Abstract

Plants have the ability to continously generate new organs by maintaining populations of stem cells throught their lives. The shoot apical meristem (SAM) provides a stable environment for the maintenance of stem cells. All cells inside the SAM divide, yet boundaries and patterns are maintained. Experimental evidence indicates that patterning is independent of cell lineage, thus a dynamic self-regulatory mechanism is required. A pivotal role in the organization of the SAM is played by the WUSCHEL gene (WUS). An important question in this regard is that how WUS expression is positioned in the SAM via a cell-lineage independent signaling mechanism. In this study we demonstrate via mathematical modeling that a combination of an inhibitor of the Cytokinin (CK) receptor, Arabidopsis histidine kinase 4 (AHK4) and two morphogens originating from the top cell layer, can plausibly account for the cell lineage-independent centering of WUS expression within SAM. Furthermore, our laser ablation and microsurgical experiments support the hypothesis that patterning in SAM occurs at the level of CK reception and signaling. The model suggests that the interplay between CK signaling, WUS/CLV feedback loop and boundary signals can account for positioning of the WUS expression, and provides directions for further experimental investigation.

Highlights

  • All the aerial plant parts are generated by the shoot apical meristem (SAM) situated at the plant apex

  • For simplicity, we assume that the dynamics of the WUSCHEL gene (WUS)/CLV3 regulatory system arising from the assumed reaction-diffusion system are sufficiently faster than the cell division rate in the SAM

  • In order to compensate for the lack of supply of CK via the stem and to aid the WUS is a major component of SAM development and stem cell homeostasis

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Summary

Introduction

All the aerial plant parts are generated by the shoot apical meristem (SAM) situated at the plant apex. The SAM is formed during embryogenesis and in dicotyledonous angiosperms, such as the model plant Arabidopsis thaliana, it contains three layers of stem cells in the three outermost cell layers [1, 2]. Clonal studies indicate that each layer contains about three long lived stem cells [3] in the central zone (CZ), which is marked by a lower cell division rate. Positioning the Organizing Center in Arabidopsis Meristem. Daughter cells of the stem cells that stay in the CZ replenish the stem cell pool, whereas daughter cells that are placed towards the peripheral zone (PZ), which is marked by a higher cell division rate, enter differentiation and form organ primordia. The shape and the domain structure of the SAM are kept unchanged, all cells continuously divide and differentiating stem cell daughters leave the meristem. Due to its changing cellular context, pattern formation of the shoot meristem does not rely on a stable point of reference, but rather occurs in a self organized manner [1]

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