Abstract
The role of cyclin B-CDC2 as M phase-promoting factor (MPF) is well established, but the precise functions of cyclin A remain a crucial outstanding issue. Here we show that down-regulation of cyclin A induces a G2 phase arrest through a checkpoint-independent inactivation of cyclin B-CDC2 by inhibitory phosphorylation. The phenotype is rescued by expressing cyclin A resistant to the RNA interference. In contrast, down-regulation of cyclin B disrupts mitosis without inactivating cyclin A-CDK, indicating that cyclin A-CDK acts upstream of cyclin B-CDC2. Even when ectopically expressed, cyclin A cannot replace cyclin B in driving mitosis, indicating the specific role of cyclin B as a component of MPF. Deregulation of WEE1, but not the PLK1-CDC25 axis, can override the arrest caused by cyclin A knockdown, suggesting that cyclin A-CDK may tip the balance of the cyclin B-CDC2 bistable system by initiating the inactivation of WEE1. These observations show that cyclin A cannot form MPF independent of cyclin B and underscore a critical role of cyclin A as a trigger for MPF activation.
Original language | English |
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Pages (from-to) | 1861-1873 |
Number of pages | 13 |
Journal | Mol Biol Cell |
Volume | 18 |
Issue number | 5 |
DOIs | |
Publication status | Published - May 2007 |
Keywords
- Base Sequence
- CDC2 Protein Kinase
- Cell Cycle Proteins
- Cyclin A
- Cyclin B
- DNA Primers
- Down-Regulation
- G2 Phase
- HeLa Cells
- Humans
- Maturation-Promoting Factor
- Mitosis
- Models, Biological
- Nuclear Proteins
- Phosphorylation
- Protein-Serine-Threonine Kinases
- Protein-Tyrosine Kinases
- Proto-Oncogene Proteins
- RNA Interference
- cdc25 Phosphatases