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The nature of telomere fusion and a definition of the critical telomere length in human cells
Open accessAbstract
The loss of telomere function can result in telomeric fusion events that lead to the types of genomic rearrangements, such as nonreciprocal translocations, that typify early-stage carcinogenesis. By using single-molecule approaches to characterize fusion events, we provide a functional definition of fusogenic telomeres in human cells. We show that approximately half of the fusion events contained no canonical telomere repeats at the fusion point; of those that did, the longest was 12.8 repeats. Furthermore, in addition to end-replication losses, human telomeres are subjected to large-scale deletion events that occur in the presence or absence of telomerase. Here we show that these telomeres are fusogenic, and thus despite the majority of telomeres being maintained at a stable length in normal human cells, a subset of stochastically shortened telomeres can potentially cause chromosomal instability. Telomere fusion was accompanied by the deletion of one or both telomeres extending several kilobases into the telomere-adjacent DNA, and microhomology was observed at the fusion points. This contrasted with telomere fusion that was observed following the experimental disruption of TRF2. The distinct error-prone mutational profile of fusion between critically shortened telomeres in human cells was reminiscent of Ku-independent microhomology-mediated end-joining.
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“The segmental aneuploidies identified by cytogenetics analysis (Figs. 1B and S3-S5) most probably point to the occurrence of complex genomic rearrangements in OCT4-targeted samples, such as chromosomal translocations or end-to-end fusions, as it seems unlikely that the rest of the chromosome would continue to be retained without a telomere (31)(32)(33).”
From Frequent loss of heterozygosity in CRISPR-Cas9–edited early human embryos (2021) · cites this paper as [33]
In the citing paper
“Telomere fusions formed during telomere crisis in cultured cells are mediated by alt-NHEJ and exhibit insertion of new sequences at the fusion point75,76.”
From Telomeres in cancer: tumour suppression and genome instability (2017) · cites this paper as [75]
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“Using this approach, evidence for past telomere crisis has been obtained in CLL as well as in breast cancer, colorectal adenomas and other solid tumours75,77,78.”
From Telomeres in cancer: tumour suppression and genome instability (2017) · cites this paper as [75]
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“Critical telomere shortening (12.8 repeats of repetitive clusters) either as a loss of telomere-capping proteins results to telomere dysfunction with consequent chromosomes fusion and genome instability [22].”
From Markers of cellular senescence. Telomere shortening as a marker of cellular senescence (2016) · cites this paper as [22]
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Cites
Specific Association of Human Telomerase Activity with Immortal Cells and Cancer
Kim, N. W., Piatyszek, M. A., Prowse, K. R., Harley, C. B., West, M. D., Ho, P. L. C., Coviello, G. M., Wright, W. E., Weinrich, S. L., & Shay, J. W. (1994) · Science · doi:10.1126/science.7605428 · Cited by 7,091 · cited 2×
“They occur early in tumor development, after which the genome appears to stabilize with advancing malignancy, roughly coincident with the activation of telomerase (Kim et al. 1994; Chadeneau et al. 1995; Meyerson et al. 1997).”
BackgroundTelomeres shorten during ageing of human fibroblasts
Harley, C. B., Futcher, A. B., & Greider, C. W. (1990) · Nature · doi:10.1038/345458a0 · Cited by 5,750
Characteristics of a human cell line transformed by DNA from human adenovirus type 5
Graham, F. L., Russell, W. C., Smiley, J., & Nairn, R. (1977) · Journal of General Virology · doi:10.1099/0022-1317-36-1-59 · Cited by 4,793
Identification of a specific telomere terminal transferase activity in tetrahymena extracts
Greider, C. W., & Blackburn, E. H. (1985) · Cell · doi:10.1016/0092-8674(85)90170-9 · Cited by 3,400
A DNA damage checkpoint response in telomere-initiated senescence
Fagagna, F. D. D., Reaper, P. M., Clay-Farrace, L., Fiegler, H., Carr, P., von Zglinicki, T., Saretzki, G., Carter, N. P., & Jackson, S. P. (2003) · Nature · doi:10.1038/nature02118 · Cited by 2,917
A Human Cell Line From a Pleural Effusion Derived From a Breast Carcinoma 2
Soule, H. D., Vázquez, J., Long, A., Albert, S. M., & BRENNAN, M. D. (1973) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/51.5.1409 · Cited by 2,452
Meyerson, M., Counter, C. M., Eaton, E. N., Ellisen, L. W., Steiner, P., Caddle, S. D., Ziaugra, L., Beijersbergen, R. L., Davidoff, M. J., Liu, Q., et al. (1997) · Cell · doi:10.1016/s0092-8674(00)80538-3 · Cited by 1,784
TRF2 Protects Human Telomeres from End-to-End Fusions
van Steensel, B., Smogorzewska, A., & de Lange, T. (1998) · Cell · doi:10.1016/s0092-8674(00)80932-0 · Cited by 1,709
DNA Damage Foci at Dysfunctional Telomeres
Takai, H., Smogorzewska, A., & de Lange, T. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00542-6 · Cited by 1,409
Longevity, Stress Response, and Cancer in Aging Telomerase-Deficient Mice
Rudolph, K. L., Chang, S., Lee, H.-W., Blasco, M., Gottlieb, G. J., Greider, C., & DePinho, R. A. (1999) · Cell · doi:10.1016/s0092-8674(00)80580-2 · Cited by 1,349 · cited 2×
“Late-generation telomerase knockout mice ( terc −/− ) show telomere loss, genomic instability, a higher rate of tumor formation, and a lower age of onset (Rudolph et al. 1999; O’Hagan et al. 2002).”
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Mammalian polymerase θ promotes alternative NHEJ and suppresses recombination
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Maciejowski, J., Li, Y., Bosco, N., Campbell, P. J., & de Lange, T. (2015) · Cell · doi:10.1016/j.cell.2015.11.054 · Cited by 675
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Deng, Y., Chan, S. S., & Chang, S. (2008) · Nature Reviews Cancer · doi:10.1038/nrc2393 · Cited by 411
Williams, R. H., Khan, I. M., Richardson, K., Nelson, L., McCarthy, H. E., Analbelsi, T., Singhrao, S. K., Dowthwaite, G. P., Jones, R. E., Baird, D. M., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0013246 · Cited by 406
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Ma, H., Zhou, Z., Wei, S., Liu, Z., Pooley, K. A., Dunning, A. M., Svenson, U., Roos, G., Hosgood, H. D., Shen, M., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0020466 · Cited by 376
“break, causing genome instability and enhancing potential for malignant transformation via fusion-bridge-breakage cycles [56].”
Stepanenko, A. A., & Dmitrenko, V. V. (2015) · Gene · doi:10.1016/j.gene.2015.05.065 · Cited by 356
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Self-citationDicentric breakage at telomere fusionsPreprint
Pobiega, S., & Marcand, S. (2010) · Genes & Development · doi:10.1101/gad.571510 · Cited by 46
DNA Synthesis Generates Terminal Duplications That Seal End-to-End Chromosome Fusions
Lowden, M. R., Flibotte, S., Moerman, D. G., & Ahmed, S. C. (2011) · Science · doi:10.1126/science.1199022 · Cited by 49
Gilbert-Girard, S., Gravel, A., Artusi, S., Richter, S. N., Wallaschek, N., Kaufer, B. B., & Flamand, L. (2017) · Journal of Virology · doi:10.1128/jvi.00402-17 · Cited by 47
Jovanovic, K., Chetty, C. J., Khumalo, T., Dias, B. D. C., Ferreira, E., Malindisa, S. T., Caveney, R. J., Letsolo, B. T., & Weiss, S. F. T. (2015) · Expert Opinion on Therapeutic Patents · doi:10.1517/13543776.2015.1014802 · Cited by 48
Self-citationHigh-throughput single-molecule telomere characterizationPreprint
McCaffrey, J., YOUNG, E. A., Lassahn, K. A., Sibert, J. G., Pastor, S. J., Riethman, H. C., & Xiao, M. (2017) · Genome Research · doi:10.1101/gr.222422.117 · Cited by 51
Liddiard, K., Ruis, B. L., Takasugi, T., Harvey, A., Ashelford, K. E., Hendrickson, E. A., & Baird, D. M. (2016) · Genome Research · doi:10.1101/gr.200840.115 · Cited by 48
Self-citationTelomere fusion threshold identifies a poor prognostic subset of breast cancer patients
Simpson, K., Jones, R. E., Grimstead, J. W., Hills, R., Pepper, C., & Baird, D. M. (2015) · Molecular Oncology · doi:10.1016/j.molonc.2015.02.003 · Cited by 46
Self-citationOh, S., Wang, Y., Zimbric, J., & Hendrickson, E. A. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks1326 · Cited by 46
Changes of telomere status with aging: An update
Ishikawa, N., Nakamura, K., Izumiyama‐Shimomura, N., Aida, J., Matsuda, Y., Arai, T., & Takubo, K. (2016) · Geriatrics and gerontology international/Geriatrics & gerontology international · doi:10.1111/ggi.12772 · Cited by 45
CD57+ Memory T Cells Proliferate In Vivo
Ahmed, R., Miners, K. L., Lahoz-Beneytez, J., Jones, R. E., Roger, L., BABOONIAN, C., Zhang, Y., Wang, E. C. Y., Hellerstein, M. K., McCune, J. M., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108501 · Cited by 43
Self-citationLiu, S.-C., Feng, Y.-L., Sun, X., Chen, R.-D., Liu, Q., Xiao, J., Zhang, J., Huang, Z., Xiang, J.-F., Chen, G., et al. (2022) · Genome biology · doi:10.1186/s13059-022-02736-5 · Cited by 43
Genome stability from the perspective of telomere length
Lu, X., & Liu, L. (2023) · Trends in Genetics · doi:10.1016/j.tig.2023.10.013 · Cited by 44
Lundberg, G., Sehic, D., Länsberg, J., Øra, I., Frigyesi, A., Castel, V., Navarro, S., Piqueras, M., Martinsson, T., Noguera, R., et al. (2011) · Genes Chromosomes and Cancer · doi:10.1002/gcc.20850 · Cited by 43
Subtelomeric regions in mammalian cells are deficient in DNA double-strand break repair
Miller, D. L., Reynolds, G. E., Mejı́a, R., Stark, J. M., & Murnane, J. P. (2011) · DNA repair · doi:10.1016/j.dnarep.2011.03.001 · Cited by 41
Chen, C., Chang, D., Chen, T., Lee, C.-C., Hsieh, H.-H., Huang, F.-C., Huang, K.-F., Guh, J., Lin, J., & Huang, H. (2012) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2012.11.032 · Cited by 39
Mechanisms of telomeric instability
Baird, D. M. (2008) · Cytogenetic and Genome Research · doi:10.1159/000167817 · Cited by 40
Self-citation
Metadata
- Authors
- Capper, R., Britt-Compton, B., Tankimanova, M., Rowson, J., Letsolo, B., Man, S., Haughton, M., & Baird, D. M.
- Affiliations
- Cardiff University (GB)
- Corresponding author
- Baird, Duncan M.
- Venue
- Genes & Development
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2007-10-01
- Volume
- 21
- Issue
- 19
- Pages
- 2495-2508
- ISSN
- 0890-9369 (ISSN-L)
- 1549-5477
- PMC
- PMC1993879
- OpenAlex
- W2159349156
- Cited by
- 294
- References
- 62
- Citations by year
- 2026: 7 · 2025: 7 · 2024: 17 · 2023: 11 · 2022: 18 · 2021: 19 · 2020: 14 · 2019: 8 · 2018: 22 · 2017: 21 · 2016: 16 · 2015: 19 · 2014: 14 · 2013: 13 · 2012: 14
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Genes & Development (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- ORCA Online Research @Cardiff (Cardiff University) (acceptedVersion)
- Funders
- Cancer Research UK
- Medical Research Council
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Telomeres, Telomerase, and Senescence
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA and Nucleic Acid Chemistry
- Keywords
- telomere fusion, telomere shortening, chromosomal instability, non-reciprocal translocation, microhomology-mediated end joining, TRF2, telomerase, carcinogenesis, single-molecule analysis
- MeSH terms
- Base Sequence, Humans, Molecular Sequence Data, Mutagenesis, Insertional, Telomere, Cellular Senescence, Sequence Deletion, Tandem Repeat Sequences, Telomeric Repeat Binding Protein 2, Chromosomal Instability, Cell Line, Tumor
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