Abstract / Description of output
The effect of the human cytomegalovirus immediate early region 1 enhancer on transcription was studied in vitro with HeLa cell nuclear extract. Stimulation of in vitro transcription mediated by the enhancer element involves its recognition by specific trans-acting factors present in the nuclear extract. DNase I protection analysis was used to determine at the nucleotide level those enhancer sequences that interact with nuclear factors. At least nine sites of protein-DNA interaction were detected over approximately 400 base pairs of enhancer sequence. The regions of nuclease protection are associated with 21-, 19-, 18-, and 17-base-pair repeat elements as well as with a unique sequence, creating a large nucleoprotein complex. The relationship between the protein binding and the activity of the immediate early region 1 enhancer is discussed.
Original language | English |
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Pages (from-to) | 3658-62 |
Number of pages | 5 |
Journal | Proceedings of the National Academy of Sciences (PNAS) |
Volume | 84 |
Issue number | 11 |
DOIs | |
Publication status | Published - 1987 |
Keywords / Materials (for Non-textual outputs)
- Base Sequence
- Cell Nucleus
- Cytomegalovirus
- Enhancer Elements, Genetic
- Genes
- Genes, Regulator
- Genes, Viral
- HeLa Cells
- Humans
- Plasmids
- Promoter Regions, Genetic
- Templates, Genetic
- Transcription Factors
- Transcription, Genetic