Abstract

The phytohormone auxin is implied in steering various developmental decisions during plant morphogenesis in a concentration-dependent manner. Auxin maxima have been shown to maintain meristematic activity, for example, of the root apical meristem, and position new sites of outgrowth, such as during lateral root initiation and phyllotaxis. More recently, it has been demonstrated that sites of auxin minima also provide positional information. In the developing Arabidopsis fruit, auxin minima are required for correct differentiation of the valve margin. It remains unclear, however, how this auxin minimum is generated and maintained. Here, we employ a systems biology approach to model auxin transport based on experimental observations. This allows us to determine the minimal requirements for its establishment. Our simulations reveal that two alternative processes—which we coin “flux-barrier” and “flux-passage”—are both able to generate an auxin minimum, but under different parameter settings. Both models are in principle able to yield similar auxin profiles but present qualitatively distinct patterns of auxin flux. The models were tested by tissue-specific inducible ablation, revealing that the auxin minimum in the fruit is most likely generated by a flux-passage process. Model predictions were further supported through 3D PIN localization imaging and implementing experimentally observed transporter localization. Through such an experimental–modeling cycle, we predict how the auxin minimum gradually matures during fruit development to ensure timely fruit opening and seed dispersal.

Highlights

  • Patterning through morphogens is considered one of the first triggers for correct tissue differentiation (Raspopovic et al, 2014; Wolpert, 2016)

  • Flower and fruit development in Arabidopsis thaliana has been intensely studied over decades

  • We took into account transport across cell membranes due to background influx and very low efflux permeability rates, together with augmented influx and efflux contributed by the AUX1/LAXs and PINs

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Summary

Introduction

Patterning through morphogens is considered one of the first triggers for correct tissue differentiation (Raspopovic et al, 2014; Wolpert, 2016). Cell differentiation hinges on the concept of genetic control, first elucidated for single cells by the pioneering work of Jacques Monod, an early advocate of a systems view of living cells (Ullmann, 2011). How the patterning of cell differentiation is controlled within a coordinated multicellular structure, leads us to go beyond ‘‘anything found to be true of E. coli must be true of elephants, only more so’’ (Jacob and Philip, 1995). Tissue fates and their progressive differentiation are steered by phytohormones and their downstream genetic targets

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