Nucleic Acids Research, 1992, Vol. 20, No. 16 4129-4136
© 1992
MOLECULAR BIOLOGY |
Identification of regulatory elements within the minimal promoter region of the human endogenous ERV9 proviruses: accurate transcription initiation is controlled by an Inr-like element
Department of Genetics, General and Molecular Biology, University of Nalpes Via Mezzocannone 8, 80134 Naples 1International Institute of Genetics and Biophysics CNR, Naples, Italy
Received July 2, 1992. Accepted July 23, 1992.
ERV9 is a low repeated family of human endogenous retroviral elements whose expression Is mainly detectable in undifferentiated embryonal carcinoma NT2/D1 cells. In this report we have analyzed the minimal promoter region located within the ERV9 LTR. Using the transient CAT expression assay we have identified the minimal promoter region, which includes sequences spanning from 70 to +6 relative to the major transcription start site. Deletion analysis, primer extension mapping of the transcription start sites and DNA-proteln interactions assays have allowed us to define two important regions within the ERV9 minimal promoter. One region located between 70 to 39 acts as a transcriptional activating sequence and contains an Sp1 binding site. The second region from 7 to +6, which resembles an initiator element (Inr), was necessary for the correct transcription start site utilization, and binds to a regulatory protein. Crosscompetition experiments using various Inr elements have indicated that the protein that binds to the ERV9 Inr element can be competed by the HIV1 and TdT Inr sequences.
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