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Differential control of TAp73 and ΔNp73 protein stability by the ring finger ubiquitin ligase PIR2

Sayan, BS; Yang, AL; Conforti, F; Tucci, P; Piro, MC; Browne, GJ; Agostini, M; Bernardini, S; Knight, RA; Mak, TW; Melino, G

Differential control of TAp73 and ΔNp73 protein stability by the ring finger ubiquitin ligase PIR2 Thumbnail


Authors

AL Yang

F Conforti

P Tucci

MC Piro

GJ Browne

M Agostini

S Bernardini

RA Knight

TW Mak

G Melino



Abstract

p73 is a p53-related transcription factor with fundamental roles in development and tumor suppression. Transcription from two different promoters on the p73 gene results in generation of transcriptionally active TAp73 isoforms and dominant negative DeltaNp73 isoforms with opposing pro- and anti-apoptotic functions. Therefore, the relative ratio of each isoform is an important determinant of the cell fate. Proteasomal degradation of p73 is mediated by polyubiquitination-dependent and -independent processes both of which appear, thus far, to lack selectivity for the TAp73 and DeltaNp73 isoforms. Here, we describe the characterization of another transcriptional target of TAp73; a ring finger domain ubiquitin ligase p73 Induced RING 2 protein (PIR2). Although PIR2 was initially identified a p53-induced gene (p53RFP), low abundance of PIR2 transcript in mouse embryonic fibroblasts of TAp73 KO mice compared with WT mice and comparison of PIR2 mRNA and protein levels following TAp73 or p53 overexpression substantiate TAp73 isoforms as strong inducers of PIR2. Although PIR2 expression was induced by DNA damage, its expression did not alter apoptotic response or cell cycle profile per se. However, coexpression of PIR2 with TAp73 or DeltaNp73 resulted in an increase of the TA/DeltaNp73 ratio, due to preferential degradation of DeltaNp73. Finally, PIR2 was able to relieve the inhibitory effect of DeltaNp73 on TAp73 induced apoptosis following DNA damage. These results suggest that PIR2, by being induced by TAp73 and degrading DeltaNp73, differentially regulates TAp73/DeltaNp73 stability, and, hence, it may offer a therapeutic approach to enhance the chemosensitivity of tumor cells.

Citation

Sayan, B., Yang, A., Conforti, F., Tucci, P., Piro, M., Browne, G., …Melino, G. (2010). Differential control of TAp73 and ΔNp73 protein stability by the ring finger ubiquitin ligase PIR2. Proceedings of the National Academy of Sciences, 107(29), https://doi.org/10.1073/pnas.0911828107

Journal Article Type Article
Publication Date Jul 20, 2010
Deposit Date Feb 7, 2023
Publicly Available Date Feb 7, 2023
Journal Proceedings of the National Academy of Sciences
Electronic ISSN 1091-6490
Publisher National Academy of Sciences
Volume 107
Issue 29
DOI https://doi.org/10.1073/pnas.0911828107
Publisher URL https://doi.org/10.1073/pnas.0911828107

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