Literature DB >> 8392612

Primary rat cells expressing a hybrid polyomavirus-simian virus 40 large T antigen have altered growth properties.

J J Manfredi1, C Prives.   

Abstract

Expression of simian virus 40 (SV40) large T antigen efficiently immortalizes and transforms primary cells. We previously reported that a hybrid polyomavirus-SV40 large T antigen, PyT1-521-SVT336-708, binds to both p53 and pRb but does not transform an established rat cell line (J. J. Manfredi and C. Prives, J. Virol. 64:5250-5259, 1990). Here we show that this hybrid large T antigen is capable of immortalizing primary rat cells. Plasmids that express resistance to G418 sulfate and either SV40 large T antigen or PyT1-521-SVT336-708 were transfected into primary rat embryo fibroblasts, and cell lines were established. The cell lines that expressed PyT1-521-SVT336-708 were not fully transformed but did exhibit altered growth properties. Although these PyT1-521-SVT336-708-expressing lines did not form foci, they did grow in low serum and grew to a high saturation density; these cell lines also formed colonies in soft agar, but their colonies were much smaller than those seen with an SV40 large-T-antigen-expressing line. PyT1-521-SVT336-708 also demonstrated the ability to cooperate with activated Ha-ras to form foci on primary rat embryo fibroblasts. Surprisingly, two types of morphologies in such lines were observed: refractile and spindle shaped. Although there was no correlation between T-antigen level and morphology, all lines that displayed refractile morphology expressed high levels of p21ras. Since the p53 binding activity of PyT1-521-SVT336-708 appears to be intact, these results suggest that there are functions residing in the amino end of SV40 large T antigen which are necessary for full transformation that are missing from the amino end of polyomavirus large T antigen. Conversely, conferring the ability to bind to p53 on an amino-terminal fragment of polyomavirus large T antigen, although not enough to allow full transformation function, does increase its oncogenic activity in saturation density and soft agar growth assays.

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Year:  1993        PMID: 8392612      PMCID: PMC237861     

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  57 in total

1.  AGAR SUSPENSION CULTURE FOR THE SELECTIVE ASSAY OF CELLS TRANSFORMED BY POLYOMA VIRUS.

Authors:  I MACPHERSON; L MONTAGNIER
Journal:  Virology       Date:  1964-06       Impact factor: 3.616

2.  Functional consequences of the interactions of the p53 tumor suppressor protein and SV40 large tumor antigen.

Authors:  C Prives; J Bargonetti; P N Friedman; J J Manfredi; E H Wang
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1991

3.  Mutations in polyomavirus large T affecting immortalization of primary rat embryo fibroblasts.

Authors:  A Larose; L St-Onge; M Bastin
Journal:  Virology       Date:  1990-05       Impact factor: 3.616

4.  Cell lines established by a temperature-sensitive simian virus 40 large-T-antigen gene are growth restricted at the nonpermissive temperature.

Authors:  P S Jat; P A Sharp
Journal:  Mol Cell Biol       Date:  1989-04       Impact factor: 4.272

5.  The cellular 107K protein that binds to adenovirus E1A also associates with the large T antigens of SV40 and JC virus.

Authors:  N Dyson; K Buchkovich; P Whyte; E Harlow
Journal:  Cell       Date:  1989-07-28       Impact factor: 41.582

6.  Mutants with changes within or near a hydrophobic region of simian virus 40 large tumor antigen are defective for binding cellular protein p53.

Authors:  K W Peden; A Srinivasan; J M Farber; J M Pipas
Journal:  Virology       Date:  1989-01       Impact factor: 3.616

7.  Wild-type p53 can inhibit oncogene-mediated focus formation.

Authors:  D Eliyahu; D Michalovitz; S Eliyahu; O Pinhasi-Kimhi; M Oren
Journal:  Proc Natl Acad Sci U S A       Date:  1989-11       Impact factor: 11.205

8.  Large T antigens of many polyomaviruses are able to form complexes with the retinoblastoma protein.

Authors:  N Dyson; R Bernards; S H Friend; L R Gooding; J A Hassell; E O Major; J M Pipas; T Vandyke; E Harlow
Journal:  J Virol       Date:  1990-03       Impact factor: 5.103

9.  An N-terminal transformation-governing sequence of SV40 large T antigen contributes to the binding of both p110Rb and a second cellular protein, p120.

Authors:  M E Ewen; J W Ludlow; E Marsilio; J A DeCaprio; R C Millikan; S H Cheng; E Paucha; D M Livingston
Journal:  Cell       Date:  1989-07-28       Impact factor: 41.582

10.  Ras-mediated cell cycle arrest is altered by nuclear oncogenes to induce Schwann cell transformation.

Authors:  A J Ridley; H F Paterson; M Noble; H Land
Journal:  EMBO J       Date:  1988-06       Impact factor: 11.598

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  3 in total

1.  Tiny T antigen: an autonomous polyomavirus T antigen amino-terminal domain.

Authors:  M I Riley; W Yoo; N Y Mda; W R Folk
Journal:  J Virol       Date:  1997-08       Impact factor: 5.103

2.  Stem Cell Secretome and Its Effect on Cellular Mechanisms Relevant to Wound Healing.

Authors:  Se-Ra Park; Jae-Wan Kim; Hee-Sook Jun; Joo Young Roh; Hwa-Yong Lee; In-Sun Hong
Journal:  Mol Ther       Date:  2017-10-05       Impact factor: 11.454

3.  Functional implications of mutations within polyomavirus large T antigen Rb-binding domain: effects on pRb and p107 binding in vitro and immortalization activity in vivo.

Authors:  A A Pilon; P Desjardins; J A Hassell; A M Mes-Masson
Journal:  J Virol       Date:  1996-07       Impact factor: 5.103

  3 in total

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