| Literature DB >> 10078201 |
J K Hsieh1, F S Chan, D J O'Connor, S Mittnacht, S Zhong, X Lu.
Abstract
The binding of RB to MDM2 is shown to be essential for RB to overcome both the antiapoptotic function of MDM2 and the MDM2-dependent degradation of p53. The RB-MDM2 interaction does not prevent MDM2 from inhibiting p53-dependent transcription, but the RB-MDM2 complex still binds to p53. Since RB specifically rescues the apoptotic function but not the transcriptional activity of p53 from negative regulation by MDM2, transactivation by wild-type p53 is not required for the apoptotic function of p53. However, an RB-MDM2-p53 trimeric complex is active in p53-mediated transrepression. These data link directly the function of two tumor suppressor proteins and demonstrate a novel role of RB in regulating the apoptotic function of p53.Entities:
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Year: 1999 PMID: 10078201 DOI: 10.1016/s1097-2765(00)80309-3
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970