SV40-mediated immortalization of human fibroblasts

Exp Gerontol. 1996 Jan-Apr;31(1-2):303-10. doi: 10.1016/0531-5565(95)00024-0.

Abstract

We have identified a multistep mechanism by which the DNA virus SV40 overcomes cellular senescence. Expression of SV40 T antigen is required for both transient extension of life span and unlimited life span or immortalization. These effects are mediated through inactivation of function of growth suppressors pRB and p53 via complex formation with T antigen. However, immortalization additionally requires inactivation of a novel growth suppressor gene, which has recently been identified to be on the distal portion of the long arm of chromosome 6, designated SEN6. We propose that SEN6 is responsible for cellular senescence in fibroblasts and other cells.

Publication types

  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Antigens, Polyomavirus Transforming / physiology
  • Cell Transformation, Viral*
  • Cellular Senescence
  • Fibroblasts
  • Genes, Tumor Suppressor
  • Humans
  • Simian virus 40 / genetics*
  • Tumor Suppressor Protein p53 / physiology

Substances

  • Antigens, Polyomavirus Transforming
  • Tumor Suppressor Protein p53