Abstract

In Drosophila, CLOCK/CYCLE heterodimer (CLK/CYC) is the primary activator of circadian clock genes that contain the E-box sequence in their promoter regions (hereafter referred to as “E-box clock genes”). Although extensive studies have investigated the feedback regulation of clock genes, little is known regarding other factors acting with CLK/CYC. Here we show that Drosophila C-terminal binding protein (dCtBP), a transcriptional co-factor, is involved in the regulation of the E-box clock genes. In vivo overexpression of dCtBP in clock cells lengthened or abolished circadian locomotor rhythm with up-regulation of a subset of the E-box clock genes, period (per), vrille (vri), and PAR domain protein 1ε (Pdp1ε). Co-expression of dCtBP with CLK in vitro also increased the promoter activity of per, vri, Pdp1ε and cwo depending on the amount of dCtBP expression, whereas no effect was observed without CLK. The activation of these clock genes in vitro was not observed when we used mutated dCtBP which carries amino acid substitutions in NAD+ domain. These results suggest that dCtBP generally acts as a putative co-activator of CLK/CYC through the E-box sequence.

Highlights

  • Many organisms show circadian rhythms in physiology, metabolism, and behavior

  • We revealed that Drosophila C-terminal binding protein (dCtBP) acts as a putative coactivator of CLOCK/CYCLE heterodimer (CLK/CYC) in the transcription of a subset of the Ebox clock genes both in vivo and in vitro and its NAD+ domain is essential for the activation

  • We found EP3352 strain carrying the Upstream Activation Sequence (UAS) insertion in the promoter region of dCtBP altered circadian locomotor rhythm when it was crossed with tim(UAS)-Gal4

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Summary

Introduction

Many organisms show circadian rhythms in physiology, metabolism, and behavior. These rhythms are controlled by an endogenous circadian clock [1]. PER/TIM suppresses the function of CLK/CYC to generate the oscillation of their own transcription. In another loop, the transcription of Clk is mediated by VRI and PDP1e which acts as a suppressor and an activator, respectively. CWO inhibits the transcription of clock genes to bind the E-box sequence This interlocked feedback loops generate and maintain circadian rhythm in pacemaker cells in the Drosophila head and regulate circadian output pathways that control circadian rhythms in physiology, metabolism, and behavior. We revealed that dCtBP acts as a putative coactivator of CLK/CYC in the transcription of a subset of the Ebox clock genes both in vivo and in vitro and its NAD+ domain is essential for the activation

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