Proteolysis and the cell cycle
- PMID: 12429938
- DOI: 10.4161/cc.1.4.130
Proteolysis and the cell cycle
Abstract
Without doubt, one of the more dramatic breakthroughs in recent cell cycle history has been the discovery that growth regulators are controlled by proteolysis. This concept blossomed within the last six or seven years, but the story really began when cyclins were discovered, soon followed by the suggestion that proteolysis events might control cell cycle transitions. Proteolytic targets that are now known include most of the cyclins, cyclin dependent kinase inhibitors, DNA replication factors, the securin class of proteins that inhibit loss of sister chromatid cohesion following DNA replication and, of course, the cohesion factor itself. Protein degradation is controlled in various ways including ubiquitin-dependent targeting to proteasomes, activation of ubiquitin ligases by ubiquitin-like molecule conjugation, phosphorylation of proteolytic targets, and activation of the separin class of proteases.
Comment on
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SUMO-1 and p53.Cell Cycle. 2002 Jul-Aug;1(4):245-9. Cell Cycle. 2002. PMID: 12429940 Review.
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Seek and destroy: SCF ubiquitin ligases in mammalian cell cycle control.Cell Cycle. 2002 Jul-Aug;1(4):250-4. Cell Cycle. 2002. PMID: 12429941 Review.
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Mitotic regulation: the fine tuning of separase activity.Cell Cycle. 2002 Jul-Aug;1(4):255-7. Cell Cycle. 2002. PMID: 12429942 Review.
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