Interaction of activated Ras with Raf-1 alone may be sufficient for transformation of rat2 cells

Mol Cell Biol. 1997 Jun;17(6):3047-55. doi: 10.1128/MCB.17.6.3047.

Abstract

v-H-ras effector mutants have been assessed for transforming activity and for the ability of the encoded proteins to interact with Raf-1-, B-Raf-, byr2-, ralGDS-, and CDC25-encoded proteins in the yeast two-hybrid system. Transformation was assessed in rat2 cells as well as in a mutant cell line, rv68BUR, that affords a more sensitive transformation assay. Selected mutant Ras proteins were also examined for their ability to interact with an amino-terminal fragment of Raf-1 in vitro. Finally, possible cooperation between different v-H-ras effector mutants and between effector mutants and overexpressed Raf-1 was assessed. Ras transforming activity was shown to correlate best with the ability of the encoded protein to interact with Raf-1. No evidence for cooperation between v-H-ras effector mutants was found. Signaling through the Raf1-MEK-mitogen-activated protein kinase cascade may be the only effector pathway contributing to RAS transformation in these cells.

MeSH terms

  • Animals
  • Binding Sites
  • Cell Cycle Proteins / metabolism
  • Cell Line
  • Cell Transformation, Neoplastic / genetics*
  • GTP-Binding Proteins / metabolism
  • Genes, Tumor Suppressor
  • Genes, ras / genetics*
  • In Vitro Techniques
  • Mutation
  • Phosphoprotein Phosphatases / metabolism
  • Protein Serine-Threonine Kinases / metabolism*
  • Proto-Oncogene Proteins / metabolism*
  • Proto-Oncogene Proteins c-raf
  • Rats
  • Signal Transduction / genetics
  • Transcription Factors / metabolism
  • ral Guanine Nucleotide Exchange Factor
  • rap GTP-Binding Proteins
  • ras Proteins / metabolism*
  • ras-GRF1

Substances

  • Cell Cycle Proteins
  • Proto-Oncogene Proteins
  • Transcription Factors
  • ral Guanine Nucleotide Exchange Factor
  • ras-GRF1
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-raf
  • Phosphoprotein Phosphatases
  • GTP-Binding Proteins
  • rap GTP-Binding Proteins
  • ras Proteins