Sequence specific binding of the transcription factor c-Ets1 to the human immunodeficiency virus type I long terminal repeat

Biochem Biophys Res Commun. 1993 Dec 30;197(3):1229-33. doi: 10.1006/bbrc.1993.2608.

Abstract

Human immunodeficiency virus type I (HIV-1) long terminal repeat (LTR) driven transcription is regulated by a variety of cellular transcription factors. Most work has focused on the two nuclear factor kappa B (NF-kB) elements indispensable for HIV-1 LTR enhancer function. We demonstrate here the specific binding of the transcription factor c-Ets1 to an U3 region of the HIV-1 LTR (nt -141 to -149) using electrophoretic mobility shift analysis with T-cell nuclear extract and in vitro translated protein. This previously not identified Ets binding site is highly conserved among different HIV-1 isolates and maps to an U3 region recently shown to be necessary for viral growth in vitro. The c-Ets proto-oncogene family of transcription factors has yet been associated with HTLV-I and HIV-2 transcription. Our present analysis suggests an important role of c-Ets proteins in HIV-1 transcription.

Publication types

  • Comparative Study

MeSH terms

  • Base Sequence
  • Cell Line
  • Cell Nucleus / metabolism
  • HIV Long Terminal Repeat*
  • HIV-1 / genetics
  • HIV-1 / metabolism*
  • Humans
  • Molecular Sequence Data
  • Nuclear Proteins / metabolism
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma
  • Protein Biosynthesis
  • Proto-Oncogene Mas
  • Proto-Oncogene Protein c-ets-1
  • Proto-Oncogene Proteins / biosynthesis
  • Proto-Oncogene Proteins / metabolism*
  • Proto-Oncogene Proteins c-ets
  • Sequence Homology, Nucleic Acid
  • Transcription Factors / metabolism*
  • Transcription, Genetic
  • Tumor Cells, Cultured

Substances

  • ETS1 protein, human
  • MAS1 protein, human
  • Nuclear Proteins
  • Proto-Oncogene Mas
  • Proto-Oncogene Protein c-ets-1
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-ets
  • Transcription Factors