PUBLICATION

Microcystin-induced variations in transcription of GSTs in an omnivorous freshwater fish, goldfish

Authors
Li, G., Xie, P., Fu, J., Hao, L., Xiong, Q., and Li, H.
ID
ZDB-PUB-080506-10
Date
2008
Source
Aquatic toxicology (Amsterdam, Netherlands)   88(1): 75-80 (Journal)
Registered Authors
Keywords
Microcystin, Glutathione S-transferases, Real-time PCR, Goldfish, Carassius auratus L
MeSH Terms
  • Animals
  • Cloning, Molecular
  • Fresh Water
  • Gene Expression Regulation, Enzymologic/drug effects*
  • Glutathione Transferase/genetics*
  • Glutathione Transferase/metabolism
  • Goldfish/genetics*
  • Microcystins/pharmacology*
  • Molecular Sequence Data
  • Phylogeny
  • Protein Isoforms/genetics
  • Time Factors
  • Transcription, Genetic/drug effects*
PubMed
18455246 Full text @ Aquat. Toxicol.
Abstract
The glutathione S-transferases are important enzymes in the microcystin-induced detoxication processes. In this experiment, we cloned the full-length cDNA of alpha, pi and theta-class-like glutathione S-transferase genes from goldfish (Carassius auratus L). Their derived amino acid sequences were clustered with other vertebrate alpha, pi and theta-class GSTs in a phylogenetic tree and the goldfish GST sequences have the highest similarity with those from common carp and zebrafish. Goldfish were i.p. injected with microcystins extract at two doses (50 and 200mugkg(-1)BW MC-LR(eq)) and the relative changes of the mRNA abundance in liver, kidney and intestine were analyzed by real-time PCR. The transcription of GST alpha was suppressed in both liver and intestine, but induced in the kidney. Decreased transcription of GST theta was detected in liver, kidney and intestine in the low-dose group. The transcription of GST pi was suppressed in liver and intestine post-injection in both dose groups. These results suggested that the transcription of GST isoforms varied in different ways within an organ and among organs of goldfish exposed to MCs.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping