Ontogeny of ornithine-urea cycle gene expression in zebrafish (Danio rerio)
- Authors
- Lemoine, C.M., and Walsh, P.J.
- ID
- ZDB-PUB-130418-19
- Date
- 2013
- Source
- American journal of physiology. Regulatory, integrative and comparative physiology 304(11): R991-R1000 (Journal)
- Registered Authors
- Keywords
- ureogenesis, nitrogen metabolism, development, ammonia challenge
- MeSH Terms
-
- Aging/genetics*
- Aging/metabolism*
- Ammonia/metabolism
- Animals
- Base Sequence
- Carbon-Nitrogen Ligases/genetics
- Carbon-Nitrogen Ligases/metabolism
- Digoxigenin
- Embryo, Nonmammalian
- Gene Expression/genetics*
- Gene Silencing
- In Situ Hybridization, Fluorescence
- Molecular Sequence Data
- Ornithine/genetics*
- Ornithine/metabolism*
- RNA Probes
- Real-Time Polymerase Chain Reaction
- Urea/metabolism*
- Zebrafish/genetics*
- Zebrafish/metabolism*
- PubMed
- 23576614 Full text @ Am. J. Physiol. Regul. Integr. Comp. Physiol.
Although the majority of adult teleosts excrete most of their nitrogenous wastes as ammonia, several fish species are capable of producing urea early in their development. In zebrafish, it is unclear if this results from a functional ornithine-urea cycle (O-UC) and, if so, how it might be regulated. This study examined the spatiotemporal patterns of gene expression of four major O-UC enzymes, carbamoyl phosphate synthase III (CPSIII), ornithine transcarboxylase, arginosuccinate synthetase and arginosuccinate lyase, using real-time PCR and whole mount in situ hybridization. In addition, we hypothesized that the gene expression of CPSIII was epigenetically regulated through methylation of its promoter. Further, to assess the functionality of CPSIII, we used morpholinos to silence CPSIII in zebrafish embryos and assessed their nitrogenous waste handling during development, and in response to an ammonia injection. Our results suggest that O-UC enzymes mRNAs are expressed early in zebrafish development, and colocalize to the embryonic endoderm. In addition, the methylation status of CPSIII promoter is not consistent with the patterns of expression observed in developing larvae or adult tissues, suggesting other means of transcriptional regulation of this key enzyme. Finally, CPSIII morphants exhibited a transient reduction in CPSIII enzyme activity at 24 hours post fertilization, which was paralleled by a reduction in urea production during development and in response to an ammonia challenge. Overall, we conclude that the O-UC is functional in zebrafish embryos, providing further evidence that the capacity to produce urea via the O-UC is widespread in developing teleosts.