Transactivation of the c-myc promoter by human T cell leukemia virus type 1 tax is mediated by NF kappa B

J Biol Chem. 1992 Aug 15;267(23):16288-91.

Abstract

Human T cell leukemia virus type 1 is the causative agent of adult T cell leukemia. The virus encodes a 40-kDa protein, tax, that is important for the immortalization of T cells. Expression of tax activates several cellular transcription factors, including NF kappa B. We have previously identified two functional NF kappa B binding sites within the murine c-myc gene: upstream regulatory element (URE) and internal regulatory element (IRE). Using transient cotransfection analysis of Jurkat or HeLa cells, we report that tax can transactivate chimeric TK-CAT constructs containing multiple copies of wild-type URE or IRE, but not constructs with mutated versions of these elements. Furthermore, tax induced transcriptional activity of murine and human c-myc promoter-CAT hybrid genes in Jurkat and HeLa cells. A mutated tax expression vector, which fails to activate NF kappa B, was unable to induce either murine or human c-myc-CAT or URE/IRE-TK-CAT constructs. Mutant c-myc gene-CAT constructs, in which the URE and IRE were mutated either singly or in combination by site directed mutagenesis, displayed significantly reduced CAT activation upon cotransfection with a tax expression vector. These results suggest that tax can transactivate the c-myc gene through NF kappa B. The tax-induced stimulation of this oncogene may play a role in T cell immortalization.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Base Sequence
  • Chloramphenicol O-Acetyltransferase / genetics
  • Chloramphenicol O-Acetyltransferase / metabolism
  • Genes, myc*
  • Genes, pX*
  • Genetic Vectors
  • HeLa Cells
  • Human T-lymphotropic virus 1 / genetics*
  • Human T-lymphotropic virus 1 / metabolism
  • Humans
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • NF-kappa B / genetics
  • NF-kappa B / metabolism*
  • Oligodeoxyribonucleotides
  • Promoter Regions, Genetic*
  • Recombinant Proteins / metabolism
  • Repetitive Sequences, Nucleic Acid
  • Restriction Mapping
  • Transcriptional Activation*
  • Transfection

Substances

  • NF-kappa B
  • Oligodeoxyribonucleotides
  • Recombinant Proteins
  • Chloramphenicol O-Acetyltransferase