PUBLICATION

Analysis of a gene regulatory cascade mediating circadian rhythm in zebrafish

Authors
Li, Y., Li, G., Wang, H., Du, J., and Yan, J.
ID
ZDB-PUB-130402-4
Date
2013
Source
PLoS Computational Biology   9(2): e1002940 (Journal)
Registered Authors
Du, Jiu Lin
Keywords
none
Datasets
GEO:GSE37332
MeSH Terms
  • Animals
  • Circadian Rhythm/genetics
  • Circadian Rhythm/physiology*
  • Circadian Rhythm Signaling Peptides and Proteins/genetics
  • Circadian Rhythm Signaling Peptides and Proteins/metabolism
  • Circadian Rhythm Signaling Peptides and Proteins/physiology*
  • Databases, Protein
  • Gene Regulatory Networks/genetics
  • Gene Regulatory Networks/physiology*
  • Larva
  • Light
  • Melanins/chemistry
  • Melanins/metabolism
  • Mice
  • Transcription Factors
  • Zebrafish
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism
  • Zebrafish Proteins/physiology*
PubMed
23468616 Full text @ PLoS Comput. Biol.
Abstract

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.

Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping