Genome-wide identification and expression of the entire 52 glutathione S-transferase (GST) subfamily genes in the Cu2+-exposed marine copepods Tigriopus japonicus and Paracyclopina nana

Aquat Toxicol. 2019 Apr:209:56-69. doi: 10.1016/j.aquatox.2019.01.020. Epub 2019 Jan 24.

Abstract

In this study, the entire glutathione S-transferases (GSTs), the major phase II detoxification enzyme, were identified in two marine copepod species Tigriopus japonicus and Paracyclopina nana. The genome-wide identification of GSTs in T. japonicus and P. nana resulted in 32 and 20 GSTs in total, respectively. Among the identified GSTs, two specific classes of GSTs, specifically sigma and delta/epsilon GSTs were the dominant form of cytosolic GSTs in T. japonicus, while delta/epsilon and mu classes were dominant cytosolic GSTs in P. nana. In addition, Membrane-Associated Proteins in Eicosanoid and Glutathione metabolism (MAPEG) family were found in relatively higher proportion compared to other classes. Moreover, sigma, delta/epsilon, and microsomal GSTs have shown to expand through tandem duplication. To validate the detoxification function of the identified GSTs, both copepods were exposed to copper (Cu2+) and the reactive oxygen species (ROS) level and GST activity were measured. With integration of phylogenetic analysis and xenobiotic-mediated GST mRNA expression patterns along with previous enzymatic activities, the functional divergence among species-specific GST genes was clearly observed. This study covers full identification of GST classes in two marine copepod species and their important role in marine environmental ecotoxicology.

Keywords: Copepod; Detoxification; Genome-wide identification; Glutathione S-transferase; Tandem duplication.

MeSH terms

  • Animals
  • Aquatic Organisms / drug effects
  • Aquatic Organisms / enzymology
  • Aquatic Organisms / genetics*
  • Copepoda / drug effects
  • Copepoda / enzymology*
  • Copepoda / genetics*
  • Copper / toxicity*
  • Gene Duplication
  • Gene Expression Regulation, Enzymologic / drug effects*
  • Genome*
  • Glutathione Transferase / genetics*
  • Inactivation, Metabolic / drug effects
  • Multigene Family*
  • Phylogeny
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Reactive Oxygen Species / metabolism
  • Synteny / genetics
  • Time Factors
  • Toxicity Tests, Acute
  • Transcription, Genetic / drug effects
  • Water Pollutants, Chemical / toxicity

Substances

  • RNA, Messenger
  • Reactive Oxygen Species
  • Water Pollutants, Chemical
  • Copper
  • Glutathione Transferase