Selective degradation of cyclins, inhibitors of cyclin-dependent kinas
es and anaphase inhibitors is responsible for several major cell cycle
transitions. The degradation of these cell cycle regulators is contro
lled by the action of target the regulators for degradation by the 26S
proteasome. Recent results indicate that two types of multisubunit ub
iquitin ligase complexes, which are connected to the protein kinase re
gulatory network of the cell cycle in different ways, are responsible
for the specific and programmed degradation of many cell cycle regulat
ors.