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Murine PIRH2 (mPIRH2) was recently identified as a RING finger-containing ubiquitin-protein isopeptide ligase that interacts with both p53 and the human androgen receptor. mpirh2 is a p53-responsive gene that is up-regulated by UV, and mPIRH2 protein has the capacity to polyubiquitylate p53, perhaps leading to p53 destruction. mpirh2 therefore has properties similar to those of the oncogene mdm2. Here, we have identified human PIRH2 (hPIRH2) as a TIP60-interacting protein. To investigate its regulation, we characterized hPIRH2 in parallel with hPIRH2 variants possessing mutations of conserved RING finger residues. We observed that wild-type hPIRH2 is an unstable protein with a short half-life and is a target for RING domain-dependent proteasomal degradation. Accordingly, we found that hPIRH2 was ubiquitylated in cells. The TIP60-hPIRH2 association appeared to regulate hPIRH2 stability; coexpression of TIP60 enhanced hPIRH2 protein stability and altered hPIRH2 subcellular localization. These results suggest that hPIRH2 activities can be controlled, at the post-translational level, in multiple ways.

Original publication




Journal article


J Biol Chem

Publication Date





11696 - 11704


Acetyltransferases, Amino Acid Sequence, Animals, Base Sequence, Cell Line, Cysteine Endopeptidases, DNA Primers, Histone Acetyltransferases, Humans, Lysine Acetyltransferase 5, Molecular Sequence Data, Multienzyme Complexes, Proteasome Endopeptidase Complex, Protein Binding, Protein Processing, Post-Translational, Two-Hybrid System Techniques, Ubiquitin-Protein Ligases