Isolation of human oncogene sequences (v-fes homolog) from a cosmid library

Science (New York, N.Y.)
|June 4, 1982
PubMed

Insights

Researchers identified human cellular sequences homologous to the feline sarcoma virus (FeSV) v-fes gene. These human sequences, when transfected into cells, did not show transforming activity, suggesting they are not oncogenic.

Area of Science:

  • Molecular Biology
  • Oncogenomics
  • Virology

Background:

  • Feline sarcoma virus (FeSV) contains transforming sequences (v-fes gene) common to Gardner (GA) and Snyder Theilen (ST) isolates.
  • Understanding the human homolog of viral oncogenes is crucial for cancer research.

Purpose of the Study:

  • To identify and characterize the human homolog(s) of the v-fes gene found in FeSV.
  • To determine if the human v-fes homolog possesses transforming activity.

Main Methods:

  • Construction of a human lung carcinoma DNA library in a cosmid vector system.
  • Isolation and characterization of cosmid clones containing GA/ST FeSV v-fes homologous sequences.
  • Analysis of sequence homology and colinearity, including identification of potential introns.
  • Transfection of isolated human c-fes sequences into RAT-2 cells using a thymidine kinase selection system.

Main Results:

  • Three cosmid clones were isolated, containing approximately 56 kilobases of contiguous human DNA with GA/ST FeSV v-fes homologous sequences.
  • The homologous sequences were distributed discontinuously over a 9.5-kilobase region, indicating the presence of at least three introns.
  • Transfection of the human c-fes sequence into RAT-2 cells demonstrated no detectable transforming activity.

Conclusions:

  • The human genome contains sequences homologous to the FeSV v-fes gene.
  • The identified human c-fes sequence lacks the transforming potential observed in the viral v-fes gene.
  • This suggests that the human homolog may function differently or require additional factors for oncogenic transformation.