1. Alternative paths to telomere elongation.
- Author
-
Lee, Jennifer J., Lee, Junyeop, and Lee, Hyunsook
- Subjects
- *
TELOMERES , *CELLULAR aging , *PHASE separation , *TELOMERASE , *CANCER cells - Abstract
Overcoming cellular senescence that is induced by telomere shortening is critical in tumorigenesis. A majority of cancers achieve telomere maintenance through telomerase expression. However, a subset of cancers takes an alternate route for elongating telomeres: recombination-based alternative lengthening of telomeres (ALT). Current evidence suggests that break-induced replication (BIR), independent of RAD51, underlies ALT telomere synthesis. However, RAD51-dependent homologous recombination is required for homology search and inter-chromosomal telomere recombination in human ALT cancer cell maintenance. Accumulating evidence suggests that the breakdown of stalled replication forks, the replication stress, induces BIR at telomeres. Nevertheless, ALT research is still in its early stage and a comprehensive view is still unclear. Here, we review the current findings regarding the genesis of ALT, how this recombinant pathway is chosen, the epigenetic regulation of telomeres in ALT, and perspectives for clinical applications with the hope that this overview will generate new questions. [Display omitted] • Alternative lengthening of telomeres involves multiple recombination pathways. • Break-induced replication is the central mechanism underlying ALT TMM. • Replication stress caused by G-quadruplex or R-loop triggers telomere recombination. • Epigenetic control is crucial for ALT activity. • ALT telomeres cluster and display properties of liquid-liquid phase separation. [ABSTRACT FROM AUTHOR]
- Published
- 2021
- Full Text
- View/download PDF