TRF2-Mediated Control of Telomere DNA Topology as a Mechanism for Chromosome-End Protection.

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Benarroch-Popivker, Delphine | Pisano, Sabrina | Mendez-Bermudez, Aaron | Lototska, Liudmyla | Kaur, Parminder | Bauwens, Serge | Djerbi, Nadir | Latrick, Chrysa M | Fraisier, Vincent | Pei, Bei | Gay, Alexandre | Jaune, Emilie | Foucher, Kevin | Cherfils-Vicini, Julien | Aeby, Eric | Miron, Simona | Londoño-Vallejo, Arturo | Ye, Jing | Le Du, Marie-Hélène | Wang, Hong | Gilson, Eric | Giraud-Panis, Marie-Josèphe

Edité par CCSD ; Cell Press -

International audience. The shelterin proteins protect telomeres against activation of the DNA damage checkpoints and recombinational repair. We show here that a dimer of the shelterin subunit TRF2 wraps ∼ 90 bp of DNA through several lysine and arginine residues localized around its homodimerization domain. The expression of a wrapping-deficient TRF2 mutant, named Top-less, alters telomeric DNA topology, decreases the number of terminal loops (t-loops), and triggers the ATM checkpoint, while still protecting telomeres against non-homologous end joining (NHEJ). In Top-less cells, the protection against NHEJ is alleviated if the expression of the TRF2-interacting protein RAP1 is reduced. We conclude that a distinctive topological state of telomeric DNA, controlled by the TRF2-dependent DNA wrapping and linked to t-loop formation, inhibits both ATM activation and NHEJ. The presence of RAP1 at telomeres appears as a backup mechanism to prevent NHEJ when topology-mediated telomere protection is impaired.

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