PML regulates p53 stability by sequestering Mdm2 to the nucleolus.

The promyelocytic leukaemia (PML) tumour-suppressor protein potentiates p53 function by regulating post-translational modifications, such as CBP-dependent acetylation and Chk2-dependent phosphorylation, in the PML-Nuclear Body (NB). PML was recently shown to interact with the p53 ubiquitin-ligase Mdm2 (refs 4-6); however, the mechanism by which PML regulates Mdm2 remains unclear. Here, we ...
show that PML enhances p53 stability by sequestering Mdm2 to the nucleolus. We found that after DNA damage, PML and Mdm2 accumulate in the nucleolus in an Arf-independent manner. In addition, we found that the nucleolar localization of PML is dependent on ATR activation and phosphorylation of PML by ATR. Notably, in Pml(-/-) cells, sequestration of Mdm2 to the nucleolus was impaired, as well as p53 stabilization and the induction of apoptosis. Furthermore, we demonstrate that PML physically associates with the nucleolar protein L11, and that L11 knockdown impairs the ability of PML to localize to nucleoli after DNA damage. These findings demonstrate an unexpected role of PML in the nucleolar network for tumour suppression.
Mesh Terms:
ADP-Ribosylation Factor 1, Active Transport, Cell Nucleus, Animals, Cell Compartmentation, Cell Cycle Proteins, Cell Line, Transformed, Cell Nucleolus, Cells, Cultured, Fibroblasts, Humans, Mice, NIH 3T3 Cells, Neoplasm Proteins, Nuclear Proteins, Phosphorylation, Protein Transport, Protein-Serine-Threonine Kinases, Proto-Oncogene Proteins, Proto-Oncogene Proteins c-mdm2, RNA Stability, Ribosomal Proteins, Transcription Factors, Tumor Suppressor Protein p53, Tumor Suppressor Proteins
Nat. Cell Biol.
Date: Jul. 01, 2004
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