1. Academic Validation
  2. The F-box protein FBXO45 promotes the proteasome-dependent degradation of p73

The F-box protein FBXO45 promotes the proteasome-dependent degradation of p73

  • Oncogene. 2009 Sep 3;28(35):3157-66. doi: 10.1038/onc.2009.177.
A Peschiaroli 1 F Scialpi F Bernassola M Pagano G Melino
Affiliations

Affiliation

  • 1 IDI-IRCCS Biochemistry Laboratory, Department of Experimental Medicine and Biochemical Sciences, University of Rome Tor Vergata, Rome 00133, Italy.
Abstract

The transcription factor p73, a member of the p53 family, mediates cell-cycle arrest and Apoptosis in response to DNA damage-induced cellular stress, acting thus as a proapoptotic gene. Similar to p53, p73 activity is regulated by post-translational modification, including phosphorylation, acetylation and ubiquitylation. In C. elegans, the F-box protein FSN-1 controls germline Apoptosis by regulating CEP-1, the single ancestral p53 family member. Here we report that FBXO45, the human ortholog of FSN-1, binds specifically to p73 triggering its proteasome-dependent degradation. Importantly, SCF(FBXO45) ubiquitylates p73 both in vivo and in vitro. Moreover, siRNA-mediated depletion of FBXO45 stabilizes p73 and concomitantly induces cell death in a p53-independent manner. All together, these results show that the orphan F-box protein FBXO45 regulates the stability of p73, highlighting a conserved pathway evolved from nematode to human by which the p53 members are regulated by an SCF-dependent mechanism.

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