ssDNA fragments induce cell senescence by telomere uncapping

Avgi Tsolou, João F. Passos, Glyn Nelson, Yasumichi Arai, Thomas von Zglinicki

Research output: Contribution to journalArticle

14 Scopus citations

Abstract

Telomere uncapping is known to induce senescence by activating a DNA damage response (DDR). However, it is still unclear what structural features of uncapped telomeres activate DDR. One hypothesis is that the exposure of the telomeric single-stranded G-rich 3′ overhang triggers a DNA damage response and is, thus, equivalent to telomere uncapping. To mimic this, we compared the effects of two short single-stranded oligonucleotides, (TTAGGG)2 and (CCCTAA)2. G-rich oligonucleotides induced DNA damage foci containing γH2AX and senescence-like arrest, whilst C-rich oligonucleotides had no effect. Oligonucleotides did not co-localize with γΗ2ΑX foci, instead the induced DNA damage foci were preferentially localized at telomeres. BrdU incorporation assays showed that the effect of G oligonucleotides on γH2AX foci formation was cell cycle-dependent; entry of cells into S phase was necessary for subsequent DNA damage foci formation. Together, our results show that short G-rich single-stranded oligonucleotides induce telomere uncapping in a cell cycle-dependent manner, probably by titrating essential factors like Pot1 away from telomeres.

Original languageEnglish (US)
Pages (from-to)892-899
Number of pages8
JournalExperimental Gerontology
Volume43
Issue number10
DOIs
StatePublished - Oct 1 2008

Keywords

  • DNA damage response
  • Oligonucleotides
  • Senescence
  • Telomere uncapping
  • Telomeres
  • ssDNA

ASJC Scopus subject areas

  • Biochemistry
  • Aging
  • Molecular Biology
  • Genetics
  • Endocrinology
  • Cell Biology

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