Literature DB >> 2823459

Biological properties of simian virus 40 host range mutants lacking the COOH-terminus of large T antigen.

C N Cole1, T P Stacy.   

Abstract

Three mutants of simian virus 40 (SV40), with deletions near the 3' end of the A gene, displayed a host range phenotype for growth and virus production in various African green monkey kidney cell lines. The mutants formed plaques in CV-1P cells at 40.5 degrees, in BSC-1 cells at 37 and 40.5 degrees, and in Vero cells at 32, 37, and 40.5 degrees. Virus yields in these three lines were cold sensitive: the burst size was greatest at 40.5 degrees and least at 32 degrees, but some progeny was produced under all conditions examined. Mutant yields never exceeded 10% of wild-type yields under the most permissive conditions (Vero cells at 37 or 40 degrees) and were less than 1% of wild type under the most restrictive conditions (CV-1P cells at 32 degrees). These mutants can be complemented by any SV40 mutant which produces a large T antigen containing a normal COOH-terminus. Mutants whose T antigens could not be transported to the nucleus were most efficient at complementation. Mutant virus production in a line of rhesus monkey kidney cells and in primary cultures of African green and rhesus monkey kidney cells was also substantially below wild type. These mutants were also completely defective for adenovirus helper function. Our data suggest that the host range property and adenovirus helper function represent the same activities of large T antigen.

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Year:  1987        PMID: 2823459     DOI: 10.1016/0042-6822(87)90183-8

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  14 in total

1.  Interaction of simian virus 40 large T-antigen with cellular DNA polymerase alpha: studies with various T-antigen mutants of SV40.

Authors:  J M Pistillo; J K Vishwanatha
Journal:  Arch Virol       Date:  1991       Impact factor: 2.574

2.  Mapping of helicase and helicase substrate-binding domains on simian virus 40 large T antigen.

Authors:  K Wun-Kim; D T Simmons
Journal:  J Virol       Date:  1990-05       Impact factor: 5.103

3.  Nucleotide sequence of the human polyomavirus AS virus, an antigenic variant of BK virus.

Authors:  J E Tavis; D L Walker; S D Gardner; R J Frisque
Journal:  J Virol       Date:  1989-02       Impact factor: 5.103

4.  Removal of a small C-terminal region of JCV and SV40 large T antigens has differential effects on transformation.

Authors:  Nicole T M Seneca; Maria Teresa Sáenz Robles; James M Pipas
Journal:  Virology       Date:  2014-08-16       Impact factor: 3.616

5.  Complete nucleotide sequence of polyomavirus SA12.

Authors:  Paul Cantalupo; Adrienne Doering; Christopher S Sullivan; Achintya Pal; K W C Peden; Andrew M Lewis; James M Pipas
Journal:  J Virol       Date:  2005-10       Impact factor: 5.103

6.  Simian virus 40 host range/helper function mutations cause multiple defects in viral late gene expression.

Authors:  T Stacy; M Chamberlain; C N Cole
Journal:  J Virol       Date:  1989-12       Impact factor: 5.103

7.  Linker insertion mutants of simian virus 40 large T antigen that show trans-dominant interference with wild-type large T antigen map to multiple sites within the T-antigen gene.

Authors:  J Y Zhu; C N Cole
Journal:  J Virol       Date:  1989-11       Impact factor: 5.103

Review 8.  Emergent human pathogen simian virus 40 and its role in cancer.

Authors:  Regis A Vilchez; Janet S Butel
Journal:  Clin Microbiol Rev       Date:  2004-07       Impact factor: 26.132

9.  Simian virus 40 large T antigen host range domain functions in virion assembly.

Authors:  S L Spence; J M Pipas
Journal:  J Virol       Date:  1994-07       Impact factor: 5.103

10.  A novel translational regulation function for the simian virus 40 large-T antigen gene.

Authors:  P Rajan; S Swaminathan; J Zhu; C N Cole; G Barber; M J Tevethia; B Thimmapaya
Journal:  J Virol       Date:  1995-02       Impact factor: 5.103

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