Glutamine synthetase activity and the expression of three glul paralogues in zebrafish during transport
- Authors
- Dhanasiri, A.K., Fernandes, J.M., and Kiron, V.
- ID
- ZDB-PUB-120706-10
- Date
- 2012
- Source
- Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology 163(3-4): 274-284 (Journal)
- Registered Authors
- Fernandes, Jorge
- Keywords
- glutamine synthetase, ammonia, transport, Glu/paralogues, splice variants, zebrafish
- MeSH Terms
-
- Ammonia/analysis
- Ammonia/metabolism
- Animals
- Base Sequence
- Computational Biology
- Equidae/classification
- Equidae/metabolism
- Equidae/physiology*
- Gene Expression Regulation, Enzymologic*
- Glucocorticoids/metabolism
- Glutamate-Ammonia Ligase/genetics*
- Glutamate-Ammonia Ligase/metabolism*
- Movement*
- Phylogeny
- RNA, Messenger/genetics
- RNA, Messenger/metabolism
- Response Elements/genetics
- Sequence Homology, Nucleic Acid*
- Water/chemistry
- PubMed
- 22750401 Full text @ Comp. Biochem. Physiol. B Biochem. Mol. Biol.
The enzyme glutamine synthetase (GS; glutamate-ammonia ligase, EC 6.3.1.2) plays an important role in the nitrogen metabolism of fish. In this study the GS activity and the corresponding genes were examined to understand how they are regulated in zebrafish in response to hyperammonemic stress during a 72 h simulated transport. Whole body ammonia levels, the activity of the enzyme GS and the mRNA expression of the splice variants of three paralogues of glul, glutamine synthetase gene (glula, glulb and glulc) were examined in brain, liver and kidney of zebrafish. Whole body ammonia reached significantly higher levels by 48 h, while brain showed higher levels as early as 24 h, compared to the values at the start of the transport. The GS activities in brain, liver and kidney were significantly higher at the end of 72 h transport than those at the start. However, only the expression of mRNA of glulb-002 and glulb-003 were significantly upregulated during the simulated transport. In silico analysis of the putative promoter regions of glul paralogues revealed glucocorticoid receptor binding sites. However, glucocorticoid response elements of glulb were not different. The up-regulation of GS enzyme activity and hitherto unreported mRNA expression of glul paralogues during zebrafish transport indicate a physiological response of fish to ammonia.