p53 activity is selectively licensed in the Drosophila stem cell compartment

Elife. 2014 Mar 11:3:e01530. doi: 10.7554/eLife.01530.

Abstract

Oncogenic stress provokes tumor suppression by p53 but the extent to which this regulatory axis is conserved remains unknown. Using a biosensor to visualize p53 action, we find that Drosophila p53 is selectively active in gonadal stem cells after exposure to stressors that destabilize the genome. Similar p53 activity occurred in hyperplastic growths that were triggered either by the Ras(V12) oncoprotein or by failed differentiation programs. In a model of transient sterility, p53 was required for the recovery of fertility after stress, and entry into the cell cycle was delayed in p53(-) stem cells. Together, these observations establish that the stem cell compartment of the Drosophila germline is selectively licensed for stress-induced activation of the p53 regulatory network. Furthermore, the findings uncover ancestral links between p53 and aberrant proliferation that are independent of DNA breaks and predate evolution of the ARF/Mdm2 axis. DOI: http://dx.doi.org/10.7554/eLife.01530.001.

Keywords: Drosophila; biosensor; germline; oncogenic stress; p53; stem cells.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biosensing Techniques
  • Cell Cycle Checkpoints
  • Cell Proliferation
  • DNA Damage
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism*
  • Drosophila melanogaster / genetics
  • Drosophila melanogaster / metabolism*
  • Female
  • Fertility
  • Gene Expression Regulation
  • Genomic Instability
  • Infertility / genetics
  • Infertility / metabolism
  • Infertility / physiopathology
  • Ovary / metabolism*
  • Ovary / pathology
  • Ovary / physiopathology
  • Signal Transduction
  • Stem Cell Niche*
  • Stem Cells / metabolism*
  • Stem Cells / pathology
  • Stress, Physiological
  • Time Factors
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism*

Substances

  • Drosophila Proteins
  • Tumor Suppressor Protein p53
  • p53 protein, Drosophila