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Experiments with cloned complete tumor-derived bovine leukemia virus information prove that the virus is totally exogenous to its target animal species
Author(s) -
Jacqueline Deschamps,
R. Kettmann,
Arsène Burny
Publication year - 1981
Publication title -
journal of virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.617
H-Index - 292
eISSN - 1070-6321
pISSN - 0022-538X
DOI - 10.1128/jvi.40.2.605-609.1981
Subject(s) - bovine leukemia virus , provirus , biology , virology , long terminal repeat , virus , vector (molecular biology) , genome , feline leukemia virus , murine leukemia virus , microbiology and biotechnology , leukemia , dna , restriction enzyme , endogenous retrovirus , genetics , recombinant dna , gene
Taking advantage of the existence of a unique SacI restriction site in the long terminal repeats of the integrated bovine leukemia virus proviral DNA isolated from a bovine tumor, the total viral information (about 9.2 kilobases) was cloned in the lambdoid vector lambda WES. lambda B. Use of this cloned bovine leukemia virus DNA allowed us, for the first time, to definitely rule out the existence of any endogenous bovine leukemia virus sequence in the bovine, ovine, caprine, murine, feline, chicken, or human genomes. These data prove the absence of acquired cellular information in the provirus that has given rise to a tumor.

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