Isolation of v-fms and its human cellular homolog

Virology. 1983 Apr 15;126(1):248-58. doi: 10.1016/0042-6822(83)90476-2.


The integrated form of McDonough FeSV proviral DNA, including cellular flanking sequences, was molecularly cloned from nonproductively transformed Fisher rat cells. Acquired cellular-derived (v-fms) sequences within the cloned proviral DNA were mapped from between 2.6 and 5.5 kb from the 5'LTR. Upon transfection, the cloned proviral DNA was biologically active; it caused induction of the transformed phenotype and the resulting transformed cells expressed the major McDonough FeSV translational product, P170gag-fms at high level. Using a series of molecular probes representing subgenomic regions of the viral v-fms gene, a cosmid library of human lung carcinoma DNA was screened for v-fms homologous sequences. Three cosmid clones containing overlapping v-fms homologous cellular DNA inserts, representing a contiguous region of cellular DNA sequence of approximately 64 kb in length, were isolated. Within this region of human genomic DNA, v-fms homologous sequences are dispersed over a total region of around 32 kb. These represent the entire human cellular homolog of v-fms, are colinear with the viral v-fms transforming gene, and contain a minimum of four intervening sequences. At least 12 regions of highly repetitive DNA sequences have been mapped in close proximity to c-fms coding sequences.

Publication types

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

MeSH terms

  • Animals
  • Base Sequence
  • Cell Line
  • Cell Transformation, Neoplastic
  • Cell Transformation, Viral
  • Cloning, Molecular*
  • DNA Restriction Enzymes
  • Genes, Viral*
  • Genetic Vectors
  • Humans
  • Lung Neoplasms / genetics
  • Nucleic Acid Hybridization
  • Oncogenes*
  • Rats
  • Recombination, Genetic
  • Retroviridae / genetics*
  • Sarcoma Viruses, Feline / genetics*


  • DNA Restriction Enzymes