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Papers In Press, published online ahead of print November 21, 2001
J. Biol. Chem, 10.1074/jbc.M109491200
Submitted on October 2, 2001
Revised on November 21, 2001
Accepted on November 21, 2001

PATZ attenuates the RNF4-mediated enhancement of AR-dependent transcription

Raffaela Pero, Francesca Lembo, Emiliano Antonio Palmieri, Carmen Vitiello, Monica Fedele, Alfredo Fusco, Carmelo Bruno Bruni, and Lorenzo Chiariotti

Biologia e Patologia Cellulare e Molecolare, Università di Napoli, Naples 80131

Corresponding Author: chiariot{at}unina.it

PATZ is a transcriptional repressor affecting the basal activity of different promoters whereas RNF4 is a transcriptional activator. The association of PATZ with RNF4 switches activation to repression of selected basal promoters. Because RNF4 interacts also with the androgen receptor (AR) functioning as a coactivator and, in turn, RNF4 associates with PATZ, we investigated whether PATZ functions as an AR coregulator. We demonstrate that PATZ does not influence directly the AR response but acts as an AR corepressor in the presence of RNF4. Such repression is not dependent on histone deacetylases. A mutant RNF4 that does not bind PATZ, but enhances AR-dependent transcription is not influenced by PATZ demonstrating that the repression by PATZ occurs only upon binding to RNF4. We also demonstrate that RNF4, AR and PATZ belong to the same complex in vivo, also in the presence of androgen, suggesting that repression is not mediated by the displacement of RNF4 from AR. Finally, we show that repression of endogenous PATZ expression by antisense expression plasmids in LNCaP cells, results in a stronger androgen response. Our findings demonstrate that PATZ is a novel AR coregulator that acts by modulating the effect of a coactivator. This could represent a novel, more general, mechanism to finely tune the androgen response.


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