Chromatin-associated regulation of HIV-1 transcription: implications for the development of therapeutic strategies
- PMID: 17484137
Chromatin-associated regulation of HIV-1 transcription: implications for the development of therapeutic strategies
Abstract
Human Immunodeficiency Virus type 1 (HIV-1) infection can now be treated effectively in many patients in the developed world, using combinations of antiretroviral therapeutics, called Highly Active Anti-Retroviral Therapy (HAART). However, despite prolonged treatment with HAART, the persistence of latently HIV-1-infected cellular reservoirs harboring transcriptionally silent but replication-competent proviruses represents the major hurdle to virus eradication. These latently infected cells are a permanent source for virus reactivation and lead to a rebound of the viral load after interruption of HAART. Therefore, a greater understanding of the molecular mechanisms regulating proviral latency and reactivation should lead to rational strategies aimed at purging these cellular reservoirs of HIV-1. This review summarizes our current knowledge and understanding of the elements involved in HIV-1 transcriptional reactivation: (1) the site of integration; (2) the transcription factor NF-kappaB, which is induced by proinflammatory cytokines (such as TNFalpha) and binds to two kappaB sites in the HIV-1 promoter region; (3) the specific remodeling of a single nucleosome (called nuc-1 and located immediately downstream of the HIV-1 transcription start site under latency conditions) upon activation of the HIV-1 promoter; (4) post-translational acetylation of histones and of non-histone proteins (following treatment with deacetylases inhibitors, which induce viral transcription and nuc-1 remodeling); and (5) the viral trans-activator Tat, which promotes transcription by mediating the recruitment to the HIV-1 promoter of histone-modifying enzymes and ATP-dependent chromatin remodeling complexes required for nucleosome disruption and transcriptional processivity. Finally, this review highlights experimental therapies aimed at administrating HIV-1 gene expression activators (such as HDAC inhibitors) combined with an effective HAART in order to reactivate and decrease/eliminate the pool of latently HIV-1-infected cellular reservoirs
Similar articles
-
Molecular mechanisms involved in HIV-1 transcriptional latency and reactivation: implications for the development of therapeutic strategies.Bull Mem Acad R Med Belg. 2004;159(Pt 2):176-89. Bull Mem Acad R Med Belg. 2004. PMID: 15615091 Review.
-
NF-kappaB p50 promotes HIV latency through HDAC recruitment and repression of transcriptional initiation.EMBO J. 2006 Jan 11;25(1):139-49. doi: 10.1038/sj.emboj.7600900. Epub 2005 Dec 1. EMBO J. 2006. PMID: 16319923 Free PMC article.
-
Administration of HDAC inhibitors to reactivate HIV-1 expression in latent cellular reservoirs: implications for the development of therapeutic strategies.Biochem Pharmacol. 2004 Sep 15;68(6):1231-8. doi: 10.1016/j.bcp.2004.05.040. Biochem Pharmacol. 2004. PMID: 15313421 Review.
-
Inhibition of human immunodeficiency virus type 1 transcription by N-aminoimidazole derivatives.Virology. 2007 Aug 15;365(1):220-37. doi: 10.1016/j.virol.2007.03.036. Epub 2007 Apr 24. Virology. 2007. PMID: 17459445
-
Epigenetic regulation of HIV-1 transcription.Epigenomics. 2011 Aug;3(4):487-502. doi: 10.2217/epi.11.61. Epigenomics. 2011. PMID: 22126207 Review.
Cited by
-
Synergistic activation of HIV-1 expression by deacetylase inhibitors and prostratin: implications for treatment of latent infection.PLoS One. 2009 Jun 30;4(6):e6093. doi: 10.1371/journal.pone.0006093. PLoS One. 2009. PMID: 19564922 Free PMC article.
-
Impact of Chromatin on HIV Replication.Genes (Basel). 2015 Sep 30;6(4):957-76. doi: 10.3390/genes6040957. Genes (Basel). 2015. PMID: 26437430 Free PMC article. Review.
-
A limited group of class I histone deacetylases acts to repress human immunodeficiency virus type 1 expression.J Virol. 2009 May;83(10):4749-56. doi: 10.1128/JVI.02585-08. Epub 2009 Mar 11. J Virol. 2009. PMID: 19279091 Free PMC article.
-
Toll-like receptor-3 mediates HIV-1 transactivation via NFκB and JNK pathways and histone acetylation, but prolonged activation suppresses Tat and HIV-1 replication.Cell Signal. 2016 Feb;28(2):7-22. doi: 10.1016/j.cellsig.2015.11.005. Epub 2015 Nov 11. Cell Signal. 2016. PMID: 26569339 Free PMC article.
-
Poly(ADP-ribose) polymerase 1 promotes transcriptional repression of integrated retroviruses.J Virol. 2013 Mar;87(5):2496-507. doi: 10.1128/JVI.01668-12. Epub 2012 Dec 19. J Virol. 2013. PMID: 23255787 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources
Miscellaneous