ZFIN ID: ZDB-PUB-080616-10
Detection of Mercury in Aquatic Environments Using EPRE Reporter Zebrafish
Kusik, B.W., Carvan Iii, M.J., and Udvadia, A.J.
Date: 2008
Source: Marine biotechnology (New York, N.Y.)   10(6): 750-757 (Journal)
Registered Authors: Kusik, Brandon, Udvadia, Ava J.
Keywords: Transgenic zebrafish, Oxidative stress, Electrophile response element, Antioxidant response element, EPRE, ARE
MeSH Terms:
  • Animals
  • Animals, Genetically Modified/genetics
  • Animals, Genetically Modified/metabolism
  • Embryo, Nonmammalian/drug effects
  • Embryo, Nonmammalian/metabolism
  • Environmental Monitoring*
  • Gene Expression
  • Gene Expression Regulation, Developmental
  • Genes, Reporter*
  • Green Fluorescent Proteins/genetics
  • Green Fluorescent Proteins/metabolism
  • Luciferases/genetics
  • Luciferases/metabolism
  • Mercuric Chloride/toxicity*
  • Oxidative Stress
  • Response Elements
  • Transgenes
  • Water Pollutants, Chemical/metabolism*
  • Zebrafish/genetics*
  • Zebrafish/metabolism
PubMed: 18537037 Full text @ Mar. Biotechnol.
ABSTRACT
It has been proposed that transgenic zebrafish could be designed to detect low levels of chemical contaminants that cause oxidative stress in aquatic environments, such as heavy metals or pesticides. In this paper, we describe such a transgenic zebrafish that produces a luciferase-green fluorescent protein (LUC-GFP) fusion protein under conditions of oxidative stress. The reporter gene expression is under the regulation of the electrophile responsive element (EPRE), which activates gene expression in response to oxidative stressors. The GFP component of this fusion protein allows us to visually detect reporter gene activity in live animals to determine if activity is localized to a particular tissue. The luciferase component is capable of returning a quantitative assessment of reporter gene activity that allows us to determine if reporter gene activity is directly correlated to the concentration of the chemical inducer. We have tested this reporter construct in both transient and stable transgenic fish after exposure to a range of HgCl(2) concentrations. GFP expression from the EPRE-LUC-GFP construct was inducible in transient assays but was below the limit of detection in stable lines. In contrast, we observed inducible luciferase activity in both transient assays and stable lines treated with HgCl(2). We conclude that the EPRE is capable of driving reporter gene expression in a whole animal assay under conditions of oxidative stress. Furthermore, expression was induced at HgCl(2) concentrations that do not result in obvious morphological defects, making this approach useful for the detection of low levels of oxidative contaminants in aquatic environments.
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