Abstract

Floral meristems are dynamic systems that generate floral organ primordia at their flanks and, in most species, terminate while giving rise to the gynoecium primordia. However, we find species with floral meristems that generate additional ring meristems repeatedly throughout angiosperm history. Ring meristems produce only stamen primordia, resulting in polystemous flowers (having stamen numbers more than double that of petals or sepals), and act independently of the floral meristem activity. Most of our knowledge on floral meristem regulation is derived from molecular genetic studies of Arabidopsis thaliana, a species with a fixed number of floral organs and, as such of only limited value for understanding ring meristem function, regulation, and ecological value. This review provides an overview of the main molecular players regulating floral meristem activity in A. thaliana and summarizes our knowledge of ring primordia morphology and occurrence in dicots. Our work provides a first step toward understanding the significance and molecular genetics of ring meristem regulation and evolution.

Highlights

  • Plants 2021, 10, 1140. https://doi.org/Flowers are among the most beautiful examples of mutually beneficial relationships between animals and plants

  • Our work provides a first step toward understanding the significance and molecular genetics of ring meristem regulation and evolution

  • We compiled recent findings on transcription factors, signaling pathways, and phytohormone action, all involved in floral meristem termination of Arabidopsis

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Summary

Introduction

Flowers are among the most beautiful examples of mutually beneficial relationships between animals and plants. In Arabidopsis thaliana, all floral organs arise from the floral meristem which, unlike the shoot or root meristem, undergoes a genetically defined succession of initiation, maintenance, and termination such that stem cell activity ceases once all floral organs are formed [5]. Arabidopsis thaliana has a fixed number of floral organs and is typical for the canalized floral ground plan of many core eudicots Deviations from this ground plan are numerous, and little is known about the conservation of the gene regulatory network (GRN) balancing floral meristem action. While it seems reasonable to assume that some degree of conservation exists in floral meristem GRNs, this genetic system allows extreme examples of variation of floral organ number (merosity), the floral meristem of the Ranunculaceae Laccopetalum giganteum generates up to 10,000 small carpels [13], while the bisexual Hydatellaceae (sister to all other Nymphaeales) flowers consist of either a single stamen or a single carpel [14]

Regulation of Stem Cell Activity in the Floral Meristem
How to Generate Multiple Stamen Primordia
Ring Meristems in Eudicots
Are Ring Meristems in Dicots of Independent Origin?
Conclusions and Outlook
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