Molecular cloning of cDNA encoding a cyclin-selective ubiquitin carrier protein (E2-C) from Curassius auratus (goldfish) and expression analysis of the cloned gene
M. Tokumoto et al., Molecular cloning of cDNA encoding a cyclin-selective ubiquitin carrier protein (E2-C) from Curassius auratus (goldfish) and expression analysis of the cloned gene, FEBS LETTER, 458(3), 1999, pp. 375-377
Destruction of cyclin B is required for exit from mitosis and meiosis, A cy
clin-specific ubiquitinating system, including cyclin-selective ubiquitin c
arrier protein (E2-C), is thought to be responsible for cyclin B destructio
n. Here we present the cloning, sequencing and expression analaysis of gold
fish, Carassins auratus, E2-C which encodes the cyclin-selective ubiquitin
carrier protein from goldfish ovary. The cloned cDNA is 677 bp long and enc
odes 172 amino acids, The deduced amino acid sequence is highly homologous
to E2-C from other species. Recombinant goldfish E2-C possesses ubiquitinat
ing activity against cyclin B, The expression of mRNA for E2-C was similar
to that of mRNA for cyclin B, occurring at very high level in the ovary. Th
e similarity of the expression pattern of E2-C and cyclin B suggests that E
2-C mediates a cyclin-specific ubiquitination, (C) 1999 Federation of Europ
ean Biochemical Societies.