» Articles » PMID: 194053

Properties of Permissive Monkey Cells Transformed by UV-irradiated Simian Virus 40

Overview
Journal J Virol
Date 1977 May 1
PMID 194053
Citations 36
Authors
Affiliations
Soon will be listed here.
Abstract

African green monkey cells (CV1 line) were infected with UV-irradiated simian virus 40 (SV40), and permissive lines of stably transformed cells were established. These cell lines display the SV40 T-antigen and the growth characteristics typical of nonpermissive transformed cells (e.g., reduced cell density inhibition, reduced serum dependence, ability to overgrow normal cells, and colony formation in soft agar). The level of permissiveness to superinfecting SV40 is fully comparable with that of nontransformed CV1 and BSC-1 lines. The transformed monkey lines also support SV40 plaque production under agar. By Cot analysis, the transformed permissive cells contain, on an average, 1 to 2 SV40 genome equivalents, and the majority of the viral sequences are associated with the high-molecular-weight cellular DNA. No spontaneous production of infectious SV40 has been observed. The transformed permissive monkey cells failed to support the replication of SV40 tsA mutants at the restrictive temperature. To account for this, it is suggested that the gene A product has separate functions for transformation and initiation of viral DNA synthesis, and only the former function is expressed in the transformed permissive monkey cells.

Citing Articles

Simian virus 40 (SV40) T-antigen mutations in tumorigenic transformation of SV40-immortalized human uroepithelial cells.

Kao C, Hauser P, Reznikoff W, Reznikoff C J Virol. 1993; 67(4):1987-95.

PMID: 8383222 PMC: 240267. DOI: 10.1128/JVI.67.4.1987-1995.1993.


Sequence-specific binding of simian virus 40 A protein to nonorigin and cellular DNA.

Wright P, DeLucia A, Tegtmeyer P Mol Cell Biol. 1984; 4(12):2631-8.

PMID: 6570189 PMC: 369271. DOI: 10.1128/mcb.4.12.2631-2638.1984.


Simian virus 40 large T-antigen point mutants that are defective in viral DNA replication but competent in oncogenic transformation.

Manos M, Gluzman Y Mol Cell Biol. 1984; 4(6):1125-33.

PMID: 6330530 PMC: 368881. DOI: 10.1128/mcb.4.6.1125-1133.1984.


DNA-binding properties of simian virus 40 T-antigen mutants defective in viral DNA replication.

Prives C, Covey L, Scheller A, Gluzman Y Mol Cell Biol. 1983; 3(11):1958-66.

PMID: 6318076 PMC: 370063. DOI: 10.1128/mcb.3.11.1958-1966.1983.


A functional simian virus 40 origin of replication is required for the generation of a super T antigen with a molecular weight of 100,000 in transformed mouse cells.

Chen S, Grass D, Blanck G, Hoganson N, Manley J, Pollack R J Virol. 1983; 48(2):492-502.

PMID: 6312105 PMC: 255374. DOI: 10.1128/JVI.48.2.492-502.1983.


References
1.
Maniatis T, Jeffrey A, Kleid D . Nucleotide sequence of the rightward operator of phage lambda. Proc Natl Acad Sci U S A. 1975; 72(3):1184-8. PMC: 432491. DOI: 10.1073/pnas.72.3.1184. View

2.
Burton K . A study of the conditions and mechanism of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acid. Biochem J. 1956; 62(2):315-23. PMC: 1215910. DOI: 10.1042/bj0620315. View

3.
Fogel M, Sachs L . Studies on the antigenic composition of hamster tumors induced by polyoma virus, and of normal hamster tissues in vivo and in vitro. J Natl Cancer Inst. 1962; 29:239-52. View

4.
Winocour E . Purification of polyoma virus. Virology. 1963; 19:158-68. DOI: 10.1016/0042-6822(63)90005-9. View

5.
Winocour E, Sachs L . Challenge infection of polyoma parotid tumor cells. Virology. 1962; 16:496-8. DOI: 10.1016/0042-6822(62)90231-3. View