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PMID: 3005612 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Transforming Sloan-Kettering viruses generated from the cloned v-ski oncogene by in vitro and in vivo recombinations.

Journal of virology ·Vol. 57 ·No. 3 ·1986-03-00 ·Pages 1073-83

Stavnezer E, Barkas AE, Brennan LA, Brodeur D, Li Y

Abstract

The Sloan-Kettering viruses (SKVs) are replication-defective retroviruses that transform avian cells in vitro. Each of the three SKV isolates is a mixture of viruses with genomes ranging in size from 4.1 to 8.9 kilobases (kb) with a predominant genome of 5.7 kb. Using a cDNA representing a sequence, v-ski, that is SKV specific and held in common by the multiple SKV genomes, we generated a restriction map of the 5.7-kb SKV genome and molecularly cloned a ski-containing fragment from SKV proviral DNA. Southern hybridization and sequence analysis showed that the cloned DNA fragment consisted of the 1.3-kb ski sequence embedded in the p19gag sequence and followed by the remaining 5' half of the gag gene and small portions of both the pol and env genes. A large deletion encompassing the 3' half of gag and the 5' 80% of pol was mapped to a position about 1 kb downstream from the 3' ski-gag junction. To determine whether the cloned ski sequence had transforming activity, the ski-containing fragment and a cloned Rous-associated virus 1 (RAV-1) genome were used to construct an analog of the 5.7-kb SKV genome, RAV-SKV. Cotransfection of chicken embryo cells with RAV-SKV and RAV-1 yielded foci of transformed cells whose morphology was identical to that induced by the natural SKVs. The transformed transfected cells produced transforming virus with a 5.7-kb ski-containing genome and synthesized a gag-containing polyprotein of 110 kilodaltons (kDa). Several nonproducer clones of RAV-SKV-transformed cells were analyzed, and most were found to synthesize a 5.7-kb SKV RNA and a 110-kDa polyprotein. One clone was found to contain an 8.9-kb SKV RNA, and this clone synthesized a 125-kDa polyprotein. Since both the 5.7- and 8.9-kb genomes and the 110- and 125-kDa polyproteins had been identified in studies on the natural SKVs, the present results not only demonstrate the transforming activity of these individual SKVs but also suggest mechanisms for their generation.

MeSH Terms
Animals Avian Leukosis Virus/genetics Base Sequence Chick Embryo Cloning, Molecular DNA, Viral/analysis Gene Products, gag Genes, Viral Oncogene Proteins, Viral/analysis Oncogenes RNA, Viral/analysis Recombination, Genetic Retroviridae/genetics Retroviridae Proteins/genetics Transfection
Chemicals
DNA, Viral Gene Products, gag Oncogene Proteins, Viral RNA, Viral Retroviridae Proteins
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Stavnezer E
Barkas A E
Brennan L A
Brodeur D
Li Y
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Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1986-03-00
Pages
1073-83
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC252841
Subset
IM
Grants
NCI NIH HHS · CA 08748 · United States
NCI NIH HHS · CA 32817 · United States
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