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Tissue-specific expression of p73 C-terminal isoforms in mice

Grespi, Francesca; Amelio, Ivano; Tucci, Paola; Annicchiarico-Petruzzelli, Margherita; Melino, Gerry

Authors

Francesca Grespi

Ivano Amelio

Paola Tucci

Margherita Annicchiarico-Petruzzelli

Gerry Melino



Abstract

p73 is a p53 family transcription factor. Due to the presence in the 5? flanking region of two promoters, there are two N-terminal variants, TAp73, which retains a fully active transactivation domain (TA), and ?Np73, in which the N terminus is truncated. In addition, extensive 3? splicing gives rise to at least seven distinctive isoforms; TAp73-selective knockout highlights its role as a regulator of cell death, senescence and tumor suppressor. ?Np73-selective knockout, on the other hand, highlights anti-apoptotic function of ?Np73 and its involvement in DNA damage response. In this work, we investigated the expression pattern of murine p73 C-terminal isoforms. By using a RT-PCR approach, we were able to detect mRNAs of all the C-terminal isoforms described in humans. We characterized their in vivo expression profile in mouse organs and in different mouse developmental stages. Finally, we investigated p73 C-terminal expression profile following DNA damage, ex vivo after primary cultures treatment and in vivo after systemic administration of cytotoxic compounds. Overall, our study first elucidates spatio-temporal expression of mouse p73 isoforms and provides novel insights on their expression-switch under triggered conditions.

Citation

Grespi, F., Amelio, I., Tucci, P., Annicchiarico-Petruzzelli, M., & Melino, G. (2012). Tissue-specific expression of p73 C-terminal isoforms in mice. Cell Cycle, 11(23), 4474-4483. https://doi.org/10.4161/cc.22787

Journal Article Type Article
Online Publication Date Oct 28, 2014
Publication Date 2012-12
Deposit Date Apr 1, 2020
Journal Cell Cycle
Print ISSN 1538-4101
Electronic ISSN 1551-4005
Publisher Taylor & Francis Open
Peer Reviewed Peer Reviewed
Volume 11
Issue 23
Pages 4474-4483
DOI https://doi.org/10.4161/cc.22787
Keywords C-terminal isoforms, SAM domain, cancer, development, p73
Public URL https://nottingham-repository.worktribe.com/output/4237372

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