Abstract |
The immediate-early 1 and 2 gene locus of human cytomegalovirus (HCMV) that encodes trans-activator proteins with effects on both homologous and heterologous promoters is expressed under control of a complex enhancer/promoter regulatory region. This enhancer contains four types of repetitive sequence elements with 17, 18, 19, and 21 bp that bind cellular transcription factors. Although the HCMV enhancer acts as a powerful stimulator of transcription in most cell types examined, human T cells do not support strong activity. The present study demonstrates that the tax gene product of human T-cell leukemia virus type I trans activates the major enhancer of HCMV more than 60-fold in the T-cell line Jurkat. When a series of chloramphenicol acetyltransferase expression plasmids containing synthetic oligonucleotides with the 17-, 18-, 19-, or 21-bp motif upstream of a minimal immediate-early 1 and 2 gene promoter was tested, two of the four repeat motifs could be identified as Tax-responsive elements. Both the 18- and the 19-bp motifs were able to act as strong Tax-responsive elements even when they were present as single copies. Thus, in addition to interacting with human immunodeficiency virus, HCMV is able to interact with a second retrovirus of clinical importance.
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Authors | H Moch, D Lang, T Stamminger |
Journal | Journal of virology
(J Virol)
Vol. 66
Issue 12
Pg. 7346-54
(Dec 1992)
ISSN: 0022-538X [Print] United States |
PMID | 1331524
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Gene Products, tax
- RNA, Viral
- Chloramphenicol O-Acetyltransferase
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Topics |
- Avian Sarcoma Viruses
(genetics)
- Base Sequence
- Chloramphenicol O-Acetyltransferase
(genetics, metabolism)
- Cloning, Molecular
- Cytomegalovirus
(genetics)
- Enhancer Elements, Genetic
- Gene Expression Regulation, Viral
- Gene Products, tax
(genetics, metabolism)
- Genes, pX
- Human T-lymphotropic virus 1
(genetics)
- Humans
- Molecular Sequence Data
- Plasmids
- RNA, Viral
(genetics, isolation & purification)
- Repetitive Sequences, Nucleic Acid
- T-Lymphocytes
- Transcription, Genetic
- Transcriptional Activation
- Transfection
- Tumor Cells, Cultured
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