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PMID: 6300663 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Stabilization of the 53,000-dalton nonviral tumor antigen is not required for transformation by simian virus 40.

Molecular and cellular biology ·Vol. 3 ·No. 2 ·1983-02-00 ·Pages 290-6

Sompayrac LM, Gurney EG, Danna KJ

Abstract

We have isolated a simian virus 40 deletion mutant, F8dl, that lacks the sequences from 0.168 to 0.424 map units. The deleted sequences represent about one-half of the coding region for large T antigen. We present evidence here that F8dl is able to transform mouse cells in a focus assay and that cell lines derived from these foci exhibit fully transformed phenotypes, have integrated mutant genomes, and express mutant-encoded proteins. This result implies that the region of the simian virus 40 genome between 0.168 and 0.424 map units is not essential for the maintenance of transformation. In addition, we have found that cells fully transformed by F8dl produce a 53,000-dalton nonviral tumor antigen (p53) that is as unstable as the p53 of untransformed cells. From this result we infer that transformation by simian virus 40 does not require the stabilization of p53.

MeSH Terms
Animals Antigens, Neoplasm/genetics Cell Transformation, Viral Cells, Cultured Haplorhini Molecular Weight Simian virus 40/genetics
Chemicals
Antigens, Neoplasm
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Sompayrac L M
Gurney E G
Danna K J
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32 references, click to expand
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Article Info
Journal
Molecular and cellular biology
Abbr.
Mol Cell Biol
ISSN
0270-7306
Published
1983-02-00
Pages
290-6
Language
English
Region
United States
NLM ID
8109087
PMCID
PMC368533
Subset
IM
Grants
NCI NIH HHS · CA-21797 · United States
NCI NIH HHS · CA-24924 · United States
NCRR NIH HHS · RR07013-16 · United States
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