Abstract
Cyclin F, a cyclin that can form SCF complexes and bind to cyclin B, oscillates in the cell cycle with a pattern similar to cyclin A and cyclin B. Ectopic expression of cyclin F arrests the cell cycle in G(2)/M. How the level of cyclin F is regulated during the cell cycle is completely obscure. Here we show that, similar to cyclin A, cyclin F is degraded when the spindle assembly checkpoint is activated and accumulates when the DNA damage checkpoint is activated. Cyclin F is a very unstable protein throughout much of the cell cycle. Unlike other cyclins, degradation of cyclin F is independent of ubiquitination and proteasome-mediated pathways. Interestingly, proteolysis of cyclin F is likely to involve metalloproteases. Rapid destruction of cyclin F does not require the N-terminal F-box motif but requires the COOH-terminal PEST sequences. The PEST region alone is sufficient to interfere with the degradation of cyclin F and confer instability when fused to cyclin A. These data show that although cyclin F is degraded at similar time as the mitotic cyclins, the underlying mechanisms are entirely distinct.
Original language | English |
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Pages (from-to) | 35140-35149 |
Number of pages | 10 |
Journal | Journal of Biological Chemistry |
Volume | 277 |
Issue number | 38 |
DOIs | |
Publication status | Published - 20 Sept 2002 |
Keywords
- Cell Line
- Cyclins
- DNA Damage
- G2 Phase
- Humans
- Hydrolysis
- Mitosis
- Recombinant Proteins
- S Phase