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Integrin-β4 is a novel transcriptional target of TAp73

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Version 2 2018-02-08, 13:31
Version 1 2017-12-13, 08:41
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posted on 2018-02-08, 13:31 authored by Ningxia Xie, Polina Vikhreva, Margherita Annicchiarico-Petruzzelli, Ivano Amelio, Nicolai Barlev, Richard A. Knight, Gerry Melino

As a member of p53 family, p73 has attracted intense investigations due to its structural and functional similarities to p53. Among more than ten p73 variants, the transactivation (TA) domain-containing isoform TAp73 is the one that imitates the p53's behavior most. TAp73 induces apoptosis and cell cycle arrest, which endows it the capacity of tumour suppression. Also, it can exert diverse biological influences on cells through activating a complex and context dependent transcriptional programme. The transcriptional activities further broaden its roles in more intricate biological processes. In this article, we report that p73 is a positive regulator of a cell adhesion related gene named integrin β4 (ITGB4). This finding may have implications for the dissection of the biological mechanisms underlining p73 functions.

Funding

This study was supported by the Medical Research Council, United Kingdom, by Associazione Italiana per la Ricerca contro il Cancro (AIRC): AIRC 2014 IG15653 (to G.M.), AIRC 5xmille MCO9979 (to G.M.) and AIRC 2011 IG11955 (to G.M.). G.M. and N.B. also acknowledge the support of RSF grant# 14-50-00068.

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