Cited by 649DNA Repair MechanismsCRISPR and Genetic EngineeringEffects of Radiation Exposure

The DOI matches its Crossref record; 27 of the 29 references it cites were found in a registry or an index, and 2 are not checked yet.

Homology-directed repair is a major double-strand break repair pathway in mammalian cells

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Liang, Feng, Han, Mingguang, Romanienko, Peter J., Jasin, Maria·1998·Proceedings of the National Academy of Sciences

Abstract

Mammalian cells have been presumed to repair potentially lethal chromosomal double-strand breaks (DSBs) in large part by processes that do not require homology to the break site. This contrasts with Saccharomyces cerevisiae where the major DSB repair pathway is homologous recombination. Recently, it has been determined that DSBs in genomic DNA in mammalian cells can stimulate homologous recombination as much as 3 or 4 orders of magnitude, suggesting that homology-directed repair may play an important role in the repair of chromosomal breaks. To determine whether mammalian cells use recombinational repair at a significant level, we have analyzed the spectrum of repair events at a defined chromosomal break by using direct physical analysis of repair products. When an endonuclease-generated DSB is introduced into one of two direct repeats, homologous repair is found to account for 30–50% of observed repair events. Both noncrossover and deletional homologous repair products are detected, at approximately a 1:3 ratio. These results demonstrate the importance of homologous recombination in the repair of DSBs in mammalian cells. In the remaining observed repair events, DSBs are repaired by nonhomologous processes. The nonhomologous repair events generally result in small deletions or insertions at the break site, although a small fraction of events result in larger chromosomal rearrangements. Interestingly, in two insertions, GT repeats were integrated at one of the broken chromosome ends, suggesting that DSB repair can contribute to the spread of microsatellite sequences in mammalian genomes.

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Research works printed but not linked: 3

  1. T D Petes, R E Malone, L S Symington Recombination in Yeast (Cold Spring Harbor Lab. Press, Plainview, NY, 1991).
  2. 10.1128/mcb.10.1.103-112.1990 · DOI
  3. S A Schichman, M A Caligiuri, M P Strout, S L Carter, Y Gu, E Canaani, C D Bloomfield, C M Croce Cancer Res 54, 4277–4280 (1994).

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Metadata

Authors
Liang, F., Han, M., Romanienko, P. J., & Jasin, M.
Affiliations
Cornell University (US)
Corresponding author
Jasin, Maria
Venue
Proceedings of the National Academy of Sciences
Published
1998-04-28
Volume
95
Issue
9
Pages
5172-5177
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2168809955
Cited by
649
References
27
Citations by year
2026: 5 · 2025: 11 · 2024: 18 · 2023: 12 · 2022: 21 · 2021: 25 · 2020: 19 · 2019: 17 · 2018: 13 · 2017: 16 · 2016: 13 · 2015: 13 · 2014: 12 · 2013: 11 · 2012: 13
FWCI
15.73
Type
journal article
Language
en
Open access
Locations
  • Proceedings of the National Academy of Sciences (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • American Cancer Society
  • National Institutes of Health
  • National Institute of General Medical Sciences (GM54688)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › CRISPR and Genetic Engineering
  • Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Effects of Radiation Exposure
Keywords
homology-directed repair, DNA double-strand break repair, homologous recombination, non-homologous end joining, mammalian cells, chromosomal breaks, chromosomal rearrangements
MeSH terms
Animals, Cells, Cultured, DNA Damage, DNA Repair, Gene Conversion, Cricetinae, Recombination, Genetic, Sequence Homology, Nucleic Acid, Restriction Mapping, CHO Cells, Sequence Deletion

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