» Articles » PMID: 28760773

Alternative Lengthening of Telomeres Mediated by Mitotic DNA Synthesis Engages Break-Induced Replication Processes

Overview
Journal Mol Cell Biol
Specialty Cell Biology
Date 2017 Aug 2
PMID 28760773
Citations 117
Authors
Affiliations
Soon will be listed here.
Abstract

Alternative lengthening of telomeres (ALT) is a telomerase-independent telomere maintenance mechanism that occurs in a subset of cancers. By analyzing telomerase-positive cells and their human TERC knockout-derived ALT human cell lines, we show that ALT cells harbor more fragile telomeres representing telomere replication problems. ALT-associated replication defects trigger mitotic DNA synthesis (MiDAS) at telomeres in a RAD52-dependent, but RAD51-independent, manner. Telomeric MiDAS is a conservative DNA synthesis process, potentially mediated by break-induced replication, similar to type II ALT survivors in Replication stresses induced by ectopic oncogenic expression of cyclin E, G-quadruplexes, or R-loop formation facilitate the ALT pathway and lead to telomere clustering, a hallmark of ALT cancers. The TIMELESS/TIPIN complex suppresses telomere clustering and telomeric MiDAS, whereas the SMC5/6 complex promotes them. In summary, ALT cells exhibit more telomere replication defects that result in persistent DNA damage responses at telomeres, leading to the engagement of telomeric MiDAS (spontaneous mitotic telomere synthesis) that is triggered by DNA replication stress, a potential driver of genomic duplications in cancer.

Citing Articles

Multiple functions of the ALT favorite helicase, BLM.

Chang S, Tan J, Bao R, Zhang Y, Tong J, Jia T Cell Biosci. 2025; 15(1):31.

PMID: 40025590 PMC: 11871798. DOI: 10.1186/s13578-025-01372-3.


- Transcriptional Cascade Suggests Activation Mechanism for -Dependent Alternative Lengthening of Telomeres During Malignant Transformation of Malignant Peripheral Nerve Sheath Tumors: Elongation of Telomeres and Poor Survival.

Lee J, Choi E, Kim H, Kim Y, Kim S Biomedicines. 2025; 13(2).

PMID: 40002695 PMC: 11853032. DOI: 10.3390/biomedicines13020281.


Identification of modulators of the ALT pathway through a native FISH-based optical screen.

Azeroglu B, Khurana S, Wang S, Tricola G, Sharma S, Jubelin C Cell Rep. 2024; 44(1):115114.

PMID: 39729394 PMC: 11844024. DOI: 10.1016/j.celrep.2024.115114.


Identification of Novel Modulators of the ALT Pathway Through a Native FISH-Based Optical Screen.

Azeroglu B, Khurana S, Wang S, Tricola G, Sharma S, Jubelin C bioRxiv. 2024; .

PMID: 39605432 PMC: 11601530. DOI: 10.1101/2024.11.15.623791.


RAD52 and ERCC6L/PICH have a compensatory relationship for genome stability in mitosis.

Osia B, Merkell A, Lopezcolorado F, Ping X, Stark J PLoS Genet. 2024; 20(11):e1011479.

PMID: 39561207 PMC: 11614213. DOI: 10.1371/journal.pgen.1011479.


References
1.
Cesare A, Kaul Z, Cohen S, Napier C, Pickett H, Neumann A . Spontaneous occurrence of telomeric DNA damage response in the absence of chromosome fusions. Nat Struct Mol Biol. 2009; 16(12):1244-51. DOI: 10.1038/nsmb.1725. View

2.
Hahn W, Dessain S, Brooks M, King J, Elenbaas B, Sabatini D . Enumeration of the simian virus 40 early region elements necessary for human cell transformation. Mol Cell Biol. 2002; 22(7):2111-23. PMC: 133688. DOI: 10.1128/MCB.22.7.2111-2123.2002. View

3.
Choi E, Park P, Lee H, Lee Y, Kang G, Lee J . BRCA2 fine-tunes the spindle assembly checkpoint through reinforcement of BubR1 acetylation. Dev Cell. 2012; 22(2):295-308. DOI: 10.1016/j.devcel.2012.01.009. View

4.
Cox K, Marechal A, Flynn R . SMARCAL1 Resolves Replication Stress at ALT Telomeres. Cell Rep. 2016; 14(5):1032-1040. PMC: 5051350. DOI: 10.1016/j.celrep.2016.01.011. View

5.
Wu N, Kong X, Ji Z, Zeng W, Potts P, Yokomori K . Scc1 sumoylation by Mms21 promotes sister chromatid recombination through counteracting Wapl. Genes Dev. 2012; 26(13):1473-85. PMC: 3403015. DOI: 10.1101/gad.193615.112. View