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Systems Biology Approach Pinpoints Minimum Requirements for Auxin Distribution during Fruit Opening.

Authors :
Li, Xin-Ran
Vroomans, Renske M.A.
Fox, Samantha
Grieneisen, Verônica A.
Østergaard, Lars
Marée, Athanasius F.M.
Source :
Molecular Plant (Cell Press). Jun2019, Vol. 12 Issue 6, p863-878. 16p.
Publication Year :
2019

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. We investigate the mechanism leading to a spatially confined auxin minimum required for Arabidopsis fruit opening and seed dispersal. Our experiment–modeling cycle reveals a counterintuitive mechanism of its formation: efflux activity creates an auxin minimum strip that is accompanied by high auxin fluxes crossing it perpendicularly. This dynamical process can be associated with the maturation of the fruit. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16742052
Volume :
12
Issue :
6
Database :
Academic Search Index
Journal :
Molecular Plant (Cell Press)
Publication Type :
Academic Journal
Accession number :
136729745
Full Text :
https://doi.org/10.1016/j.molp.2019.05.003