Abstract

Background24-hour biological clocks are intimately connected to the cellular signalling network, which complicates the analysis of clock mechanisms. The transcriptional regulator TOC1 (TIMING OF CAB EXPRESSION 1) is a founding component of the gene circuit in the plant circadian clock. Recent results show that TOC1 suppresses transcription of multiple target genes within the clock circuit, far beyond its previously-described regulation of the morning transcription factors LHY (LATE ELONGATED HYPOCOTYL) and CCA1 (CIRCADIAN CLOCK ASSOCIATED 1). It is unclear how this pervasive effect of TOC1 affects the dynamics of the clock and its outputs. TOC1 also appears to function in a nested feedback loop that includes signalling by the plant hormone Abscisic Acid (ABA), which is upregulated by abiotic stresses, such as drought. ABA treatments both alter TOC1 levels and affect the clock’s timing behaviour. Conversely, the clock rhythmically modulates physiological processes induced by ABA, such as the closing of stomata in the leaf epidermis. In order to understand the dynamics of the clock and its outputs under changing environmental conditions, the reciprocal interactions between the clock and other signalling pathways must be integrated.ResultsWe extended the mathematical model of the plant clock gene circuit by incorporating the repression of multiple clock genes by TOC1, observed experimentally. The revised model more accurately matches the data on the clock’s molecular profiles and timing behaviour, explaining the clock’s responses in TOC1 over-expression and toc1 mutant plants. A simplified representation of ABA signalling allowed us to investigate the interactions of ABA and circadian pathways. Increased ABA levels lengthen the free-running period of the clock, consistent with the experimental data. Adding stomatal closure to the model, as a key ABA- and clock-regulated downstream process allowed to describe TOC1 effects on the rhythmic gating of stomatal closure.ConclusionsThe integrated model of the circadian clock circuit and ABA-regulated environmental sensing allowed us to explain multiple experimental observations on the timing and stomatal responses to genetic and environmental perturbations. These results crystallise a new role of TOC1 as an environmental sensor, which both affects the pace of the central oscillator and modulates the kinetics of downstream processes.

Highlights

  • Circadian clocks allow most eukaryotes and some prokaryotes to anticipate the environmental day/night cycle, through rhythmic modulation of multiple physiological processes [1]

  • We have included a simplified version of the main steps leading to the induction of TIMING OF CAB EXPRESSION 1 (TOC1) by Abscisic Acid (ABA) and the regulation of stomata aperture (Figure 1B), described in the section 2 below

  • evening complex (EC) (EVENING COMPLEX) genes LUX ARRHYTHMO (LUX), ELF3 (EARLY FLOWERING 3) and EARLY FLOWERING 4 (ELF4) are expressed around dusk and form the EC protein complex, which suppresses expression of multiple

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Summary

Introduction

Circadian clocks allow most eukaryotes and some prokaryotes to anticipate the environmental day/night cycle, through rhythmic modulation of multiple physiological processes [1]. Circadian clocks are characterised by free running rhythms with a period of ~24 h even in the absence of any environmental cues, such as in constant light conditions. Their timing is synchronised with the environmental day-night cycle principally by responses to light and temperature, but clock circuits respond to many additional stimuli. The signalling pathways from such stimuli are often found to be rhythmically controlled by the clock, forming nested feedback loops that modify the circadian oscillator. TOC1 is an important component of the plant clock since its mutation or overexpression dramatically change the properties of the central oscillator [3]

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