The G-quadruplex ligand telomestatin inhibits POT1 binding to telomeric sequences in vitro and induces GFP-POT1 dissociation from telomeres in human cells.

نویسندگان

  • Dennis Gomez
  • Marie-Françoise O'Donohue
  • Thomas Wenner
  • Céline Douarre
  • Jérome Macadré
  • Pascale Koebel
  • Marie-Josèphe Giraud-Panis
  • Hervé Kaplan
  • Alain Kolkes
  • Kazuo Shin-ya
  • Jean-François Riou
چکیده

Telomestatin is a potent G-quadruplex ligand that specifically interacts with the 3' telomeric overhang, leading to its degradation and that induces a delayed senescence and apoptosis of cancer cells. Protection of Telomere 1 (POT1) was recently identified as a specific single-stranded telomere-binding protein involved in telomere capping and T-loop maintenance. We showed here that a telomestatin treatment inhibits POT1 binding to the telomeric overhang in vitro. The treatment of human EcR293 cells by telomestatin induces a dramatic and rapid delocalization of POT1 from its normal telomere sites but does not affect the telomere localization of the double-stranded telomere-binding protein TRF2. Thus, we propose that G-quadruplex stabilization at telomeric G-overhang inactivates POT1 telomeric function, generating a telomere dysfunction in which chromosome ends are no longer properly protected.

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عنوان ژورنال:
  • Cancer research

دوره 66 14  شماره 

صفحات  -

تاریخ انتشار 2006