Expression patterns of zebrafish nocturnin genes and the transcriptional activity of the frog nocturnin promoter in zebrafish rod photoreceptors.
- Yang, X., Fu, J., Wei, X.
- Molecular Vision 23: 1039-1047 (Journal)
- Registered Authors
- Wei, Xiangyun
- MeSH Terms
- Amino Acid Sequence
- Animals, Genetically Modified
- Circadian Rhythm/physiology
- Gene Amplification
- Gene Expression Regulation/physiology*
- Gene Transfer Techniques
- Green Fluorescent Proteins/genetics
- Green Fluorescent Proteins/metabolism
- In Situ Hybridization
- Microscopy, Confocal
- Molecular Sequence Data
- Nuclear Proteins/genetics*
- Promoter Regions, Genetic/genetics*
- RNA, Messenger/genetics
- Real-Time Polymerase Chain Reaction
- Retinal Rod Photoreceptor Cells/metabolism*
- Reverse Transcriptase Polymerase Chain Reaction
- Sequence Homology
- Transcription Factors/genetics*
- Transcriptional Activation/physiology*
- Xenopus Proteins/genetics*
- Xenopus laevis
- Zebrafish Proteins/genetics*
Yang, X., Fu, J., Wei, X. (2017) Expression patterns of zebrafish nocturnin genes and the transcriptional activity of the frog nocturnin promoter in zebrafish rod photoreceptors.. Molecular Vision. 23:1039-1047.
Purpose Daily modulation of gene expression is critical for the circadian rhythms of many organisms. One of the modulating mechanisms is based on nocturnin, a deadenylase that degrades mRNA in a circadian fashion. The nocturnin genes are expressed broadly, but their tissue expression patterns differ between mice and the frog Xenopus laevis; this difference suggests that the extent of the regulation of nocturin gene expression varies among species. In this study, we set out to characterize the expression patterns of two zebrafish nocturnin genes; in addition, we asked whether a frog nocturnin promoter has transcriptional activity in zebrafish.
Methods We used reverse transcription (RT)-PCR, quantitative real-time PCR (qRT-PCR), and rapid amplification of cDNA ends (RACE) analysis to determine whether the nocturnin-a and nocturnin-b genes are expressed in the eye, in situ hybridization to determine the cellular expression pattern of the nocturnin-b gene in the retina, and confocal microscopy to determine the protein expression pattern of the transgenic reporter green fluorescent protein (GFP) driven by the frog nocturnin promoter.
Results We found that the amino acid sequences of zebrafish nocturnin-a and nocturnin-b are highly similar to those of frog, mouse, and human nocturnin homologs. Only nocturnin-b is expressed in the eye. Within the retina, nocturnin-b mRNA was expressed at higher levels in the retinal photoreceptors layer than in other cellular layers. This expression pattern echoes the restricted photoreceptor expression of nocturnin in the frog. We also found that the frog nocturnin promoter can be specifically activated in zebrafish rod photoreceptors.
Conclusions The high level of similarities in amino acid sequences of human, mouse, frog, and zebrafish nocturnin homologs suggest these proteins maintain a conserved deadenylation function that is important for regulating retinal circadian rhythmicity. The rod-specific transcriptional activity of the frog nocturnin promoter makes it a useful tool to drive moderate and rod-specific transgenic expression in zebrafish. The results of this study lay the groundwork to study nocturnin-based circadian biology of the zebrafish retina.
Genes / Markers
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Engineered Foreign Genes