FKBP25, a novel regulator of the p53 pathway, induces the degradation of MDM2 and activation of p53

The p53 tumour suppressor protein is tightly controlled by the E3 ubiquitin ligase, mouse double minute 2 (MDM2), but maintains MDM2 expression as part of a negative feedback loop. We have identified the immunophilin, 25 kDa FK506-binding protein (FKBP25), previously shown to be regulated by p53-mediated repression, as an MDM2-interacting partner. We show that FKBP25 stimulates auto-ubiquitylation and proteasomal degradation of MDM2, leading to the induction of p53. Depletion of FKBP25 by siRNA leads to increased levels of MDM2 and a corresponding reduction in p53 and p21 levels. These data are consistent with the idea that FKBP25 contributes to regulation of the p53-MDM2 negative feedback loop. MINT- 6823686: MDM2 (uniprotkb: Q00987) physically interacts (MI: 0218) with FKBP25 (uniprotkb: Q00688) by anti bait coimmunoprecipitation (MI: 0006) MINT- 6823707, MINT- 6823722: MDM2 (uniprotkb: Q00987) physically interacts (MI: 0218) with FKBP25 (uniprotkb: Q62446) by pull down (MI: 0096) MINT- 6823775: P53 (uniprotkb: Q04637) physically interacts (MI: 0218) with MDM2 (uniprotkb: Q00987) by anti bait coimmunoprecipitation (MI: 0006) MINT- 6823735, MINT- 6823749: FKBP25 (uniprotkb: Q62446) binds (MI: 0407) to MDM2 (uniprotkb: Q00987) by pull down (MI: 0096) MINT- 6823761: Ubiquitin (UNIPROTKB: 62988)P physically interacts (MI: 0218) with MDM2 (uniprotkb: Q00987) by pull down (MI: 0096) MINT- 6823669: MDM2 (uniprotkb: Q00987) physically interacts (MI: 0218) with FKBP25 (uniprotkb: Q00688) by two hybrid (MI: 0018)