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Transforming potential of a human protooncogene (c-fps/fes) locus
Summary
A human protooncogene, c-fps/fes, can functionally replace a large part of a feline sarcoma virus gene. This recombinant gene transforms mouse cells, demonstrating the carboxyl portion
Area of Science:
- Molecular Biology
- Oncogenes
- Retroviral Research
Background:
- The protooncogene c-fps/fes is a single vertebrate gene.
- It is homologous to avian sarcoma virus fps and feline sarcoma virus fes transforming genes.
- The human c-fps/fes locus has been previously cloned and characterized.
Purpose of the Study:
- To investigate the functional complementation of retroviral transforming proteins using human c-fps/fes sequences.
- To determine if a portion of the human c-fps/fes protein can substitute for the feline sarcoma virus fes transforming protein.
Main Methods:
- Construction of a recombinant gene replacing over 80% of feline sarcoma virus fes sequences with 3' human c-fps/fes sequences.
- Transformation of NIH 3T3 mouse fibroblasts with the recombinant gene.
- Analysis of protein kinase activity and phosphotyrosine levels in transformed cells.
Main Results:
- The recombinant gene successfully transformed NIH 3T3 mouse fibroblasts.
- The transformed cells exhibited increased phosphotyrosine levels.
- The recombinant protein encoded by the gene possessed protein kinase activity.
Conclusions:
- A significant carboxyl portion of the human c-fps/fes protein product can functionally complement a retroviral transforming protein.
- This finding highlights the conserved functional domains within oncogenes across different species.
- The study provides insights into the mechanism of retroviral transformation and oncogene function.