Goethe’s seminal scientific work, Versuch die Metamorphose der Pflanzen zu erklaren (An Attempt to Interpret the Metamorphosis of Plants) dated from 1790, has created the foundations for many domains of modern plant biology. The archetypal leaf concept, which considers floral organs as modified leaves, besides being the best known has been proven true, following the description of the ABC molecular model of floral organ identity determination during the last decade. Here we analyze the whole theoretical frame of Goethe’s 1790 publication and present two previously misconsidered aspects of this work: The "refinement of the sap" concept as a directional principle and the "cycles of contractions and expansions" as cycles of differential determination of the shoot apical meristem. The reinterpretation of these concepts are in line with the modern view that molecular networks integrate both environmental and endogenous cues and regulate plant development. This reassessment also helps to elaborate a theoretical frame that considers the evolutionary conservation of the molecular mechanisms that regulate plant development.
In plants the dorsoventral boundary of leaves defines an axis of symmetry through the centre of the organ separating the top (dorsal) and bottom (ventral) tissues. Although the positioning of this boundary is critical for leaf morphogenesis, how the boundary is established and how it influences development remains unclear. Using live-imaging and perturbation experiments we show that leaf orientation, morphology and position are pre-patterned by HD-ZIPIII and KAN gene expression in the shoot, leading to a model in which dorsoventral genes coordinate to regulate plant development by localizing auxin response between their expression domains. However we also find that auxin levels feedback on dorsoventral patterning by spatially organizing HD-ZIPIII and KAN expression in the shoot periphery. By demonstrating that the regulation of these genes by auxin also governs their response to wounds, our results also provide a parsimonious explanation for the influence of wounds on leaf dorsoventrality.
AbstractIn plants the dorsoventral boundary of leaves defines an axis of symmetry through the centre of the organ separating the top (dorsal) and bottom (ventral) tissues. Although the positioning of this boundary is critical for leaf morphogenesis, how the boundary is established and how it influences development remains unclear. Using live-imaging and perturbation experiments we show that leaf orientation, morphology and position are pre-patterned by HD-ZIPIII and KAN gene expression in the shoot, leading to a model in which dorsoventral genes coordinate to regulate plant development by localizing auxin response between their expression domains. However we also find that auxin levels feedback on dorsoventral patterning by spatially organizing HD-ZIPIII and KAN expression in the shoot periphery. By demonstrating that the regulation of these genes by auxin also governs their response to wounds, our results also provide a parsimonious explanation for the influence of wounds on leaf dorsoventrality.
Could animal hormone regulate plant development?
