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Purification of anaphase promoting complex/cyclosome from goldfish oocytes
Authors:T. Tokumoto  M. Tokumoto  M. Ishimatsu  R. Horiguchi  Y. Nagahama  K. Ishikawa
Affiliation:1. Department of Biology and Geosciences, Faculty of Science, Shizuoka University, Shizuoka, 422, Japan
2. CREST Research Project, Japan Science and Technology Corporation, Japan
3. National Institute for Basic Biology, Okazaki, 444, Japan
Abstract:Destruction of cyclin B is required for exit from mitosis and meiosis. A cyclin-specific ubiquitinating system, including anaphase-promoting complex/cyclosome (APC/C) is thought to be responsible for cyclin B destruction. To learn more about the molecular mechanism of cyclin B degradation, a molecular study of the ubiquitinating system in goldfish has been undertaken. For biochemical preparation of APC/C, we first conducted the cloning, sequencing and expression analysis of goldfish, Carassius auratus, cdc27 that encodes a subunit of APC/C from goldfish ovary. The deduced amino acid sequence is highly homologous to cdc27 from other species. Then recombinant goldfish Cdc27CT (C-terminal half of Cdc27) was expressed in Escherichia coli, and an antibody was raised against purified recombinant protein. Polyclonal antiserum cross-reactive with Cdc27 was obtained. By the assay using the antibody, APC/C was purified by column chromatographs.
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