Abstract
Integrated HIV-1 genomes are found within actively transcribed host genes in latently infected CD4+ T cells. Readthrough transcription of the host gene might therefore suppress HIV-1 gene expression and promote the latent infection that allows viral persistence in patients on therapy. To address the effect of host gene readthrough, we used homologous recombination to insert HIV-1 genomes in either orientation into an identical position within an intron of an actively transcribed host gene, hypoxanthine-guanine phosphoribosyltransferase (HPRT). Constructs were engineered to permit or block readthrough transcription of HPRT. Readthrough transcription inhibited HIV-1 gene expression for convergently orientated provirus but enhanced HIV-1 gene expression when HIV-1 was in the same orientation as the host gene. Orientation had a >10-fold effect on HIV-1 gene expression. Due to the nature of HIV-1 integration sites in vivo, this orientation-dependent regulation can influence the vast majority of infected cells and adds complexity to the maintenance of latency.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 134-146 |
| Number of pages | 13 |
| Journal | Cell Host and Microbe |
| Volume | 4 |
| Issue number | 2 |
| DOIs | |
| State | Published - Aug 14 2008 |
Keywords
- MICROBIO
- MOLIMMUNO
ASJC Scopus subject areas
- Parasitology
- Microbiology
- Virology
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