Abstract

Appropriate control of flowering time is crucial for crop yield and the reproductive success of plants. Flowering can be induced by a number of molecular pathways that respond to internal and external signals. In Arabidopsis, expression of the key florigenic signal FLOWERING LOCUS T (FT) is positively regulated by CONSTANS (CO) a BBX protein sharing high sequence similarity with 16 CO-like proteins. Within this study, we investigated the role of the Arabidopsis CONSTANS-LIKE 4 (COL4), whose role in flowering control was unknown. We demonstrate that, unlike CO, COL4 is a flowering repressor in long days (LD) and short days (SD) and acts on the expression of FT and FT-like genes as well as on SUPPRESSOR OF OVEREXPRESSION OF CONSTANS 1 (SOC1). Reduction of COL4 expression level leads to an increase of FT and APETALA 1 (AP1) expression and to accelerated flowering, while the increase of COL4 expression causes a flowering delay. Further, the observed co-localization of COL4 protein and CO in nuclear speckles supports the idea that the two act as an antagonistic pair of transcription factors. This interaction may serve the fine-tuning of flowering time control and other light dependent plant developmental processes.

Highlights

  • Flowering is controlled by a network of well-established molecular pathways, which respond to internal and external signals, such as cold, light duration and quality, ambient temperature, as well as biotic and abiotic stresses

  • This effect was stronger in short days (SD) (Figure 1D), where both alleles flowered around 14 days earlier compared to wild-type (118 ± 3.4 days to bolting (DTB))

  • For plants the exact regulation of flowering time is critical for their reproductive success, whereby CO acts as a key activator of flowering in Arabidopsis and other plant species

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Summary

Introduction

Flowering is controlled by a network of well-established molecular pathways, which respond to internal and external signals, such as cold, light duration and quality, ambient temperature, as well as biotic and abiotic stresses (reviewed in: Andres and Coupland, 2012; Matsoukas et al, 2012; Leijten et al, 2018). In Arabidopsis, flowering is promoted mainly by the expression of the flowering integrators FLOWERING LOCUS T (FT), SUPPRESSOR OF CONSTANS 1 (SOC1/ AGL20) and, redundantly to FT, it’s homolog TWIN SISTER OF FT (TSF) (Suarez-Lopez et al, 2001; An et al, 2004; Valverde et al, 2004; Yamaguchi et al, 2005). In the SAM, the formation of an FD-14-3-3 complex with FT or ATC and the other FT-homolog TERMINAL FLOWER 1 (TFL), induces or delays flowering, respectively, by changing the expression of the meristem identity genes APETALA1 (AP1) and CAULIFLOWER (CAL) as well as LEAFY (LFY) and AGAMOUS-LIKE 24 (AGL24) (Abe et al, 2005; Liu et al, 2008; Hanano and Goto, 2011; Taoka et al, 2011). Reduction in CO level leads to late flowering in LD while overexpression promotes flowering in LD and SD (Putterill et al, 1995; Onouchi et al, 2000; Robson et al, 2001; Takada and Goto, 2003; Jang et al, 2008)

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