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Human foamy virus genome possesses an internal, Bel-1-dependent and functional promoter.
| Content Provider | Semantic Scholar |
|---|---|
| Author | Löchelt, Martin Muranyi, Walter Flügel, Rolf M. |
| Copyright Year | 1993 |
| Abstract | The human foamy or spumaretrovirus (HSRV) is a complex retrovirus that encodes the three retroviral genes gag, pol, and env and, in addition, at least three bel genes. The HSRV Bel-1 protein was identified as a transcriptional trans-activator. HSRV transcription starts in the 5' long terminal repeat at a defined guanine residue. We report here that a second efficiently utilized start site of transcription is contained within a HSRV env DNA sequence upstream of the bel genes. Bel-specific transcripts that initiate at the internal transcriptional start site at nt 9196 were identified in HSRV-infected cells by primer extension and S1 nuclease analysis, and the intragenic promoter was shown to be constitutively activated by Bel-1 in the HSRV provirus. In transient expression assays with indicator gene constructs, expression by the HSRV intragenic promoter/enhancer is Bel-1 dependent. The data provide evidence for an intragenic start site of transcription in the genome of a complex, exogenous human retrovirus and are discussed in terms of a model for regulating spumaretroviral gene expression. |
| Starting Page | 293 |
| Ending Page | 300 |
| Page Count | 8 |
| File Format | PDF HTM / HTML |
| Alternate Webpage(s) | http://www.pnas.org/content/90/15/7317.full.pdf |
| PubMed reference number | 8394017v1 |
| Volume Number | 90 |
| Issue Number | 15 |
| Journal | Proceedings of the National Academy of Sciences of the United States of America |
| Language | English |
| Access Restriction | Open |
| Subject Keyword | Contain (action) Enhancer of transcription Gene Expression Guanine Long Terminal Repeat Primer Extension Proviruses Retroviridae Spumavirus Terminal Repeat Sequences Trans-Activators Transcript Transcription, Genetic nuclease |
| Content Type | Text |
| Resource Type | Article |