The mammalian UV response: c-Jun induction is required for exit from p53-imposed growth arrest

Cell. 2000 Dec 8;103(6):897-907. doi: 10.1016/s0092-8674(00)00193-8.

Abstract

The mammalian UV response results in rapid and dramatic induction of c-jun. Induction of a protooncogene, normally involved in mitogenic responses, by a genotoxic agent that causes growth arrest seems paradoxical. We now provide an explanation for the role of c-Jun in the UV response of mouse fibroblasts. c-Jun is necessary for cell-cycle reentry of UV-irradiated cells, but does not participate in the response to ionizing radiation. Cells lacking c-Jun undergo prolonged cell-cycle arrest, but resist apoptosis, whereas cells that express c-Jun constitutively do not arrest and undergo apoptosis. This function of c-Jun is exerted through negative regulation of p53 association with the p21 promoter. Cells lacking c-Jun exhibit prolonged p21 induction, whereas constitutive c-Jun inhibits UV-mediated p21 induction.

Publication types

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

MeSH terms

  • Animals
  • Cell Cycle*
  • Cell Line
  • Cell Survival
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins / antagonists & inhibitors
  • Cyclins / genetics
  • Cyclins / metabolism*
  • DNA / biosynthesis
  • DNA / metabolism
  • Enzyme Inhibitors / metabolism
  • Fibroblasts
  • Gene Expression Regulation*
  • Genes, Reporter
  • Genes, jun / genetics*
  • Humans
  • Mice
  • Signal Transduction
  • Transcription, Genetic / genetics
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism*
  • Ultraviolet Rays*

Substances

  • CDKN1A protein, human
  • Cdkn1a protein, mouse
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins
  • Enzyme Inhibitors
  • Tumor Suppressor Protein p53
  • DNA