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MicroRNA-mediated gene silencing modulates the UV-induced DNA-damage response

  • Joris Pothof
  • , Nicole S. Verkaik
  • , Wilfred Van Ijcken
  • , Erik A.C. Wiemer
  • , Van T.B. Ta
  • , Gijsbertus T.J. Van Der Horst
  • , Nicolaas G.J. Jaspers
  • , Dik C. Van Gent
  • , Jan H.J. Hoeijmakers
  • , Stephan P. Persengiev

Research output: Contribution to journalArticlepeer-review

212 Citations (Scopus)

Abstract

DNA damage provokes DNA repair, cell-cycle regulation and apoptosis. This DNA-damage response encompasses gene-expression regulation at the transcriptional and post-translational levels. We show that cellular responses to UV-induced DNA damage are also regulated at the post-transcriptional level by microRNAs. Survival and checkpoint response after UV damage was severely reduced on microRNA-mediated gene-silencing inhibition by knocking down essential components of the microRNA-processing pathway (Dicer and Ago2). UV damage triggered a cell-cycle-dependent relocalization of Ago2 into stress granules and various microRNA-expression changes. Ago2 relocalization required CDK activity, but was independent of ATM/ATR checkpoint signalling, whereas UV-responsive microRNA expression was only partially ATM/ATR independent. Both microRNA-expression changes and stress-granule formation were most pronounced within the first hours after genotoxic stress, suggesting that microRNA-mediated gene regulation operates earlier than most transcriptional responses. The functionality of the microRNA response is illustrated by the UV-inducible miR-16 that downregulates checkpoint-gene CDC25a and regulates cell proliferation. We conclude that microRNA-mediated gene regulation adds a new dimension to the DNA-damage response.

Original languageEnglish
Pages (from-to)2090-2099
Number of pages10
JournalEMBO Journal
Volume28
Issue number14
DOIs
Publication statusPublished - 22 Jul 2009
Externally publishedYes

Keywords

  • Cell cycle checkpoints
  • DNA damage
  • MicroRNAs
  • Stress granules

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