Literature DB >> 2842713

Early gene expression and cellular DNA synthesis after stimulation of quiescent NIH3T3 cells with serum or purified simian virus 40.

M Mörike1, A Quaiser, D Müller, M Montenarh.   

Abstract

Like growth factors or hormones, the DNA tumor virus simian virus 40 can stimulate quiescent cells to re-enter the S-phase. Time course experiments revealed similar kinetics for the stimulation of cellular DNA synthesis by growth factors or SV40 infection, although there was a delay in DNA synthesis of about 2 h in the case of the SV40 infection. The analysis of the transcriptional activation of proto-oncogenes in cells stimulated by serum or SV40 infection revealed an enhanced transcription of a common set of proto-oncogenes, including c-myc and c-fos. Early on after infection of quiescent cells SV40 induced in addition the transcription of the c-sis gene which did not occur with UV-irradiated SV40 virus. Furthermore, we could demonstrate the presence of growth stimulating activities in medium from SV40 infected quiescent cells, which triggered quiescent cells to re-enter the cell cycle. These data suggest that SV40 might stimulate quiescent cells by inducing the transcription and ultimately the release of growth-factors.

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Year:  1988        PMID: 2842713

Source DB:  PubMed          Journal:  Oncogene        ISSN: 0950-9232            Impact factor:   9.867


  4 in total

1.  Tissue Tropism of SV40 Transformation of Human Cells: Role of the Viral Regulatory Region and of Cellular Oncogenes.

Authors:  Lei Zhang; Fang Qi; Giovanni Gaudino; Oriana Strianese; Haining Yang; Paul Morris; Harvey I Pass; Vivek R Nerurkar; Maurizio Bocchetta; Michele Carbone
Journal:  Genes Cancer       Date:  2010-10

2.  Transrepression of RNA polymerase II promoters by the simian virus 40 small t antigen.

Authors:  W B Wang; I Bikel; E Marsilio; D Newsome; D M Livingston
Journal:  J Virol       Date:  1994-10       Impact factor: 5.103

3.  Activation of the cellular transcription factor AP-1 in herpes simplex virus infected cells is dependent on the viral immediate-early protein ICPO.

Authors:  K L Jang; B Pulverer; J R Woodgett; D S Latchman
Journal:  Nucleic Acids Res       Date:  1991-09-25       Impact factor: 16.971

4.  Activation of c-Jun N-terminal kinase (JNK) pathway by HSV-1 immediate early protein ICP0.

Authors:  Lirong Diao; Bianhong Zhang; Chenghao Xuan; Shaogang Sun; Kai Yang; Yujie Tang; Wentao Qiao; Qimin Chen; Yunqi Geng; Chen Wang
Journal:  Exp Cell Res       Date:  2005-08-01       Impact factor: 3.905

  4 in total

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