HOPS/TMUB1 retains p53 in the cytoplasm and sustains p53-dependent mitochondrial apoptosis

ABSTRACT: Apoptotic signalling by p53 occurs at both transcriptional and non-transcriptional levels, as p53 may act as a direct apoptogenic stimulus via activation of the intrinsic mitochondrial pathway. HOPS is a highly conserved, ubiquitously expressed shuttling protein with an ubiquitin-like domain. We generated Hops?/? mice and observed that they are viable with no apparent phenotypic defects. However, when treated with chemotherapeutic agents, Hops?/? mice display a significant reduction in apoptosis, suggesting an impaired ability to respond to genotoxic stressors. We show that HOPS acts as a regulator of cytoplasmic p53 levels and function. By binding p53, HOPS inhibits p53 proteosomal degradation and favours p53 recruitment to mitochondria and apoptosis induction. By interfering with importi

SUBMITTER: Prof. Giuseppe Servillo 

PROVIDER: S-SCDT-EMBOR-2019-48073-T | biostudies-other |

REPOSITORIES: biostudies-other