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PMID: 6095071 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Expression of the Rous sarcoma virus src gene in avian macrophages fails to elicit transformed cell phenotype.

Molecular and cellular biology ·Vol. 4 ·No. 7 ·1984-07-00 ·Pages 1420-4

Lipsich L, Brugge JS, Boettiger D

Abstract

Infection of avian macrophages with Rous sarcoma virus does not induce any changes in the morphology, growth behavior, or expression of macrophage-specific proteins. The absence of cellular transformation does not result from a block in the synthesis of viral proteins, since infectious viruses are released from a majority of cells in the culture. In this report, we examine the synthesis, processing, and functional activity of pp60src in Rous sarcoma virus-infected macrophages to determine whether the absence of transformation is due to an alteration in the functional expression of pp60src. Although the absolute level of pp60src was reduced compared with fibroblasts, the protein exhibited the same phosphorylation pattern and subcellular distribution and was able to phosphorylate immunoglobulin in the immune complex-protein kinase assay. These results imply that the failure of Rous sarcoma virus to transform macrophage may be due to a restriction in the cellular response to a functional src protein, perhaps due to the absence of cellular products which are essential for mediating pp60src-induced transformation.

MeSH Terms
Animals Avian Sarcoma Viruses/genetics Cell Transformation, Viral Cells, Cultured Chick Embryo Genes Genes, Viral Macrophages/physiology Oncogene Protein pp60(v-src) Phenotype Protein Kinases/genetics Viral Proteins/genetics Yolk Sac
Chemicals
Viral Proteins Protein Kinases Oncogene Protein pp60(v-src)
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Lipsich L
Brugge J S
Boettiger D
References (37)
37 references, click to expand
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Article Info
Journal
Molecular and cellular biology
Abbr.
Mol Cell Biol
ISSN
0270-7306
Published
1984-07-00
Pages
1420-4
Language
English
Region
United States
NLM ID
8109087
PMCID
PMC368926
Subset
IM
Grants
NCI NIH HHS · CA2814604 · United States
NCI NIH HHS · CA30383 · United States
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