Effects of crowding on ornithine–urea cycle enzyme mRNA expression and activity in gulf toadfish (Opsanus beta)

Author:

Laberge Tammy1,Walsh Patrick J.2,McDonald M. Danielle1

Affiliation:

1. Division of Marine Biology and Fisheries, Rosenstiel School of Marine and Atmospheric Science, University of Miami, 4600 Rickenbacker Causeway, Miami,FL 33149, USA

2. Department of Biology, Centre for Advanced Research in Environmental Genomics,University of Ottawa, 30 Marie Curie, Ottawa, ON, Canada K1N 6N5

Abstract

SUMMARY The gulf toadfish (Opsanus beta) is a facultatively ureotelic fish that excretes primarily urea under conditions of crowding or confinement. To examine the relationship between ammonia production, urea production and the ornithine–urea cycle (O–UC) enzyme activity and mRNA expression,we subjected toadfish to two-day and seven-day crowding regimes. Plasma cortisol levels were measured and liver tissue was assayed for ammonia and urea concentrations. Liver glutamine synthetase (GS), carbamoyl phosphate synthetase III (CPS), ornithine carbamoyl transferase (OCT) and arginase (ARG)activities were also measured. Quantitative PCR was utilized to determine liver GS, CPS, OCT, ARG, argininosuccinate synthetase (ASS) and argininosuccinate lyase (ASL) mRNA expression. Hepatic ammonia concentrations decreased with increased duration of crowding whereas liver urea and circulating cortisol levels increased. An elevation in enzyme activity with increased duration of crowding was observed for all four O-UC enzymes examined. By contrast, mRNA expression was variable for the O–UC enzymes and only CPS and ASS had mRNA expression levels that were elevated in crowded fish. These results suggest that the activities of O–UC enzymes are better predictors for urea production than O–UC enzyme mRNA expression levels.

Publisher

The Company of Biologists

Subject

Insect Science,Molecular Biology,Animal Science and Zoology,Aquatic Science,Physiology,Ecology, Evolution, Behavior and Systematics

Reference43 articles.

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2. Anderson, P. M. (1995). Urea cycle in fish:molecular and mitochondrial studies. In Ionoregulation: Cellular and Molecular Approaches, vol. 14 (ed. C. M. Wood and T. J. Shuttleworth), pp. 57-83. New York:Academic Press.

3. Anderson, P. M. (2001). Urea and glutamine synthesis: environmental influences of nitrogen excretion. In Nitrogen Excretion (ed. P. A. Wright and P. M. Anderson), pp. 239-277. San Diego, CA: Academic Press.

4. Barber, M. L. and Walsh, P. J. (1993). Interactions of acid–base status and nitrogen excretion and metabolism in the ureogenic teleost Opsanus beta. J. Exp. Biol.185,87-105.

5. Brockmann, R., Beyer, A., Heinisch, J. J. and Wilhelm, T.(2007). Posttranscriptional expression regulation: what determines translation rates? PLoS Comput. Biol.3,0531-0539.

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