Independent recombination between avian leukosis virus terminal sequences and host DNA in virus-induced proliferative disease.
Open Access
- 1 March 1981
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 78 (3), 1896-1900
- https://doi.org/10.1073/pnas.78.3.1896
Abstract
A c(complementary)DNA transcript of Rous sarcoma virus, which contained the long terminal repeat (LTR) and some additional 3''-terminal sequences, was inserted into the plasmid pBR322. This recombinant plasmid, p53, was then used as a hybridization probe to detect viral terminal sequences in DNA from a number of tissues of birds chickens with a variety of avian leukosis virus (ALV)-induced proliferative diseases. Using restriction endonuclease digestion and blot hybridization analysis, standard ALV genomes and viral terminal sequences linked to host DNA and not to viral genes were detected. In DNA from bursal lymphomas and nephroblastomas, small numbers of integration sites occupied by sequences in p53 and lacking most or all of the remainder of the viral genome were observed. In DNA from osteopetrosis, apparently multiple copies of molecules containing host DNA linked to viral LTR sequences were observed. Some of these structures were contained in discrete, probably unintegrated DNA molecules. Viral LTR sequences can apparently be inserted as independent elements during recombination with host DNA in some forms of interaction between exogenous retroviruses and host cells. Because the LTR have been implicated in integration and transcription of viral genes, the possibility that translocation or activation, or both, of host genes may occur as a consequence of viral infection is reinforced by these observations.Keywords
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