NDLI: Independent recombination between avian leukosis virus terminal sequences and host DNA in virus-induced proliferative disease.

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Selective inhibition of Escherichia coli protein synthesis and growth by nonionic oligonucleotides complementary to the 3' end of 16S rRNA.

Site-specific cleavage by T1 RNase of U-1 RNA in u-1 ribonucleoprotein particles.

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Related 5S RNA transcription factors in Xenopus oocytes and somatic cells.

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Independent recombination between avian leukosis virus terminal sequences and host DNA in virus-induced proliferative disease.

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Independent recombination between avian leukosis virus terminal sequences and host DNA in virus-induced proliferative disease.

Content Provider	World Health Organization (WHO)-Global Index Medicus
Author	Beemon, K. Neiman, P. Luce, J. A.
Abstract	A cDNA 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 with a variety of avian leukosis virus (ALV)-induced proliferative diseases. Using restriction endonuclease digestion and blot hybridization analysis, we detected, in addition to standard ALV genomes, viral terminal sequences linked to host DNA and not to viral genes. In DNA from bursal lymphomas and nephroblastomas, we observed small numbers of integration sites occupied by sequences in p53 and lacking most or all of the remainder of the viral genome. In DNA from osteopetrosis, we observed apparently multiple copies of molecules containing host DNA linked to viral LTR sequences. Some of these structures were contained in discrete, probably unintegrated, DNA molecules. We concluded that viral LTR sequences can be inserted as independent elements during recombination with host DNA in some forms of interaction between exogenous retroviruses and host cells. Because the LTRs 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.
ISSN	00278424
e-ISSN	10916490
Journal	Proceedings of the National Academy of Sciences of the United States of America
Issue Number	3
Volume Number	78
Language	English
Publisher	National Academy of Sciences
Publisher Date	1981-07-01
Publisher Place	United States
Access Restriction	Open
Subject Keyword	Avian Leukosis Virus Genetics DNA, Neoplasm DNA, Recombinant Metabolism DNA, Viral Kidney Neoplasms Microbiology Lymphoma Recombination, Genetic Wilms Tumor Animals Avian Sarcoma Viruses DNA Restriction Enzymes Neoplasms, Experimental Nucleic Acid Hybridization Plasmids Repetitive Sequences, Nucleic Acid Research Support, U.S. Gov't, P.H.S. Multidisciplinary
Content Type	Text
Resource Type	Article
Subject	Multidisciplinary

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