Activation of collagenase IV gene expression and enzymatic activity by the Moloney murine leukemia virus long terminal repeat

Virology. 1997 Jan 20;227(2):331-42. doi: 10.1006/viro.1996.8345.

Abstract

Moloney murine leukemia virus (Mo-MuLV) is a thymotropic and leukemogenic retrovirus which causes T lymphomas and leukemias, yet does not contain a transforming gene product. Mo-MuLV has been shown to trans-activate cellular genes via a polymerase III-generated transcript, designated let, from the long terminal repeat (LTR). Here we demonstrate that introduction of the Mo-MuLV LTR stably, or transiently, into murine or human cultured cells resulted in an 8- to 15-fold increase in collagenase IV (92-kDa gelatinase, gelatinase B, matrix metalloproteinase-9) gene expression. Collagenase IV protein expression was induced 9-fold by stable integration of MuLV LTR, as measured by immunoblot analysis using an anti-collagenase IV polyclonal antibody. The MuLV LTR coordinately stimulated the proteolytic activity of collagenase IV by 14-fold. The AP-1-binding site in the collagenase IV promoter was required for transactivation by the LTR. Collagenase type IV degrades type IV collagen, a major component of basement membrane, which constitutes the first step of the metastatic cascade. The activation of proteolytic enzymes by the MuLV LTR may thus play a contributory role in the development or spread of virus-induced lymphomas or leukemias.

Publication types

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

MeSH terms

  • 3T3 Cells
  • Animals
  • Chloramphenicol O-Acetyltransferase / biosynthesis
  • Collagenases / biosynthesis*
  • Collagenases / genetics*
  • DNA Probes
  • Gene Expression Regulation, Enzymologic
  • Gene Expression Regulation, Viral*
  • Genes, Reporter
  • HeLa Cells
  • Humans
  • Matrix Metalloproteinase 9
  • Mice
  • Moloney murine leukemia virus / genetics*
  • Polymerase Chain Reaction
  • Promoter Regions, Genetic
  • Recombinant Fusion Proteins / biosynthesis
  • Repetitive Sequences, Nucleic Acid*
  • Transcription, Genetic
  • Transcriptional Activation*
  • Transfection

Substances

  • DNA Probes
  • Recombinant Fusion Proteins
  • Chloramphenicol O-Acetyltransferase
  • Collagenases
  • Matrix Metalloproteinase 9