Related Experiment Video
Updated: Sep 2, 2026

Microarray-based Identification of Individual HERV Loci Expression: Application to Biomarker Discovery in Prostate Cancer
Published on: November 2, 2013
Isolation of human oncogene sequences (v-fes homolog) from a cosmid library
Abstract:
To define the human homolog (or homologs) of transforming sequences (v-fes gene) common to Gardner (GA) and Snyder Theilen (ST) isolates of feline sarcoma virus (FeSV), a representative library of human lung carcinoma DNA in a cosmid vector system was constructed. Three cosmid clones were isolated containing GA/ST FeSV v-fes homologous cellular sequences, within 32- to 42-kilobase cellular inserts representing 56 kilobases of contiguous human cellular DNA. Sequences both homologous to, and colinear with, GA or ST FeSV v-fes are distributed discontinuously over a region of up to 9.5 kilobases and contain a minimum of three regions of nonhomology representing probable introns. A thymidine kinase selection system was used to show that, upon transfection to RAT-2 cells, the human c-fes sequence lacked detectable transforming activity.
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.

