Abstract

BackgroundIt has been previously reported that most mammalian genes display a circadian oscillation in their baseline expression. Consequently, the phase and amplitude of each component of a signal transduction cascade has downstream consequences.ResultsHere, we report our analysis of alternative transcripts in the leptin signaling pathway which is responsible for the systemic regulation of macronutrient storage and energy balance. We focused on the circadian expression pattern of a critical component of the leptin signaling system, suppressor of cytokine signaling 3 (SOCS3). On an Affymetrix GeneChip 430A2 microarray, this gene is represented by three probe sets targeting different regions within the 3' end of the last exon. We demonstrate that in murine brown adipose tissue two downstream 3' probe sets experience circadian baseline oscillation in counter-phase to the upstream probe set. Such differences in expression patterns are a telltale sign of alternative splicing within the last exon of SOCS3. In contrast, all three probe sets oscillated in a common phase in murine liver and white adipose tissue. This suggests that the regulation of SOCS3 expression in brown fat is tissue specific. Another component of the signaling pathway, Janus kinase (JAK), is directly regulated by SOCS and has alternative transcript probe sets oscillating in counter-phase in a white adipose tissue specific manner.ConclusionWe hypothesize that differential oscillation of alternative transcripts may provide a mechanism to maintain steady levels of expression in spite of circadian baseline variation.

Highlights

  • It has been previously reported that most mammalian genes display a circadian oscillation in their baseline expression

  • Leptin is highly expressed in adipose tissue and secreted into the bloodstream

  • suppressor of cytokine signaling 3 (SOCS3), whose transcription is activated by STAT3, represses both Janus kinase (JAK) and leptin receptor (LEPR) and serves to attenuate the signal

Read more

Summary

Introduction

It has been previously reported that most mammalian genes display a circadian oscillation in their baseline expression. Entrained by the daily light/dark cycle, feeding behavior, sleeping pattern and/or other environmental and physiological cues, gene expression patterns demonstrate daily oscillations. It has been widely accepted that up to 10–15 per cent of all genes are expressed following a circadian rhythm [1], generated by (page number not for citation purposes). The central circadian clock is synchronized to the daily light/dark cycle and is located in the Suprachiasmic Nucleus (SCN) of the hypothalamus. Since virtually every component of each biological pathway is oscillating, the timing of regulation, interaction or signal transduction is critically important as well as the phase of oscillation at which a particular event takes place

Methods
Results
Discussion
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call