Journal of Leukocyte Biology
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A more recent version of this article appeared on September 1, 2006

Published online before print July 14, 2006
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© by The Society for Leukocyte Biology
Journal of Leukocyte Biology, doi:10.1189/jlb.0306189


Received for publication March 13, 2006.
Revised May 2, 2006.
Accepted for publication May 11, 2006.


Article

Inhibition of HIV-1 replication by RNA interference of p53 expression

Eduardo Pauls , Jordi Senserrich , Bonaventura Clotet , and Jose A. Esté @

Retrovirology Laboratory irsiCaixa, Hospital Universitari Germans Trias i Pujol, Universitat Autònoma de Barcelona, Spain

@ To whom correspondence should be addressed. E-mail: jaeste{at}irsicaixa.es.


   Abstract

p53 expression and activation have been associated to faster human immunodeficiency virus (HIV) disease progression, most probably by inducing CD4+ T cell death but also through its cooperative effect in the control of viral gene transcription by viral regulatory proteins. Here, we show that RNA interference of p53 in HIV-1 reporter (HeLa P4-R5 MAGI) and lymphoid (SupT1) cell lines blocked HIV-1 and Tat-induced transcription from the HIV-1 promoter and HIV-1 replication in acutely infected cells, suggesting a cooperative role of p53 in HIV-1 transcription. Contrary to SupT1 cells, which encode several mutations on the p53 DNA binding domain, death of HIV-1-induced syncytia was reduced in cocultures of HeLa P4-R5 MAGI with persistently infected HIV-1 cells. To our knowledge, this is the first demonstration of the effect of the loss of function of p53 in HIV-1 replication, which is independent on its classical DNA binding activity. Our results suggest two independent roles for p53 in HIV-1 infection: cooperation in HIV long-terminal repeat transcription and virus-induced cell death.

Key Words: transcription • MAGI • SupT1




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S.-S. Chang, Y.-C. Lo, H.-H. Chua, H.-Y. Chiu, S.-C. Tsai, J.-Y. Chen, K.-W. Lo, and C.-H. Tsai
Critical Role of p53 in Histone Deacetylase Inhibitor-Induced Epstein-Barr Virus Zta Expression
J. Virol., August 1, 2008; 82(15): 7745 - 7751.
[Abstract] [Full Text] [PDF]




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