PLoS Computational Biology · 2013 · 76 citations · 58 references
Life SciencesBiologyMolecular BiologyCircadian RhythmsGene ExpressionTranscriptional RegulationCircadian Clock MechanismsCircadian Gene ExpressionCircadian Molecular MechanismsCircadian PhysiologyGene Regulation In PhysiologyTranscriptomics In FishCircadian ClocksCircadian Regulation Of Gene ExpressionCircadian Rhythm Gene ExpressionCircadian Transcriptional RegulationClock Gene Transcriptional RegulationLight-dark Cycle EntrainmentLight-dark Cycle ResponsesLight-entrained Gene Expression
In the study of circadian rhythms, it has been a puzzle how a limited number of circadian clock genes can control diverse aspects of physiology. Here we investigate circadian gene expression genome-wide using larval zebrafish as a model system. We made use of a spatial gene expression atlas to investigate the expression of circadian genes in various tissues and cell types. Comparison of genome-wide circadian gene expression data between zebrafish and mouse revealed a nearly anti-phase relationship and allowed us to detect novel evolutionarily conserved circadian genes in vertebrates. We identified three groups of zebrafish genes with distinct responses to light entrainment: fast light-induced genes, slow light-induced genes, and dark-induced genes. Our computational analysis of the circadian gene regulatory network revealed several transcription factors (TFs) involved in diverse aspects of circadian physiology through transcriptional cascade. Of these, microphthalmia-associated transcription factor a (mitfa), a dark-induced TF, mediates a circadian rhythm of melanin synthesis, which may be involved in zebrafish's adaptation to daily light cycling. Our study describes a systematic method to discover previously unidentified TFs involved in circadian physiology in complex organisms.
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