Gearing Up the Clock of Hypocotyl Growth!
To anticipate daily changes imposed by Earth’s rotation, organisms from all domains of life have evolved an endogenous 24-h timer with daily rhythmic functions: the circadian clock. In plants, the first organisms where circadian dynamics were observed, the circadian clock processes daylength information to regulate a wide range of physiological and developmental responses (Greenham and McClung, 2015). Under normal photoperiodic conditions, hypocotyl elongation is a robust response that can be observed to monitor the circadian regulation of plant growth (Nusinow et al., 2011). However, the regulatory networks controlling this physiological mechanism remains poorly understood.
In this issue of Plant Physiology, Li et al. (2020) approach this topic by demonstrating coordinated action of specific components of the Arabidopsis thaliana circadian clock to regulate photoperiodic hypocotyl growth (Li et al., 2020). They focused on the Evening Complex (EC), which is composed of EARLY FLOWERING 4 (ELF4), EARLY FLOWERING 3 (ELF3), and LUX ARRHYTHMO (LUX); and the Pseudo Response Regulators (PRRs) gene family composed of five members (PRR3, PRR5, PRR7, PRR9, and TIMING OF CAB EXPRESSION 1 (TOC1)), all components of the circadian clock. One of the functions of the EC and PRRs in plant photoperiodic growth dynamics is to regulate the abundance and activity of PHYTOCHROME-INTERACTING FACTOR (PIF) transcription factors, which are positive regulators of plant cell elongation (Nusinow et al., 2011; Martin et al., 2018). Previous work has demonstrated that, whereas EC components (ELF3, ELF4 and LUX) inhibit PIF expression in the early evening and the beginning of the night (thus directly allowing the circadian clock to diurnally regulate hypocotyl growth), PRR proteins (PRR3, PRR5, PRR7, PRR9 and TOC1) are proposed to modulate photoperiodic hypocotyl elongation via transcriptional regulation and post-transcriptional control of PIF4 and PIF5 (Liu et al., 2013; Martin et al., 2018). Since PIF proteins promote cell elongation, any conditions that promote PIF expression and accumulation, such as short days (SD) and high temperature, induce long hypocotyl phenotypes.
Li et al. (2020) used a series of higher order mutants to evaluate the genetic interactions of PRRs and EC components on hypocotyl length upon different light regimes (SD; LD, long day and LL, continuous light). They found that the hypocotyls of toc1 prr5 elf3 and toc1 prr5 lux triple mutants were significantly longer than those of lower order mutants, both in SD and LD, suggesting that PRR and EC additively regulate this growth response under photoperiodic conditions. Remarkably, LL conditions abolished any hypocotyl growth difference indicating that daylight cycling is required to reveal the role of clock genes on hypocotyl growth.
How do the EC and PRRs additively control PIF and what is the impact on the hypocotyl elongation? To address this, the authors carried out a transcriptomic study of various PRR mutants, which revealed that PRRs regulate PIF expression, as PIFs have been previously shown to be transcriptional targets of the EC. Previous studies have indicated that TOC1 protein also interacts with PIFs through direct protein-protein interactions. Here, the authors demonstrated that although the protein-protein interaction occurs independently of TOC1’s DNA binding domain, TOC1 requires its DNA binding domain to rescue a toc1 knockout mutant. These data support an important transcriptional role for TOC1 in regulating PIF expression levels and hypocotyl growth. The authors also showed that TOC1/PRR5 are able to directly bind PIF promoter regions and repress them.
More important, the authors showed that the circadian expression of PIF4 and PIF5 is cooperatively orchestrated by PRRs and EC acting at slightly different times of the evening, with PRRs repressing PIFs expression earlier than EC components. Using the toc1 prr5 elf3 triple mutant, the authors showed that daylength imposes dynamic changes on the expression of PIF4 and PIF5, depending on the presence of specific PRRs and EC. In doing so, PRRs and EC proteins adjust daylength information by affecting the cyclic expression of PIFs. Additionally, the toc1prr5 pif4 pif5 quadruple mutant showed that PRR-mediated clock regulation of hypocotyl elongation requires a functional PIF4 and PIF5 and hence PIF4 and PIF5 act downstream of PRRs. In other words, the coordination of the hypocotyl-growth response mediated by PIF4 and PIF5 is synchronized with daylength by the clock elements PRRs and EC.
Molecular characterization of the plant circadian clock is helping us to understand how plants regulate a plethora of daily rhythmic physiological events. As interconnected mechanical gears that control the functioning of a true physical clock, authors demonstrated that EC and PRR work additively to regulate circadian dynamics of photoperiodic hypocotyl growth. Given that hypocotyl growth is critical for the success of seedling establishment, work by Li et al. (2020) may allow us to understand the physiological processes controlling seedling establishment and plant survival in natural conditions. In this regard, synchrony between the external light-dark cycle and the internal plant clock results in improved growth and survival parameters (Green et al., 2002; Dodd et al., 2005). Besides photoperiodic growth, the described mechanism of work for the PRRs-EC-PIF signaling module may serve as a tool to explore other clock-modulated responses in plants, such as metabolites accumulation (Dodd et al., 2015), foraging for light (Salter et al., 2003) and defense against pests and pathogens (Goodspeed et al., 2013). The clock keeps ticking and the time to move circadian research into the wild is gearing up!
Javier Edgardo Moreno
javier.moreno@santafe-conicet.gov.ar
ORCID ID: 0000-0001-9763-5325
Twitter: @JaviMorenoOK
Instituto de Agrobiotecnología del Litoral (UNL-Conicet), Facultad de Bioquímica y Ciencias Biológicas, Universidad Nacional del Litoral
Santa Fe 3000, Argentina
Marcelo Lattarulo Campos
marcelo.lattarulo@gmail.com
ORCID ID: 0000-0001-6235-5120
Twitter: @lattarulo
Integrative Plant Research Laboratory, Departamento de Botânica e Ecologia, Instituto de Biociências, Universidade Federal de Mato Grosso
Cuiabá/MT, Brazil.
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