Data di Pubblicazione:
2021
Abstract:
Telomerase negative cancer cell types use the Alternative Lengthening of Telomeres (ALT) pathway to elongate telomeres ends. Here, we show that silencing human DNA polymerase (Pol lambda) in ALT cells represses ALT activity and induces telomeric stress. In addition, replication stress in the absence of Pol lambda, strongly affects the survival of ALT cells. In vitro, Pol lambda can promote annealing of even a single G-rich telomeric repeat to its complementary strand and use it to prime DNA synthesis. The noncoding telomeric repeat containing RNA TERRA and replication protein A negatively regulate this activity, while the Protection of Telomeres protein 1 (POT1)/TPP1 heterodimer stimulates Pol lambda. Pol lambda associates with telomeres and colocalizes with TPP1 in cells. In summary, our data suggest a role of Pol lambda in the maintenance of telomeres by the ALT mechanism.
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
DNA double-strand breaks (DSBs); extra-chromosomal telomeric repeats (ECTRs); promyelocytic leukemia (PML) bodies; alternative lengthening of telomeres (ALT); DNA polymerase lambda; microhomology-mediated strand transfer (MMST) activity; telomere dysfunction-induced foci (TIFs); telomere stress.
Elenco autori:
Maga, Giovanni; Crespan, Emmanuele; Sabbioneda, Simone; D'ADDA DI FAGAGNA, Fabrizio; Francia, Sofia; Garbelli, Anna
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