Abstract / Description of output
Transcription from the human cytomegalovirus major immediate-early promoter is dependent on host-cell regulatory proteins. The interactions between cellular nuclear proteins and a unique sequence located from nucleotide position -660 to -540 was investigated. The unique region presents a defined target for multiple distinct DNA-binding proteins which appear, in part, to have overlapping binding sites. A minimum of five sequence-specific DNA-binding activities that interact with sequences between -632 and -602, -602 and -557, -602 and -590, -563 and -540, and -602 and -582 were detected. Evidence is presented to suggest that the -632 to -602 site, a previously characterized nuclear factor 1 binding site, does not bind NF1 but strongly interacts with a distinct cellular factor. The binding of cellular proteins to the unique sequence region was shown to be important in directing transcription from the major immediate-early promoter.
Original language | English |
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Pages (from-to) | 18-25 |
Number of pages | 8 |
Journal | Journal of Virology |
Volume | 174 |
Issue number | 1 |
Publication status | Published - 1990 |
Keywords / Materials (for Non-textual outputs)
- Antigens, Viral
- Base Sequence
- Binding Sites
- Chromatography
- Cytomegalovirus
- DNA, Viral
- DNA-Binding Proteins
- HeLa Cells
- Humans
- Immediate-Early Proteins
- Molecular Sequence Data
- Nuclear Proteins
- Promoter Regions, Genetic
- Transcription Factors
- Transcription, Genetic
- Transfection