Molecular cloning of cDNA encoding a ubiquitin-activating enzyme (E1) from goldfish (Carassius auratus) and expression analysis of the cloned gene

Biochim Biophys Acta. 2000 Jun 21;1492(1):259-63. doi: 10.1016/s0167-4781(00)00091-9.

Abstract

Destruction of cyclin B is required to the mitotic and meiotic cycles. A cyclin-specific ubiquitinating system, including ubiquitin-activating enzyme (E1), is thought to be responsible for cyclin B destruction. Here we present the cloning, sequencing and expression analysis of goldfish, Carassius auratus, E1 from goldfish ovary. The cloned cDNA is 4069 bp long and encodes 1059 amino acids. The deduced amino acid sequence is highly homologous to E1 from other species. Recombinant goldfish E1 could transfer ubiquitin to cyclin-selective ubiquitin-conjugating enzyme. Tissue distribution revealed a single 4.0-kb message ubiquitous among tissues.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Blotting, Northern
  • Cloning, Molecular
  • DNA, Complementary / analysis
  • Gene Expression
  • Goldfish / genetics*
  • Humans
  • Ligases / genetics*
  • Molecular Sequence Data
  • Sequence Homology, Amino Acid
  • Tissue Distribution
  • Ubiquitin-Activating Enzymes
  • Ubiquitin-Protein Ligases

Substances

  • DNA, Complementary
  • Ubiquitin-Protein Ligases
  • Ligases
  • Ubiquitin-Activating Enzymes