multiple pathways affected by a single inhibitor. Genetic studies are not subject to this problem, and a wealth of data about the morphological impacts of hormone biosynthetic inhibition has accumulated through the study of enzyme mutants. We previously identified a complex interplay between brassinosteroid (BR) and gibberellin (GA) in maize, where the interdependence of the two differs dependent on the developmental context. We found that: GA is required for loss of BR to induce retained pistils in the tassel florets (POPIT); BR is required for the loss of GA to induce tiller outgrowth; BR and GA are additive for plant height; BR has no effect on the induction of anther retention in ear florets of GA mutants. In this work, we sought to assess the specificity of three triazole inhibitors of cytochrome P450s by determining their abilities to recapitulate the phenotype of double mutants. The GA biosynthetic inhibitors uniconazole (UCZ) and paclobutrazol (PAC) were applied to the BR biosynthetic mutant and all double mutant phenotypes were recovered in the UCZ treatment. PAC was unable to suppress the retention of pistils in the tassels of () mutant plants. The BR biosynthetic inhibitor propiconazole (PCZ) suppressed tiller outgrowth in the GA biosynthetic mutant (). All treatments were additive with genetic mutants for effects on plant height. Due to additional measurements done here but not in previous studies of the double mutants, we detected new interactions between GA and BR biosynthesis affecting plastochron index and tassel branching. These experiments, a refinement of our previous model, and a discussion of the extension of this type of work are presented.