Abstract
The highly oncogenic retrovirus reticuloendotheliosis virus (Rev) strain T (Rev-T) has, relative to its helper virus Rev strain A, a substitution of the oncogene v-rel for most of the env gene and a large deletion of gag and pol sequences. When the helper virus sequences that are deleted in Rev-T are replaced, the recombinant virus is nontransforming (I. S. Y. Chen and H. M. Temin, Cell 31: 111-120, 1982). We show that suppression of transformation occurs when several different DNA sequences are inserted in Rev-T and that suppression is correlated with a reduction in the amount of v-rel mRNA and v-rel protein in infected cells. The reduced amount of v-rel protein is insufficient for transformation.
MeSH Terms
Animals
Cell Transformation, Viral
Cells, Cultured
Chick Embryo
DNA, Viral/genetics
Defective Viruses/genetics
Gene Expression Regulation
Genes, Viral
Oncogene Proteins, Viral/genetics
Oncogenes
RNA Splicing
Reticuloendotheliosis virus/genetics
Retroviridae/genetics
Virus Replication
Chemicals
DNA, Viral
Oncogene Proteins, Viral
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Miller C K
Temin H M
References (23)
23 references, click to expand
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