Abstract

Flowering time is strictly controlled by a combination of internal and external signals that match seed set with favorable environmental conditions. In the model plant species Arabidopsis thaliana (Brassicaceae), many of the genes underlying development and evolution of flowering have been discovered. However, much remains unknown about how conserved the flowering gene networks are in plants with different growth habits, gene duplication histories, and distributions. Here we functionally characterize three homologs of the flowering gene SUPPRESSOR OF OVEREXPRESSION OF CONSTANS 1 (SOC1) in the short-lived perennial Petunia hybrida (petunia, Solanaceae). Similar to A. thaliana soc1 mutants, co-silencing of duplicated petunia SOC1-like genes results in late flowering. This phenotype is most severe when all three SOC1-like genes are silenced. Furthermore, expression levels of the SOC1-like genes UNSHAVEN (UNS) and FLORAL BINDING PROTEIN 21 (FBP21), but not FBP28, are positively correlated with developmental age. In contrast to A. thaliana, petunia SOC1-like gene expression did not increase with longer photoperiods, and FBP28 transcripts were actually more abundant under short days. Despite evidence of functional redundancy, differential spatio-temporal expression data suggest that SOC1-like genes might fine-tune petunia flowering in response to photoperiod and developmental stage. This likely resulted from modification of SOC1-like gene regulatory elements following recent duplication, and is a possible mechanism to ensure flowering under both inductive and non-inductive photoperiods.

Highlights

  • Flowering time is a complex trait shaped by internal and external signals that interplay to determine reproductive success [1,2]

  • FLOWERING LOCUS T (FT) protein is translocated through the phloem to the shoot apical meristem (SAM) where it binds with FLOWERING LOCUS D (FD) to induce the expression of floral promoters such as SUPPRESSOR OF OVEREXPRESSION OF CONSTANS 1 (SOC1), APETALA1 (AP1), FRUITFULL (FUL), and LEAFY (LFY) [6,7,8]

  • Infiltration of petunia seedlings with Agrobacterium resulted in a total of 24, 21, 37, and 4 plants positive for the CHALCONE SYNTHASE (CHS), FLORAL BINDING PROTEIN 21 (FBP21), FBP28, and FBP21/28-tobacco rattle virus 2 (TRV2) constructs, respectively (Fig. 2A)

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Summary

Introduction

Flowering time is a complex trait shaped by internal and external signals that interplay to determine reproductive success [1,2]. Flowering time pathways have evolved to both respond to, and buffer against, environmental variation. These seemingly opposing forces can be achieved either by integrating signals from parallel genetic pathways or by differentially utilizing related genes within the same pathway. In the annual rosid species Arabidopsis thaliana (Brassicaceae) long day induced flowering is controlled by CONSTANS (CO)mediated upregulation of the integrator protein FLOWERING LOCUS T (FT) in leaves [3,4,5]. Largely functionally conserved across both long and short day-induced flowering plants [9,10,11]

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