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A new gene that controls the type of leukemia induced by Friend murine leukemia virus
Abstract:
NB tropic Friend murine leukemia virus (F-MuLV) replicates equally well in BALB/c and C57BL mice inoculated as neonates but causes almost exclusively erythroblastosis in BALB/c mice and nonerythroid (lymphoid and myelogenous) leukemias in C57BL mice. The C57BL resistance to erythroblastosis appears to be controlled by a single dominant gene in first and second backcrosses to BALB/c. This resistance to erythroblastosis is distinct from other genes known to affect susceptibility to Friend virus including Fv-1, Fv-2, H-2, Rfv-3, Fv-4, and Rmcf. We suggest the name Fhe for the new gene controlling susceptibility to Friend helper virus erythroblastosis.
Insights
A newly identified gene, Fhe, controls resistance to erythroblastosis in mice. This finding differentiates from previously known Friend virus susceptibility genes, offering new insights into leukemia development.
Area of Science:
- Virology
- Immunology
- Genetics
Background:
- Friend murine leukemia virus (F-MuLV) causes distinct leukemias in different mouse strains.
- BALB/c mice develop erythroblastosis, while C57BL mice develop nonerythroid leukemias upon F-MuLV infection.
Purpose of the Study:
- To identify the genetic basis for differential susceptibility to F-MuLV-induced erythroblastosis in mice.
- To characterize a novel gene controlling resistance to erythroblastosis.
Main Methods:
- Neonatal inoculation of BALB/c and C57BL mice with F-MuLV.
- Genetic analysis using first and second backcrosses to BALB/c.
- Comparison with known Friend virus susceptibility genes (Fv-1, Fv-2, H-2, Rfv-3, Fv-4, Rmcf).
Main Results:
- F-MuLV replicated similarly in both mouse strains.
- C57BL mice exhibited resistance to erythroblastosis, a trait controlled by a single dominant gene.
- This resistance gene is distinct from previously identified Fv genes.
Conclusions:
- A novel gene, designated Fhe, controls resistance to Friend helper virus-induced erythroblastosis.
- The Fhe gene provides a new genetic locus for understanding Friend virus leukemogenesis.
- This discovery aids in dissecting the complex genetic control of viral oncogenesis.