%0 Journal Article %A Mol, J. N. M. %A Ostertag, W. %A Bilello, J. %A Stoof, T. J. %T Rauscher Spleen Focus-forming Virus: Biological Properties and Relationship to Helper Viruses %D 1982 %J Journal of General Virology, %V 63 %N 1 %P 45-56 %@ 1465-2099 %R https://doi.org/10.1099/0022-1317-63-1-45 %K Friend virus %K spleen focus-forming virus %K Rauscher virus %K BPA independence %I Microbiology Society, %X SUMMARY A Rauscher virus (RV)-transformed erythroid cell line, RA-1, was shown to be a non-producer cell line. RA-1 cells express not only gp51–54 env-related glycoprotein, but also gp70, which is more closely related to gp51–54 coded by a recombinant env gene than to the MuLV gp70. RA-1 cells could be infected by Friend, Moloney and Gross viruses, but not by the homologous Rauscher murine leukaemia virus. Rescue of spleen focus-forming activity was obtained on infection of these cells with MuLV-F or MuLV-Mol, but not with MuLV-Gross. The RNA of the RV complex resembles closely that of Friend virus (FV). It contains a 32S, presumably defective, genome, which most likely is responsible for spleen focus formation, and a 35S helper virus genome. Oligonucleotide fingerprint data suggest that RV has evolved independently of FV. Erythroid early BFU-E cells of mice infected with RV of Friend helper virus-infected RA-1 cells were shown to require no addition of conditioned medium to form large erythroid colonies (BFU-E) in the presence of only small amounts of erythropoietin. %U https://www.microbiologyresearch.org/content/journal/jgv/10.1099/0022-1317-63-1-45