Abstract

Light is an important environmental cue that affects physiology and development of Neurospora crassa. The light-sensing transcription factor (TF) WCC, which consists of the GATA-family TFs WC1 and WC2, is required for light-dependent transcription. SUB1, another GATA-family TF, is not a photoreceptor but has also been implicated in light-inducible gene expression. To assess regulation and organization of the network of light-inducible genes, we analyzed the roles of WCC and SUB1 in light-induced transcription and nucleosome remodeling. We show that SUB1 co-regulates a fraction of light-inducible genes together with the WCC. WCC induces nucleosome eviction at its binding sites. Chromatin remodeling is facilitated by SUB1 but SUB1 cannot activate light-inducible genes in the absence of WCC. We identified FF7, a TF with a putative O-acetyl transferase domain, as an interaction partner of SUB1 and show their cooperation in regulation of a fraction of light-inducible and a much larger number of non light-inducible genes. Our data suggest that WCC acts as a general switch for light-induced chromatin remodeling and gene expression. SUB1 and FF7 synergistically determine the extent of light-induction of target genes in common with WCC but have in addition a role in transcription regulation beyond light-induced gene expression.

Highlights

  • Organisms synchronize their behavior and physiology with the geophysical day-night cycle by acute signal transduction of rhythmically reoccurring cues and via anticipatory processes controlled by circadian clocks

  • In this study we have investigated the roles of the Neurospora transcription factors (TFs) White Collar Complex (WCC) and SUB1 in light-activation of transcription

  • We found that the activity of the main blue-light photoreceptor WCC is essential for the activation of light-inducible genes

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Summary

Introduction

Organisms synchronize their behavior and physiology with the geophysical day-night cycle by acute signal transduction of rhythmically reoccurring cues and via anticipatory processes controlled by circadian clocks. Light-activation of WCC results in dynamic homo-dimerization of WCC protomers, which bind to specific light-responsive DNA elements (LREs) to activate transcription of target genes [15,19,20,21,22]. WCC is the core TF of the circadian clock of Neurospora It supports self-sustained circadian gene expression rhythms in the dark and synchronizes the circadian oscillator with rhythmic exogenous light cues [2,23,24,25,26]. The dark form of WCC supports a low amplitude circadian nucleosome occupancy rhythm at the socalled clock-box in the frq promoter [27,28] while light-activated WCC supports nucleosome remodeling at the light-responsive element (LRE) close to the transcriptional start site [29]. Substantial levels of sub are already expressed in the dark [19,30,31] and SUB1 target genes are still light-inducible to a lower extent in the absence of SUB1 [30] suggesting a more complex regulation of SUB1-dependent light-inducible genes

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