The G-quadruplex Ligand Telomestatin Inhibits POT1 Binding to Telomeric Sequences In vitro and Induces GFP-POT1 Dissociation from Telomeres in Human Cells

D Gomez, MF O'Donohue, T Wenner, C Douarre… - Cancer research, 2006 - AACR
D Gomez, MF O'Donohue, T Wenner, C Douarre, J Macadré, P Koebel, MJ Giraud-Panis…
Cancer research, 2006AACR
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 …
Abstract
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. (Cancer Res 2006; 66(14): 6908-12)
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