PUBLICATION
Dual NRF2 paralogs in Coho salmon and their antioxidant response element targets
- Authors
- Ramsden, R., Gallagher, E.P.
- ID
- ZDB-PUB-160730-9
- Date
- 2016
- Source
- Redox Biology 9: 114-123 (Journal)
- Registered Authors
- Gallagher, Evan P.
- Keywords
- Antioxidant response element, Coho salmon, Nrf2, Nuclear factor erythroid 2-like 2, Paralog
- MeSH Terms
-
- Amino Acid Sequence
- Animals
- Antioxidant Response Elements*
- Cell Line
- Gene Expression Regulation*
- NF-E2-Related Factor 2/chemistry
- NF-E2-Related Factor 2/genetics*
- NF-E2-Related Factor 2/metabolism
- Oxidation-Reduction
- Oxidative Stress
- Phylogeny
- Protein Isoforms
- Protein Multimerization
- Salmon/classification
- Salmon/genetics*
- Salmon/metabolism
- Zebrafish
- PubMed
- 27470083 Full text @ Redox Biol.
Citation
Ramsden, R., Gallagher, E.P. (2016) Dual NRF2 paralogs in Coho salmon and their antioxidant response element targets. Redox Biology. 9:114-123.
Abstract
The transcription factor NFE2L2 (Nuclear Factor, Erythroid 2-Like 2, or NRF2) plays a key role in maintaining the redox state within cells. Characterization of this pathway has extended to fish, most notably zebrafish (Danio rerio), in which two paralogs of the transcription factor exist: Nrf2a, an activator, and Nrf2b, a negative regulator during embryogenesis. Only one ARE target has been thoroughly delineated in zebrafish, and this deviated from the canonical sequence derived from studies in mammals. In general, the mechanistic pathway has not been characterized in non-model aquatic organisms that are commonly exposed to environmental pollutants. The current study compares the zebrafish paralogs to those found in a non-model teleost, the ecologically important salmonid, Oncorhnychus kisutch (coho salmon). Two salmon paralogs, Nrf2A and -2B, described here were found to possess only slightly greater identity between one another (84% of amino acids) than to the singleton ortholog of the esocid Esox lucius (80-82%), the nearest non-salmonid outgroup. Unlike one of the zebrafish forms, each is a strong activating factor based on sequence homology and in vitro testing. To uncover functional target AREs in coho, promoter flanking sequences were isolated for five genes that protect cells against oxidative stress: heme oxygenase 1, peroxiredoxin 1, glutamate-cysteine ligase, and the glutathione S-transferases pi and rho (hmox1, prdx1, gclc, gstp, and gstr). All except gstr had functional elements and all fit the standard mammalian-derived canonical sequence, unlike the motif found in zebrafish gstp. Expression studies demonstrate the presence of both Nrf2 paralogs in multiple organs, although in differing ratios. Collectively, our findings extend the conservation of Nrf2 and the ARE to salmonids, and should help inform future work in teleosts on mechanisms of redox control, as well as responsiveness of this pathway and its downstream antioxidant gene targets to chemical exposures in the environment.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping