This article is part of the supplement: Frontiers of Retrovirology: Complex retroviruses, retroelements and their hosts
Invited speaker presentation
The ups and downs of HIV-1 gene expression
Retrovirology 2009, 6(Suppl 2):I11 doi:10.1186/1742-4690-6-S2-I11
The electronic version of this article is the complete one and can be found online at: http://www.retrovirology.com/content/6/S2/I11
| Published: | 24 September 2009 |
© 2009 Kiernan; licensee BioMed Central Ltd.
Invited speaker presentation
Following infection, Human Immunodeficiency Virus type 1 (HIV-1) becomes stably integrated into the genome of the host cell. It depends, therefore, on host cell factors to regulate its transcriptional output, both positively and negatively. HIV-1 transcriptional silencing requires chromatin remodelling and transcriptional repressor complexes, as well as heterochromatin formation at the integrated provirus. An important feature of silenced proviruses is their ability to be re-activated by either the viral transcription factor, Tat, or environmental stimuli. Activation of transcription is also controlled by numerous host cell factors. We have identified novel mechanisms of transcriptional activation and repression that depend on cellular macromolecular complexes such as proteasome and nuclear exosome. I will discuss recent developments in understanding the mechanisms by which these complexes control HIV-1 transcription, and the implications for viral latency.