| Přispěvatelé: |
Buemi, Valentina, Schillaci, Odessa, Santorsola, Mariangela, Bonazza, Deborah, Broccia, Pamela Veneziano, Zappone, Annie, Bottin, Cristina, Dell'Omo, Giulia, Kengne, Sylvie, Cacchione, Stefano, Raffa, Grazia Daniela, Piazza, Silvano, di Fagagna, Fabrizio d'Adda, Benetti, Roberta, Cortale, Maurizio, Zanconati, Fabrizio, Del Sal, Giannino, Schoeftner, Stefan |
| Popis: |
Pathways that direct the selection of the telomerase-dependent or recombination-based, alternative lengthening of telomere (ALT) maintenance pathway in cancer cells are poorly understood. Using human lung cancer cells and tumor organoids we show that formation of the 2,2,7-trimethylguanosine (TMG) cap structure at the human telomerase RNA 5′ end by the Trimethylguanosine Synthase 1 (TGS1) is central for recruiting telomerase to telomeres and engaging Cajal bodies in telomere maintenance. TGS1 depletion or inhibition by the natural nucleoside sinefungin impairs telomerase recruitment to telomeres leading to Exonuclease 1 mediated generation of telomere 3′ end protrusions that engage in RAD51-dependent, homology directed recombination and the activation of key features of the ALT pathway. This indicates a critical role for 2,2,7-TMG capping of the RNA component of human telomerase (hTR) in enforcing telomerase-dependent telomere maintenance to restrict the formation of telomeric substrates conductive to ALT. Our work introduces a targetable pathway of telomere maintenance that holds relevance for telomere-related diseases such as cancer and aging. |
