PUBLICATION

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
  • Animals
  • Digoxigenin
  • Urea/metabolism*
  • Gene Silencing
  • Zebrafish/genetics*
  • Zebrafish/metabolism*
  • Base Sequence
  • Molecular Sequence Data
  • Aging/genetics*
  • Aging/metabolism*
  • Ornithine/genetics*
  • Ornithine/metabolism*
  • Real-Time Polymerase Chain Reaction
  • In Situ Hybridization, Fluorescence
  • Ammonia/metabolism
  • RNA Probes
  • Carbon-Nitrogen Ligases/genetics
  • Carbon-Nitrogen Ligases/metabolism
  • Embryo, Nonmammalian
  • Gene Expression/genetics*
(all 20)
PubMed
23576614 Full text @ Am. J. Physiol. Regul. Integr. Comp. Physiol.
Abstract

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.

Genes / Markers
Figures
No images available
Show all Figures
Expression
Phenotype
1 - 1 of 1
Show
Mutations / Transgenics
No data available
Human Disease / Model
No data available
Sequence Targeting Reagents
Target Reagent Reagent Type
cps1MO1-cps1MRPHLNO
1 - 1 of 1
Show
Fish
1 - 2 of 2
Show
Antibodies
Orthology
Engineered Foreign Genes
No data available
Mapping