The DOI matches its Crossref record; 33 of the 33 references it cites were found in a registry or an index.
Preferential Accumulation of Single-Stranded Regions in Telomeres of Human Fibroblasts
Open accessAbstract
We have demonstrated recently that chronic hyperoxic treatment accelerates the rate of aging of fibroblasts and the rate of telomere shortening in parallel. It was hypothesized that accelerated telomere shortening is due to preferential accumulation of oxidative damage in telomeres. To test this hypothesis, we measured the accumulation of sites sensitive to S1 nuclease treatment in telomeres, in minisatellites, and in the bulk of the genome of fibroblasts under different models of oxidative stress as well as after treatment with the alkylating agent, N-methyl-N'-nitro-N-nitrosoguanidine. A comparison with qualitative data obtained by alkaline electrophoresis reveals that the sites transferred to double-strand breaks by treatment with low concentrations of S1 nuclease are, in fact, single-stranded regions in the DNA. These regions may resemble single-stranded overhangs, gaps, or conventional single-strand breaks. The frequency of single-stranded regions is significantly higher in telomeres than in minisatellites or in the bulk of the genome under all conditions tested. Those regions induced in minisatellites or in the overall genome by a bolus dose of hydrogen peroxide are completely repaired within 24 h. On the other hand, 50 +/- 12% of H2O2-induced single-stranded regions remain unrepaired for at least 19 days in telomeres of human fibroblasts, leading to a significant increase of the telomeric steady-state level of these lesions. This preferential accumulation might significantly contribute to telomere shortening.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“As telomere DNA is particularly sensitive to oxidative damage (Oikawa & Kawanishi, 1999) and single‐strand breaks or other stress‐induced lesions at telomeres are inefficiently repaired (Petersen et al., 1998)”
From P66SHC deletion improves fertility and progeric phenotype of late-generation TERC-deficient mice but not their short lifespan (2016) · cites this paper as Petersen et al., 1998
In the citing paper
“single-stranded breaks have been shown to preferentially accumulate at telomeres in conditions of mild oxidative stress, and such lesions lead to replication fork stalling, resulting in incomplete replication of chromosome ends and thus accelerated telomere shortening (Petersen et al., 1998, von Zglinicki, 2000).”
From Telomeres and cell senescence—size matters not (2017) · cites this paper as Petersen et al., 1998
In the citing paper
“Many studies associate the presence of a great amount of mitochondrial ROS with accumulated single-strand breaks in telomere regions, thus accelerating telomere erosion and cellular senescence [106,107].”
From Role of Age-Related Mitochondrial Dysfunction in Sarcopenia (2020) · cites this paper as [106]
Citations
Cites
The limited in vitro lifetime of human diploid cell strains
Hayflick, L. (1965) · Experimental Cell Research · doi:10.1016/0014-4827(65)90211-9 · Cited by 5,876
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
The RNA Component of Human Telomerase
Feng, J., Funk, W. D., Wang, S.-S., Weinrich, S. L., Avilion, A. A., Chiu, C.-P., Adams, R. R., Chang, E., Allsopp, R. C., Yu, J., et al. (1995) · Science · doi:10.1126/science.7544491 · Cited by 2,227
Telomere loss: mitotic clock or genetic time bomb?
Harley, C. B. (1991) · Mutation Research/DNAging · doi:10.1016/0921-8734(91)90018-7 · Cited by 1,139
Oxidative damage to DNA during aging: 8-hydroxy-2'-deoxyguanosine in rat organ DNA and urine.
Fraga, C. G., Shigenaga, M. K., Park, J. W., Degan, P., & Ames, B. N. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.12.4533 · Cited by 1,106
Makarov, V. L., Hirose, Y., & Langmore, J. P. (1997) · Cell · doi:10.1016/s0092-8674(00)81908-x · Cited by 959
Mild hyperoxia shortens telomeres and inhibits proliferation of fibroblasts: a model for senescence?
von Zglinicki, T., Saretzki, G., Döcke, W., & Lotze, C. (1995) · Experimental Cell Research · doi:10.1006/excr.1995.1305 · Cited by 856
Self-citationOxidative DNA damage and senescence of human diploid fibroblast cells.
Chen, Q., Fischer, A., Reagan, J. D., Yan, L. J., & Ames, B. N. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.10.4337 · Cited by 720
Henderson, E. A., Hardin, C. C., Walk, S. K., Tinoco, I., & Blackburn, E. H. (1987) · Cell · doi:10.1016/0092-8674(87)90577-0 · Cited by 684
Telomerase activity in normal leukocytes and in hematologic malignancies
Counter, C. M., Gupta, J., Harley, C., Leber, B. F., & Bacchetti, S. (1995) · Blood · doi:10.1182/blood.v85.9.2315.bloodjournal8592315 · Cited by 604
Telomere Shortening Is Associated with Cell Division in Vitro and in Vivo
Allsopp, R. C., Chang, E., Kashefi-Aazam, M., Rogaev, E. I., Piatyszek, M. A., Shay, J. W., & Harley, C. B. (1995) · Experimental Cell Research · doi:10.1006/excr.1995.1306 · Cited by 533
Härle-Bachor, C., & Boukamp, P. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.13.6476 · Cited by 492
Low oxygen concentration extends the lifespan of cultured human diploid cells
Packer, L., & FUEHR, K. (1977) · Nature · doi:10.1038/267423a0 · Cited by 393
The terminal DNA structure of mammalian chromosomes
McElligott, R., & Wellinger, R. J. (1997) · The EMBO Journal · doi:10.1093/emboj/16.12.3705 · Cited by 379
DNA damage and repair in telomeres: relation to aging
Kruk, P. A., Rampino, N. J., & Bohr, V. A. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.1.258 · Cited by 333
Evidence for a New Step in Telomere Maintenance
Wellinger, R. J., Ethier, K., Labrecque, P., & Zakian, V. A. (1996) · Cell · doi:10.1016/s0092-8674(00)81120-4 · Cited by 308
Detection of Telomerase Activity in Malignant and Nonmalignant Skin Conditions
Taylor, R. S., Ramirez, R. D., Ogoshi, M., Chaffins, M. L., Piatyszek, M. A., & Shay, J. W. (1996) · Journal of Investigative Dermatology · doi:10.1111/1523-1747.ep12345811 · Cited by 265
Reconstitution of the DNA base excision—repair pathway
Dianov, G. L., & Lindahl, T. L. (1994) · Current Biology · doi:10.1016/s0960-9822(00)00245-1 · Cited by 251
Telomere positional effects and the regulation of cellular senescence
Wright, W. E., & Shay, J. W. (1992) · Trends in Genetics · doi:10.1016/0168-9525(92)90232-s · Cited by 250
Radiation Induced Strand Breakage in DNA from Mammalian Cells
Ahnström, G., & Erixon, K. (1973) · International Journal of Radiation Biology and Related Studies in Physics Chemistry and Medicine · doi:10.1080/09553007314550311 · Cited by 223
Cell cycle-regulated generation of single-stranded G-rich DNA in the absence of telomerase
Dionne, I., & Wellinger, R. J. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.24.13902 · Cited by 209
Freeman, S. E., Blackett, A. D., Monteleone, D. C., Setlow, R. B., Sutherland, B. M., & Sutherland, J. C. (1986) · Analytical Biochemistry · doi:10.1016/0003-2697(86)90599-3 · Cited by 198
Accelerated Telomere Shortening in Fibroblasts After Extended Periods of Confluency
Sitte, N. (1998) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(97)00363-8 · Cited by 162
Optimized oligonucleotide probes for DNA fingerprinting
Schäfer, R., Zischler, H., Birsner, U., Becker, A., & Epplen, J. T. (1988) · Electrophoresis · doi:10.1002/elps.1150090804 · Cited by 145
Zischler, H., Nanda, I., Sch�fer, R., Schmid, M., & Epplen, J. T. (1989) · Human Genetics · doi:10.1007/bf00291160 · Cited by 109
Лукаш, Л. Л., Boldt, J., Pegg, A. E., Dolan, M. E., Maher, V. M., & McCormick, J. J. (1991) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/0027-5107(91)90196-u · Cited by 68
Nick translation—a new assay for monitoring dna damage and repair in cultured human fibroblasts
Snyder, R. D., & Matheson, D. W. (1985) · Environmental Mutagenesis · doi:10.1002/em.2860070304 · Cited by 65
Wassermann, K., Kohn, K. W., & Bohr, V. A. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)77434-6 · Cited by 63
Telomerase: immortality enzyme or oncogene?
Kipling, D. (1995) · Nature Genetics · doi:10.1038/ng0295-104 · Cited by 41
Zischler, H., Kammerbauer, C., Studer, R., Grzeschik, K.-H., & Epplen, J. T. (1992) · Genomics · doi:10.1016/0888-7543(92)90011-g · Cited by 39
Formation of novel hairpin structures by telemeric C-strand oligonucleotides
Ahmed, S. C., & Henderson, E. R. (1992) · Nucleic Acids Research · doi:10.1093/nar/20.3.507 · Cited by 35
[Molecular mechanisms of senescence in cell culture].
von Zglinicki, T., & Saretzki, G. C. (1997) · PubMed · Cited by 10
Self-citationTelomerase activity in human germline and embryonic tissues and cells
Wright, W. E., Piatyszek, M. A., Rainey, W. E., Byrd, W., & Shay, J. W. (1996) · Developmental Genetics · doi:10.1002/(sici)1520-6408(1996)18:2
Flagged first, then by citations
Research works printed but not linked: 1
- von Zglinicki, 1997, Die molekularen Mechanismen der Seneszenz in Zellkultur, Z. Gerontol. Geriatr., 30, 24
Cited by
Sorted by citations
Oxidative stress shortens telomeres
von Zglinicki, T. (2002) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(02)02110-2 · Cited by 2,524
Blackburn, E. H., Epel, E. S., & Lin, J. (2015) · Science · doi:10.1126/science.aab3389 · Cited by 1,596
Mitochondria, oxygen free radicals, disease and ageing
Raha, S., & Robinson, B. H. (2000) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(00)01674-1 · Cited by 1,066
Trends in oxidative aging theories
Muller, F. L., Lustgarten, M. S., Jang, Y., Richardson, A., & Van Remmen, H. (2007) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2007.03.034 · Cited by 1,053
Hewitt, G., Jurk, D., Marques, F. D. M., Correia-Melo, C., Hardy, T., Gackowska, A., Anderson, R., Taschuk, M., Mann, J., & Passos, J. F. (2012) · Nature Communications · doi:10.1038/ncomms1708 · Cited by 908
Metadata
- Authors
- Petersen, S., Saretzki, G., & Zglinicki, T. V.
- Affiliations
- Humboldt-Universität zu Berlin (DE)
- Corresponding author
- Zglinicki, Thomas von
- Venue
- Experimental Cell Research
- Publisher
- Elsevier BV
- Published
- 1998-02
- Volume
- 239
- Issue
- 1
- Pages
- 152-160
- ISSN
- 0014-4827 (ISSN-L)
- OpenAlex
- W2037480531
- Cited by
- 427
- References
- 33
- Citations by year
- 2026: 1 · 2025: 10 · 2024: 9 · 2023: 17 · 2022: 15 · 2021: 14 · 2020: 14 · 2019: 19 · 2018: 18 · 2017: 14 · 2016: 23 · 2015: 15 · 2014: 16 · 2013: 17 · 2012: 20
- FWCI
- 7.99
- Type
- journal article
- Language
- en
- Open access
- green
- doi.org
- Locations
- Experimental Cell Research (publishedVersion)
- PubMed (publishedVersion)
- Newcastle University ePrints (Newcastle Univesity)
- 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 › Aging › Genetics, Aging, and Longevity in Model Organisms
- Keywords
- telomeres, telomere shortening, oxidative DNA damage, hydrogen peroxide, S1 nuclease, minisatellites, N-methyl-N'-nitro-N-nitrosoguanidine, alkylating agents, DNA repair, human fibroblasts, hyperoxia, aging
- MeSH terms
- Cell Line, DNA, Fibroblasts, Humans, Methylnitronitrosoguanidine, Single-Strand Specific DNA and RNA Endonucleases, Telomere, Minisatellite Repeats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review