Abstract

Signaling molecules move between cells to form a characteristic distribution pattern within a developing organ; thereafter, they spatiotemporally regulate organ development. A key question in this process is how the signaling molecules robustly form the precise distribution on a tissue scale in a reproducible manner. Despite of an increasing number of quantitative studies regarding the mobility of signaling molecules, the detail mechanism of organogenesis via intercellular signaling is still unclear. We here review the potential advantages of plant development to address this question, focusing on the cytoplasmic continuity of plant cells through the plasmodesmata. The plant system would provide a unique opportunity to define the simple transportation mode of diffusion process, and, hence, the mechanism of organogenesis via intercellular signaling. Based on the advances in the understanding of intercellular signaling at the molecular level and in the quantitative imaging techniques, we discuss our current challenges in measuring the mobility of signaling molecules for deciphering plant organogenesis.

Highlights

  • A developing organ comprises a heterogeneous field of individual cells that differ in terms of physical conditions, molecular constitution, structures, differentiation stages and other properties

  • The kinetics of intercellular signaling is being investigated in animal development, using quantitative imaging techniques such as fluorescence redistribution after photobleaching (FRAP) and photoconversion of fluorescent proteins

  • We showed recently that the transcriptional co-activator ANGUSTIFOLIA3 (AN3, which is known as GRF-INTERACTING FACTOR1) (Horiguchi et al 2005; Kim and Kende 2004) is produced within mesophyll cells of leaf primordia in Arabidopsis thaliana, and moves into epidermal cells (Kawade et al 2013)

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Summary

Introduction

A developing organ comprises a heterogeneous field of individual cells that differ in terms of physical conditions, molecular constitution, structures, differentiation stages and other properties. To assess the mechanism by which signaling molecules form a tissue-scale gradient distribution through the diffusion process, let us consider a simple one-dimensional mathematical model [Synthesis, Diffusion and Degradation (SDD) model (Crick 1970), Fig. 1].

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