Literature DB >> 227604

Characterization of different tumor antigens present in cells transformed by simian virus 40.

A E Smith, R Smith, E Paucha.   

Abstract

In addition to large T and small t antigens, cells transformed by simian virus 40 (SV40) commonly contain other proteins which specifically immunoprecipitate with SV40 anti-T serum and which are not detected in untransformed cells. The additional tumor antigens (T-Ags) fall into two groups: those having a close structural relationship with normal SV40 T-Ags, and those unrelated to large T and small t. The latter are probably nonviral T-Ags (NVT-Ags). The NVT-Ags comprise a family of proteins of molecular weight 50,000-55,000. Fingerprint analysis shows that NVT-Ags have few if any peptides in common with large T or small t, and that they lack the amino terminal tryptic peptide and the peptides unique to small t. NVT-Ags from different species have different fingerprints, but those isolated from different transformants of the same cell line are identical. The size of NVT is unaltered in cells transformed by mutants of SV40 with deletions in the region 0.60-0.55 map units. The mRNA for NVT does not hybridize to SV40 DNA. The other forms of T-Ag isolated from transformed cells fall into three classes: shortened forms of large T (truncated large T); multiple species of T-Ag with molecular weights very similar to, but distinct from, those of normal large T (large T doublets and triplets); and elongated forms of large T (super T). These proteins all contain the normal amino terminus of SV40 T-Ags, and the truncated forms of large T lack peptides from the carboxy terminal half of large T. One species of super T (molecular weight 130,000) contains only those methionine tryptic peptides present in normal large T, although it may contain some peptides in more than one copy.

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Year:  1979        PMID: 227604     DOI: 10.1016/0092-8674(79)90053-9

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  60 in total

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Journal:  RNA Biol       Date:  2013-10-14       Impact factor: 4.652

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3.  Abelson murine leukemia virus-transformed cells that lack p53 protein synthesis express aberrant p53 mRNA species.

Authors:  D Wolf; S Admon; M Oren; V Rotter
Journal:  Mol Cell Biol       Date:  1984-03       Impact factor: 4.272

4.  Wild-type and mutant p53 mediate cisplatin resistance through interaction and inhibition of active caspase-9.

Authors:  Jacqueline L Y Chee; Suzan Saidin; David P Lane; Sai Mun Leong; Jacqueline E Noll; Paul M Neilsen; Yi Ting Phua; Hani Gabra; Tit Meng Lim
Journal:  Cell Cycle       Date:  2012-01-15       Impact factor: 4.534

Review 5.  The first 30 years of p53: growing ever more complex.

Authors:  Arnold J Levine; Moshe Oren
Journal:  Nat Rev Cancer       Date:  2009-10       Impact factor: 60.716

6.  An oligomeric form of simian virus 40 large T-antigen is immunologically related to the cellular tumor antigen p53.

Authors:  K N Leppard; L V Crawford
Journal:  J Virol       Date:  1984-05       Impact factor: 5.103

7.  Immunoprecipitation of some forms of simian virus 40 large-T antigen by antibodies to synthetic peptides.

Authors:  E Paucha; R Harvey; A E Smith
Journal:  J Virol       Date:  1984-09       Impact factor: 5.103

8.  Structure and biochemical functions of four simian virus 40 truncated large-T antigens.

Authors:  F Chaudry; R Harvey; A E Smith
Journal:  J Virol       Date:  1982-10       Impact factor: 5.103

9.  Characterization of tau antigens isolated from uninfected and simian virus 40-infected monkey cells and papovavirus-transformed cells.

Authors:  D T Simmons
Journal:  J Virol       Date:  1980-11       Impact factor: 5.103

10.  Complex of simian virus 40 large-T antigen and host 53,000-molecular-weight protein in monkey cells.

Authors:  E Harlow; D C Pim; L V Crawford
Journal:  J Virol       Date:  1981-02       Impact factor: 5.103

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