Abstract

The rhythmic opening/closing and volatile emissions of flowers are known to attract pollinators at specific times. That these rhythms are maintained under constant light or dark conditions suggests a circadian clock involvement. Although a forward and reverse genetic approach has led to the identification of core circadian clock components in Arabidopsis thaliana, the involvement of these clock components in floral rhythms has remained untested, probably because of the weak diurnal rhythms in A.thaliana flowers. Here, we addressed the role of these core clock components in the flowers of the wild tobacco Nicotiana attenuata, whose flowers open at night, emit benzyl acetone (BA) scents and move vertically through a 140° arc. We first measured N.attenuata floral rhythms under constant light conditions. The results suggest that the circadian clock controls flower opening, BA emission and pedicel movement, but not flower closing. We generated transgenic N.attenuata lines silenced in the homologous genes of Arabidopsis LATE ELONGATED HYPOCOTYL (LHY) and ZEITLUPE (ZTL), which are known to be core clock components. Silencing NaLHY and NaZTL strongly altered floral rhythms in different ways, indicating that conserved clock components in N.attenuata coordinate these floral rhythms.

Highlights

  • Linnaeus (1751) designed a garden known as the “flower clock,” comprised of different plant species with unique flower opening and closing times

  • We identified the N. attenuata LATE ELONGATED HYPOCOTYL (LHY) (NaLHY), NaTOC1, and NaZTL, which are the homologous proteins of Arabidopsis LHY, TOC1, and ZTL, respectively (Yon et al, 2012)

  • We showed that the ectopic overexpression of NaLHY and NaZTL in Arabidopsis seedlings results in elongated hypocotyls compared to the hypocotyls of WT seedlings (Yon et al, 2012)

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Summary

Introduction

Linnaeus (1751) designed a garden known as the “flower clock,” comprised of different plant species with unique flower opening and closing times. Cestrum nocturnum (nightblooming jasmine) (Overland, 1960), Nicotiana sylvestris and Nicotiana suaveolens (Loughrin et al, 1991; Kolosova et al, 2001) emit a bouquet of floral scents at night, and Antirrhinum majus (snapdragon) flowers emit methyl benzoate in the afternoon (Kolosova et al, 2001). These famous examples show that flowering plants have characteristic rhythms which synchronize with environmental factors such as the active times of their pollinators (Somers, 1999; Fründ et al, 2011). More recently Montaigu et al (de Montaigu et al, 2014) demonstrated the importance of the day/night cycle transitions for understanding the function of the clock in nature using the Arabidopsis system

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