Repression of c-fos transcription and an altered genetic program in senescent human fibroblasts

Science. 1990 Jan 12;247(4939):205-9. doi: 10.1126/science.2104680.

Abstract

Normal cells in culture invariably undergo senescence, whereby they cease proliferation after a finite number of doublings. Irreversible changes in gene expression occurred in senescent human fetal lung fibroblasts: a non-cell cycle-regulated mRNA was partially repressed; an unusual polyadenylated histone mRNA was expressed; although serum induced c-H-ras, c-myc, and ornithine decarboxylase mRNA normally, ornithine decarboxylase activity was deficient; and serum did not induce mRNA for a replication-dependent histone and for the c-fos proto-oncogene. The loss of c-fos inducibility was the result of a specific, transcriptional block. The results suggest that senescent fibroblasts were unable to proliferate because of, at least in part, selective repression of c-fos; moreover, the multiple changes in gene expression support the view that cellular senescence is a process of terminal differentiation.

Publication types

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

MeSH terms

  • Blood
  • Cell Division
  • Cell Line
  • Cell Survival / physiology
  • Embryo, Mammalian
  • Fibroblasts / cytology*
  • Fibroblasts / metabolism
  • Gene Expression / physiology*
  • Humans
  • Ornithine Decarboxylase / genetics
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins / genetics*
  • Proto-Oncogene Proteins c-fos
  • Proto-Oncogene Proteins c-myc
  • Proto-Oncogene Proteins p21(ras)
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Suppression, Genetic*
  • Transcription, Genetic*

Substances

  • MAS1 protein, human
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-fos
  • Proto-Oncogene Proteins c-myc
  • RNA, Messenger
  • HRAS protein, human
  • Proto-Oncogene Proteins p21(ras)
  • Ornithine Decarboxylase