-transparent.png){kind=logo}
The genome of the defective, murine spleen focus-forming Friend virus (SFFV) was identified as a 50S RNA complex consisting of 32S RNA monomers. Electrophoretic mobility and the molecular weights of unique RNase T1-resistant oligonucleotides (T1-oligonucleotides) indicated that the 32S RNA had a complexity of about 7.4 kilobases. Hybridization with DNA complementary to Friend murine leukemia virus (Fr-MLV) has distinguished two sets of nucleotide sequences in 32S SFFV RNA, 74% which were Fr-MLV related and 26% which were SFFV specific. By the same method, SFFV RNA was 48% related to Moloney MLV. We have resolved 23 large T1-oligonucleotides of SFFV RNA and 43 of Fr-MLV RNA. On the basis of the relationship between SFFV and Fr-MLV RNAs, the 23 SFFV oligonucleotides fell into four classes: (i) seven which had homologous equivalents in Fr-MLV RNA; (ii) six more which could be isolated from SFFV RNA-Fr-MLV cDNA hybrids treated with RNases A and T1; (iii) eight more which were isolated from hybrids treated with RNases A and T1; and (iv) two which did not have Fr-MLV-related counterparts. Surprisingly, the two class iv oligonucleotides had homologous counterparts in the RNA of six amphotropic MLV's including mink cell focus-forming and HIX-MLVs analyzed previously. The map locations of the 23 SFFV T1-oligonucleotides relative to the 3' polyadenylic acid coordinate of SFFV RNA were deduced from the size of the smallest polyadenylic acid-tagged RNA fragment from which a given oligonucleotide was isolated. The resulting oligonucleotide map could be divided roughly into three segments: two terminal segments which are mosaics of oligonucleotides of classes i, ii, and iii and an internal segment between 2 and 2.5 kilobases from the 3' end containing the two oligonucleotides shared with amphotropic MLVs. Since SFFV RNA consists predominantly of sequence elements related to ecotropic and amphotropic helper-independent MLVs, it would appear that the transforming gene of SFFV is not a major specific sequence unrelated to genes of helper viruses, as is the case with Rous sarcoma and probably withe other defective sarcoma and acute leukemia viruses.
L H Evans, and
P H Duesberg, and
D H Troxler, and
E M Scolnick
June 1981,
The Journal of general virology,
L H Evans, and
P H Duesberg, and
D H Troxler, and
E M Scolnick
February 1971,
Nature: New biology,
L H Evans, and
P H Duesberg, and
D H Troxler, and
E M Scolnick
November 1982,
The Journal of general virology,
L H Evans, and
P H Duesberg, and
D H Troxler, and
E M Scolnick
January 1980,
Cold Spring Harbor symposia on quantitative biology,
L H Evans, and
P H Duesberg, and
D H Troxler, and
E M Scolnick
June 1971,
Journal of the National Cancer Institute,
L H Evans, and
P H Duesberg, and
D H Troxler, and
E M Scolnick
October 1985,
Proceedings of the National Academy of Sciences of the United States of America,
L H Evans, and
P H Duesberg, and
D H Troxler, and
E M Scolnick
March 1976,
Journal of the National Cancer Institute,
L H Evans, and
P H Duesberg, and
D H Troxler, and
E M Scolnick
March 1985,
Virology,
L H Evans, and
P H Duesberg, and
D H Troxler, and
E M Scolnick
September 1978,
The Journal of experimental medicine,
L H Evans, and
P H Duesberg, and
D H Troxler, and
E M Scolnick
October 1977,
Journal of virology,
