4.7 Article

Characterization of glutathione-S-transferases in zebrafish (Danio rerio)

Journal

AQUATIC TOXICOLOGY
Volume 158, Issue -, Pages 50-62

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.aquatox.2014.10.013

Keywords

Glutathione-S-transferases; Zebrafish; Phylogenetic analysis; mRNA expression; Enzyme kinetics; Functional characterization

Funding

  1. Ministry for Science, Technology and Sports of the Republic of Croatia [098-0982934-2745]
  2. Swiss National Science Foundation (SNSF) [SCOPES-IZ73Z0_128025/1]
  3. Serbian Ministry of Education, Science and Technological Development [173037]

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Glutathione-S-transferases (GSTs) are one of the key enzymes that mediate phase II of cellular detoxification. The aim of our study was a comprehensive characterization of GSTs in zebrafish (Dania rerio) as an important vertebrate model species frequently used in environmental research. A detailed phylagenetic analysis of GST superfamily revealed 27 zebrafish gst genes. Further insights into the orthology relationships between human and zebrafish GSTs/Gsts were obtained by the conserved synteny analysis. Expression of gst genes in six tissues (liver, kidney, gills, intestine, brain and gonads) of adult male and female zebrafish was determined using qRT-PCR. Functional characterization was performed on 9 cytosolic Gst enzymes after overexpression in E. coli and subsequent protein purification. Enzyme kinetics was measured for GSH and a series of model substrates. Our data revealed ubiquitously high expression of gstp, gstm (except in liver), gstr1, mgst3a and mgst3b, high expression of gsto2 in gills and ovaries, gsta in intestine and testes, gstt1 a in liver, and gstz1 in liver, kidney and brain. All zebrafish Gsts catalyzed the conjugation of GSH to model GST substrates 1-chloro-2,4-dinitrobenzene (CDNB) and monochlorobimane (MCB), apart from Gsto2 and Gstz1 that catalyzed GSH conjugation to dehydroascorbate (DHA) and dichloroacetic acid (DCA), respectively. Affinity toward CDNB varied from 0.28 mM (Gstp2) to 3.69 mM (Gstm3), while affinity toward MCB was in the range of 5 mu M (Gstt1a) to 250 mu M (Gstp1). Affinity toward GSH varied from 0.27 mM (Gstz1) to 4.45 mM (Gstt1a). Turnover number for CDNB varied from 5.25 s(-1) (Gstt1a) to 112 s(-1) (Gstp2). Only Gst Pi enzymes utilized ethacrynic acid (ETA). We suggest that Gstp1, Gstp2, Gstt1a, Gstz1, Gstr1, Mgst3a and Mgst3b have important role in the biotransformation of xenobiotics, while Gst Alpha, Mu, Pi, Zeta and Rho classes are involved in the crucial physiological processes. In summary, this study provides the first comprehensive analysis of GST superfamily in zebrafish, presents new insight into distinct functions of individual Gsts, and offers methodological protocols that can be used for further verification of interaction of environmental contaminants with fish Gsts. (C) 2014 Elsevier B.V. All rights reserved.

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