Publication | Open Access
Dissociation of retinoblastoma gene protein hyperphosphorylation and commitment to enter S phase
12
Citations
77
References
1994
Year
Viral ReplicationMolecular RegulationImmunologyMolecular BiologyAntigen ProcessingCell CycleS PhaseImmunotherapyCellular PhysiologyCell RegulationVirus GeneCell SignalingPrb BindingCell DivisionDna ReplicationVirologyGene ExpressionCell BiologyProtein PhosphorylationSignal TransductionNatural SciencesMitogenic ActivitiesCellular BiochemistryMedicine
Mitogenic activities of simian virus 40 large T and small t antigens were studied in serum-deprived human diploid fibroblasts. Wild-type large T and small t cooperated in stimulating DNA synthesis and in inducing hyperphosphorylation of the Rb gene product (pRb). In contrast, a T antigen mutant defective for pRb binding (Rb- T) possessed no detectable mitogenic activity alone and failed to complement small t in stimulating DNA synthesis. Surprisingly, Rb- T and small t cooperated as strongly as wild-type T and small t with respect to pRb hyperphosphorylation. As a consequence, in two closely related conditions (i.e., stimulation by small t plus wild-type T versus small t plus Rb- T), the fraction of pRb in hyperphosphorylated forms dissociated from the fraction of cells in the S phase. These results indicate that pRb hyperphosphorylation is not always tightly coupled with a commitment to initiate DNA replication.
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