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Senescence Induced by Altered Telomere State, Not Telomere Loss
Abstract
Primary human cells in culture invariably stop dividing and enter a state of growth arrest called replicative senescence. This transition is induced by programmed telomere shortening, but the underlying mechanisms are unclear. Here, we report that overexpression of TRF2, a telomeric DNA binding protein, increased the rate of telomere shortening in primary cells without accelerating senescence. TRF2 reduced the senescence setpoint, defined as telomere length at senescence, from 7 to 4 kilobases. TRF2 protected critically short telomeres from fusion and repressed chromosome-end fusions in presenescent cultures, which explains the ability of TRF2 to delay senescence. Thus, replicative senescence is induced by a change in the protected status of shortened telomeres rather than by a complete loss of telomeric DNA.
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In the citing paper
“In addition, the TRF2-dependent suppression of DNA repair within telomeres can yield DDR signaling from telomere-associated damage resulting from causes other than telomere shortening (Karlseder et al. 2002; Fumagalli et al. 2012).”
From Cellular senescence and its effector programs (2014) · cites this paper as Karlseder et al. 2002
In the citing paper
“Furthermore, over-expression of the shelterin subunit telomeric repeat-binding factor 2 (TRF2; also known as TERF2) can delay the onset of senescence44, arguing that the DDR in senescence is due to an insufficient loading of shelterin at the shortened telomeres.”
From Telomeres in cancer: tumour suppression and genome instability (2017) · cites this paper as [44]
In the citing paper
“In agreement, TRF2 overexpression delays replicative senescence onset [101], indicating that TRF2 capacity to sequester the telomere terminus via the t-loop conformation [88] might suppress the DNA damage signal from too short telomere ends and protect them from ATM signaling.”
From Mechanisms and Regulation of Cellular Senescence (2021) · cites this paper as [101]
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Cites
Telomeres 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
Extension of Life-Span by Introduction of Telomerase into Normal Human Cells
Bodnar, A. G., Ouellette, M., Frolkis, M., Holt, S. E., Chiu, C.-P., Morin, G. B., Harley, C. B., Shay, J. W., Lichtsteiner, S., & Wright, W. E. (1998) · Science · doi:10.1126/science.279.5349.349 · Cited by 4,975
Mammalian Telomeres End in a Large Duplex Loop
Griffith, J. D., Comeau, L., Rosenfield, S., Stansel, R. M., Bianchi, A., Moss, H., & de Lange, T. (1999) · Cell · doi:10.1016/s0092-8674(00)80760-6 · Cited by 2,447
Counter, C. M., Avilion, A. A., LeFeuvre, C. E., Stewart, N. G., Greider, C. W., Harley, C. B., & Bacchetti, S. (1992) · The EMBO Journal · doi:10.1002/j.1460-2075.1992.tb05245.x · Cited by 2,096
Olovnikov (1973) · doi:10.1016/0022-5193(73)90198-7 · Cited by 1,847
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
Self-citationWATSON, J. D. (1972) · Nature New Biology · doi:10.1038/newbio239197a0 · Cited by 1,632
Control of telomere length by the human telomeric protein TRF1
van Steensel, B., & de Lange, T. (1997) · Nature · doi:10.1038/385740a0 · Cited by 1,219
p53- and ATM-Dependent Apoptosis Induced by Telomeres Lacking TRF2
Karlseder, J., Broccoli, D., Dai, Y., Hardy, S., & de Lange, T. (1999) · Science · doi:10.1126/science.283.5406.1321 · Cited by 1,086
Self-citationMakarov, V. L., Hirose, Y., & Langmore, J. P. (1997) · Cell · doi:10.1016/s0092-8674(00)81908-x · Cited by 959
Research works printed but not linked: 2
- Supplementary material is available on Science Online at www.sciencemag.org/cgi/content/full/295/5564/2446/DC1.
- Hinds P. W., et al., Cell Growth Differ. 1, 571 (1990).
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Dong, W., Shen, R., Wang, Q., Gao, Y., Qi, X., Jiang, H., Yao, J., Lin, X., Wu, Y., & Wang, L. (2009) · Cancer Biology & Therapy · doi:10.4161/cbt.8.22.9880 · Cited by 34
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Harrington, L. A. (2003) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2003.12.007 · Cited by 35
Vukićević, V., Jauch, A. S., Dinger, T. C., Gebauer, L., Hornich, V., Bornstein, S. R., Ehrhart‐Bornstein, M., & Müller, A. M. (2010) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2010.01.001 · Cited by 33
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Satoh, M., Nasu, T., Takahashi, Y., Osaki, T., Hitomi, S., Morino, Y., & Nakamura, M. (2017) · Clinical Science · doi:10.1042/cs20170242 · Cited by 27
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(2009) · Methods in molecular biology · doi:10.1007/978-1-59745-363-9 · Cited by 20
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Metadata
- Authors
- Karlseder, J., Smogorzewska, A., & de Lange, T.
- Affiliations
- Rockefeller University (US)
- Laboratory for Cell Biology and Genetics, The Rockefeller University, 1230 York Avenue, New York, NY 10021, USA.
- Venue
- Science
- Published
- 2002-03-29
- Volume
- 295
- Issue
- 5564
- Pages
- 2446-2449
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2088926897
- Cited by
- 796
- References
- 25
- Citations by year
- 2026: 10 · 2025: 11 · 2024: 22 · 2023: 11 · 2022: 14 · 2021: 22 · 2020: 18 · 2019: 19 · 2018: 26 · 2017: 22 · 2016: 20 · 2015: 29 · 2014: 24 · 2013: 22 · 2012: 35
- FWCI
- 47.76
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute on Aging (AG 16643)
- National Cancer Institute (R01CA076027, CA76027)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Telomeres, Telomerase, and Senescence
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA and Nucleic Acid Chemistry
- Keywords
- replicative senescence, telomere shortening, TRF2, telomere length, telomere fusion, primary human cells, growth arrest
- MeSH terms
- Antigens, Polyomavirus Transforming, Cell Division, Cell Line, Cells, Cultured, DNA, DNA-Binding Proteins, Humans, Oncogene Proteins, Viral, Repressor Proteins, Retroviridae, Transformation, Genetic, Tumor Suppressor Protein p53, Retinoblastoma Protein, Telomere, Cellular Senescence, Telomeric Repeat Binding Protein 2, Papillomavirus E7 Proteins
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