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The Mechanism of Double-Strand DNA Break Repair by the Nonhomologous DNA End-Joining Pathway
Open accessAbstract
Double-strand DNA breaks are common events in eukaryotic cells, and there are two major pathways for repairing them: homologous recombination (HR) and nonhomologous DNA end joining (NHEJ). The various causes of double-strand breaks (DSBs) result in a diverse chemistry of DNA ends that must be repaired. Across NHEJ evolution, the enzymes of the NHEJ pathway exhibit a remarkable degree of structural tolerance in the range of DNA end substrate configurations upon which they can act. In vertebrate cells, the nuclease, DNA polymerases, and ligase of NHEJ are the most mechanistically flexible and multifunctional enzymes in each of their classes. Unlike repair pathways for more defined lesions, NHEJ repair enzymes act iteratively, act in any order, and can function independently of one another at each of the two DNA ends being joined. NHEJ is critical not only for the repair of pathologic DSBs as in chromosomal translocations, but also for the repair of physiologic DSBs created during variable (diversity) joining [V(D)J] recombination and class switch recombination (CSR). Therefore, patients lacking normal NHEJ are not only sensitive to ionizing radiation (IR), but also severely immunodeficient.
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“Breakpoints of some non-recurrent deletion CNVs have sequences with very short (2–20 basepairs) stretches of nucleotide identity. These are predicted to be formed by an alternative microhomology mediated end joining (MMEJ) mechanism (Lieber, 2010).”
From CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics (2012) · cites this paper as Lieber, 2010
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“DNA double-strand break repair or non-homologous end joining (NHEJ) repairs breaks induced by ionizing radiation (IR), oxidative free radicals, misappropriate enzymatic action at sensitive sites, inhibition of topoisomerases, and other mechanical stresses [54].”
From Integration of DNA damage and repair with murine double-minute 2 (Mdm2) in tumorigenesis (2012) · cites this paper as [54]
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Citations
Cites
Hydroperoxide metabolism in mammalian organs.
Chance, B., Sies, H., & Boveris, A. (1979) · Physiological Reviews · doi:10.1152/physrev.1979.59.3.527 · Cited by 5,827
Friedberg, E. C., Walker, G. C., Siede, W., Wood, R. D., Schultz, R. A., & Ellenberger, T. (2005) · doi:10.1128/9781555816704 · Cited by 5,683
Mechanism of Eukaryotic Homologous Recombination
Filippo, J. S., Sung, P., & Klein, H. L. (2008) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.77.061306.125255 · Cited by 1,766
Conserved modes of recruitment of ATM, ATR and DNA-PKcs to sites of DNA damage
Falck, J., Coates, J., & Jackson, S. P. (2005) · Nature · doi:10.1038/nature03442 · Cited by 1,304
Meiotic Chromosomes: Integrating Structure and Function
Zickler, D., & Kleckner, N. E. (1999) · Annual Review of Genetics · doi:10.1146/annurev.genet.33.1.603 · Cited by 1,256
Structure of the Ku heterodimer bound to DNA and its implications for double-strand break repair
Walker, J. R., Corpina, R. A., & Goldberg, J. D. (2001) · Nature · doi:10.1038/35088000 · Cited by 1,216
Walker, E. H., Pacold, M. E., Perišić, O., Stephens, L., Hawkins, P. T., Wymann, M. P., & Williams, R. L. (2000) · Molecular Cell · doi:10.1016/s1097-2765(05)00089-4 · Cited by 1,211
Ma, Y., Pannicke, U., Schwarz, K., & Lieber, M. R. (2002) · Cell · doi:10.1016/s0092-8674(02)00671-2 · Cited by 1,166
Self-citationATM and DNA-PK Function Redundantly to Phosphorylate H2AX after Exposure to Ionizing Radiation
Stiff, T., O’Driscoll, M., Rief, N., Iwabuchi, K., Löbrich, M., & Jeggo, P. A. (2004) · Cancer Research · doi:10.1158/0008-5472.can-03-3207 · Cited by 1,050
The Mechanism and Regulation of Chromosomal V(D)J Recombination
Bassing, C. H., Swat, W., & Alt, F. W. (2002) · Cell · doi:10.1016/s0092-8674(02)00675-x · Cited by 1,006
Research works printed but not linked: 5
- Martin GM, 1985, Isr. J. Med. Sci., 21, 296
- Wilson TE, 2009, Wiley Encyclopedia of Chemical Biology, 3, 423
- Welzel N, 2001, Cancer Res., 61, 1629
- van der Burg M, 2009, J. Clin. Investig., 119, 91
- Kornberg A, 1992, DNA Replication
Cited by
Sorted by citations
Items 301–400 of 1,005
Li, X., Li, G., Fu, J. L., Fu, Y.-W., Zhang, L., Chen, W., Arakaki, C., Zhang, J., Wen, W., Zhao, M., et al. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky804 · Cited by 113
Homologous Recombination Deficiencies and Hereditary Tumors
Yamamoto, H., & Hirasawa, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms23010348 · Cited by 128
Poot, M., & Haaf, T. (2015) · Molecular Syndromology · doi:10.1159/000438812 · Cited by 116
PAXX Is an Accessory c-NHEJ Factor that Associates with Ku70 and Has Overlapping Functions with XLF
Tadi, S. K., Tellier-Lebègue, C., Nemoz, C., Drevet, P., Audebert, S., Roy, S., Meek, K., Charbonnier, J., & Modesti, M. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.09.026 · Cited by 115
In vivo genome editing via the HITI method as a tool for gene therapy
Suzuki, K., & Belmonte, J. C. I. (2017) · Journal of Human Genetics · doi:10.1038/s10038-017-0352-4 · Cited by 122
DNA polymerase θ (POLQ) is important for repair of DNA double-strand breaks caused by fork collapse
Wang, Z., Song, Y., Li, S., Kurian, S. M., Xiang, R., Chiba, T., & Wu, X. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.005188 · Cited by 120
Microhomology Directs Diverse DNA Break Repair Pathways and Chromosomal Translocations
Villarreal, D. D., Lee, K., Deem, A. K., Shim, E. Y., Malkova, A., & Lee, S. E. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1003026 · Cited by 124
de Bruijn, S. E., Fiorentino, A., Ottaviani, D., Fanucchi, S., Melo, U. S., Corral-Serrano, J. C., Mulders, T. W. F., Georgiou, M., Rivolta, C., Pontikos, N., et al. (2020) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2020.09.002 · Cited by 109
Kinase-dead ATM protein causes genomic instability and early embryonic lethality in mice
Yamamoto, K., Wang, Y., Jiang, W., Liu, X., Dubois, R. L., Lin, C., Ludwig, T., Bakkenist, C. J., & Zha, S. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201204098 · Cited by 118
Carmona, L. M., & Schatz, D. G. (2016) · FEBS Journal · doi:10.1111/febs.13990 · Cited by 113
Hsp90: A New Player in DNA Repair?
Pennisi, R., Ascenzi, P., & Di Masi, A. (2015) · Biomolecules · doi:10.3390/biom5042589 · Cited by 112
XLF and APLF bind Ku80 at two remote sites to ensure DNA repair by non-homologous end joining
Nemoz, C., Ropars, V., Frit, P., Gontier, A., Drevet, P., Yu, J., Guérois, R., Pitois, A., Comte, A., Delteil, C., et al. (2018) · Nature Structural & Molecular Biology · doi:10.1038/s41594-018-0133-6 · Cited by 121
White, R. R., Milholland, B., de Bruin, A., Curran, S., Laberge, R.-M., van Steeg, H., Campisi, J., Maslov, A. Y., & Vijg, J. (2015) · Nature Communications · doi:10.1038/ncomms7790 · Cited by 107
Lorenzo, S. B. D., Patel, A. G., Hurley, R. M., & Kaufmann, S. H. (2013) · Frontiers in Oncology · doi:10.3389/fonc.2013.00228 · Cited by 116
Beck, C., Boehler, C., Guirouilh‐Barbat, J., Bonnet, M.-E., Illuzzi, G., Rondé, P., Gauthier, L., Magroun, N., Rajendran, A., López, B. S., et al. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku174 · Cited by 126
Nair, N., Shoaib, M., & Sørensen, C. S. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18071486 · Cited by 117
Efficient induction of heritable inversions in plant genomes using the CRISPR /Cas system
Schmidt, C., Pacher, M., & Puchta, H. (2019) · The Plant Journal · doi:10.1111/tpj.14322 · Cited by 111
Regulation of DNA Repair Mechanisms: How the Chromatin Environment Regulates the DNA Damage Response
Stadler, J., & Richly, H. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18081715 · Cited by 110
H3K36me3, message from chromatin to DNA damage repair
Sun, Z., Zhang, Y., Jia, J., Fang, Y., Tang, Y., Wu, H., & Fang, D. (2020) · Cell & Bioscience · doi:10.1186/s13578-020-0374-z · Cited by 109
Kass, E. M., Helgadottir, H. R., Chen, C.-C., Barbera, M. A., Wang, R., Westermark, U., Ludwig, T., Moynahan, M. E., & Jasin, M. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1216824110 · Cited by 110
Soni, A., Siemann, M., Grabos, M., Murmann-Konda, T., Pantelias, G. E., & Iliakis, G. E. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku298 · Cited by 117
Editing Transgenic DNA Components by Inducible Gene Replacement in Drosophila melanogaster
Lin, C., & Potter, C. J. (2016) · Genetics · doi:10.1534/genetics.116.191783 · Cited by 103
A Mechanism to Minimize Errors during Non-homologous End Joining
Stinson, B. M., Moreno, A., Walter, J. C., & Loparo, J. J. (2019) · Molecular Cell · doi:10.1016/j.molcel.2019.11.018 · Cited by 108
Horta, F., Catt, S. L., Ramachandran, P., Vollenhoven, B. J., & Temple-Smith, P. D. (2019) · Human Reproduction · doi:10.1093/humrep/dez308 · Cited by 124
Site-specific recombinases: molecular machines for the Genetic Revolution
Olorunniji, F. J., Rosser, S. J., & Stark, W. M. (2016) · Biochemical Journal · doi:10.1042/bj20151112 · Cited by 107
Jubair, L., Fallaha, S., & McMillan, N. A. J. (2019) · Molecular Therapy · doi:10.1016/j.ymthe.2019.08.012 · Cited by 107
Interplays between ATM/Tel1 and ATR/Mec1 in sensing and signaling DNA double-strand breaks
Gobbini, E., Cesena, D., Galbiati, A., Lockhart, A., & Longhese, M. P. (2013) · DNA Repair · doi:10.1016/j.dnarep.2013.07.009 · Cited by 98
The Intertwined Roles of Transcription and Repair Proteins
Fong, Y. W., Cattoglio, C., & Tjian, R. (2013) · Molecular Cell · doi:10.1016/j.molcel.2013.10.018 · Cited by 106
Rosa, M., Harder, M. V., Cigliano, R. A., Schlögelhofer, P., & Scheid, O. M. (2013) · The Plant Cell · doi:10.1105/tpc.112.104067 · Cited by 109
A noncatalytic function of the ligation complex during nonhomologous end joining
Jessica, C., Frit, P., Bombarde, O., Salles, B., Négrel, A., Bernard, S., Jeggo, P. A., Lieber, M. R., Modesti, M., & Calsou, P. (2013) · The Journal of Cell Biology · doi:10.1083/jcb.201203128 · Cited by 105
Self-citationA quick guide to CRISPR sgRNA design tools
Brazelton, A., Zarecor, S., Wright, D. A., Wang, Y., Liu, J., Chen, K., Yang, B., & Lawrence‐Dill, C. J. (2015) · GM crops & food · doi:10.1080/21645698.2015.1137690 · Cited by 108
ATM Deficiency Is Associated with Sensitivity to PARP1- and ATR Inhibitors in Lung Adenocarcinoma
Schmitt, A., Knittel, G., Welcker, D., Yang, T.-P., George, J., Nowak, M., Leeser, U., Büttner, R., Perner, S., Peifer, M., et al. (2017) · Cancer Research · doi:10.1158/0008-5472.can-16-3398 · Cited by 109
BRCA Mutations in Prostate Cancer: Assessment, Implications and Treatment Considerations
Shah, S., Rachmat, R., Enyioma, S., Ghose, A., Revythis, A., & Boussios, S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222312628 · Cited by 113
Programmable Genome Editing Tools and their Regulation for Efficient Genome Engineering
Guha, T. K., Wai, A., & Hausner, G. (2017) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2016.12.006 · Cited by 117
Acquired genetic changes in human pluripotent stem cells: origins and consequences
Halliwell, J. A., Barbaric, I., & Andrews, P. W. (2020) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-020-00292-z · Cited by 108
Gunn, A., Bennardo, N., Cheng, A., & Stark, J. M. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.309252 · Cited by 106
Resources for the design of CRISPR gene editing experiments
Graham, D. B., & Root, D. E. (2015) · Genome biology · doi:10.1186/s13059-015-0823-x · Cited by 108
Cell cycle-dependent control of homologous recombination
Zhao, X., Wei, C., Li, J., Xing, P., Li, J., Zheng, S., & Chen, X. (2017) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmx055 · Cited by 113
Comparison of the Feasibility, Efficiency, and Safety of Genome Editing Technologies
Castro, N. G. G., Bjelic, J., Malhotra, G., Huang, C., & Alsaffar, S. H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910355 · Cited by 110
The Hallmarks of Cancer from a Redox Perspective
Hornsveld, M., & Dansen, T. B. (2016) · Antioxidants and Redox Signaling · doi:10.1089/ars.2015.6580 · Cited by 105
Enabling functional genomics with genome engineeringPreprint
Hilton, I. B., & Gersbach, C. A. (2015) · Genome Research · doi:10.1101/gr.190124.115 · Cited by 106
Lee, Y. Y., Yu, Y., Gunawardena, H. P., Xie, L., & Chen, X. N. (2012) · Cell Death and Disease · doi:10.1038/cddis.2012.76 · Cited by 100
DNA repair genes are selectively mutated in diffuse large B cell lymphomas
de Miranda, N. F. C. C., Peng, R., Georgiou, K. E., Wu, C., Falk-Sörqvist, E., Berglund, M., Chen, L., Gao, Z., Lagerstedt‐Robinson, K., Lisboa, S., et al. (2013) · The Journal of Experimental Medicine · doi:10.1084/jem.20122842 · Cited by 108
Pyndiah, S., Tanida, S., Ahmed, K. M., Cassimere, E. K., Choe, C., & Sakamuro, D. (2011) · Science Signaling · doi:10.1126/scisignal.2001556 · Cited by 108
Targeting PARP proteins in acute leukemia: DNA damage response inhibition and therapeutic strategies
Padella, A., di Rorà, A. G. L., Marconi, G., Ghetti, M., Martinelli, G., & Simonetti, G. (2022) · Journal of Hematology & Oncology · doi:10.1186/s13045-022-01228-0 · Cited by 100
Chen, Y., Zhao, Y., Yang, X., Ren, X., Huang, S., Gong, S., Tan, X.-R., Li, J., He, S., Li, Y., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-28158-2 · Cited by 102
Rad51 and BRCA2 - New Molecular Targets for Sensitizing Glioma Cells to Alkylating Anticancer Drugs
Quirós, S., Roos, W. P., & Kaina, B. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027183 · Cited by 106
NHEJ and its backup pathways in chromosomal translocations
Lieber, M. R. (2010) · Nature Structural & Molecular Biology · doi:10.1038/nsmb0410-393 · Cited by 102
Self-citationSchwer, B., Wei, P., Chang, A. N., Kao, J., Du, Z., Meyers, R. M., & Alt, F. W. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1525564113 · Cited by 105
Timing of DNA damage responses impacts persistence to fluoroquinolones
Mok, W. W. K., & Brynildsen, M. P. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1804218115 · Cited by 103
The DNA damage response during mitosis
Heijink, A. M., Krajewska, M., & van Vugt, M. A. T. M. (2013) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2013.07.003 · Cited by 107
Tapping natural reservoirs of homing endonucleases for targeted gene modification
Takeuchi, R., Lambert, A. R., Mak, A. N.-S., Jacoby, K., Dickson, R. J., Gloor, G. B., Scharenberg, A. M., Edgell, D. R., & Stoddard, B. L. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1107719108 · Cited by 100
Controlling DNA-end resection: a new task for CDKs
Ferretti, L. P., Lafranchi, L., & Sartori, A. A. (2013) · Frontiers in Genetics · doi:10.3389/fgene.2013.00099 · Cited by 112
How cancer cells hijack DNA double-strand break repair pathways to gain genomic instability
Jeggo, P. A., & Löbrich, M. (2015) · Biochemical Journal · doi:10.1042/bj20150582 · Cited by 108
Gene therapy for visual loss: Opportunities and concerns
Lee, J. H., Wang, J.-H., Chen, J., Li, F., Edwards, T. L., Hewitt, A. W., & Liu, G. (2018) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2018.08.003 · Cited by 103
Guerra, L., Guidi, R., & Frisan, T. (2011) · FEBS Journal · doi:10.1111/j.1742-4658.2011.08125.x · Cited by 102
Inhibition of nonhomologous end joining to increase the specificity of CRISPR /Cas9 genome editing
Vartak, S. V., & Raghavan, S. C. (2015) · FEBS Journal · doi:10.1111/febs.13416 · Cited by 100
Coupling endonucleases with DNA end–processing enzymes to drive gene disruption
Certo, M. T., Gwiazda, K., Kuhar, R., Sather, B. D., Curinga, G., Mandt, T., Brault, M., Lambert, A. R., Baxter, S. K., Jacoby, K., et al. (2012) · Nature Methods · doi:10.1038/nmeth.2177 · Cited by 99
H. pylori infection alters repair of DNA double-strand breaks via SNHG17
Han, T., Jing, X., Bao, J., Zhao, L., Zhang, A., Miao, R., Guo, H., Zhou, B., Zhang, S., Sun, J., et al. (2020) · Journal of Clinical Investigation · doi:10.1172/jci125581 · Cited by 100
Kinetic analysis of DNA double-strand break repair pathways in Arabidopsis
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Firat, E., Weyerbrock, A., Gaedicke, S., Grosu, A., & Niedermann, G. (2012) · PLoS ONE · doi:10.1371/journal.pone.0047357 · Cited by 101
RAD52 is required for RNA-templated recombination repair in post-mitotic neurons
Welty, S., Teng, Y., Liang, Z., Zhao, W., Sanders, L. H., Greenamyre, J. T., Rubio, M. E., Thathiah, A., Kodali, R. B., Wetzel, R. B., et al. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.808402 · Cited by 104
Comparison of High- and Low-LET Radiation-Induced DNA Double-Strand Break Processing in Living Cells
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Highly active zinc-finger nucleases by extended modular assemblyPreprint
Bhakta, M. S., Henry, I. M., Ousterout, D. G., Das, K. T., Lockwood, S. H., Meckler, J. F., Wallen, M. C., Zykovich, A., Yu, Y., Leo, H., et al. (2012) · Genome Research · doi:10.1101/gr.143693.112 · Cited by 97
MicroRNAs in the DNA Damage/Repair Network and Cancer
Tessitore, A., Cicciarelli, G., Vecchio, F. D., Gaggiano, A., Verzella, D., Fischietti, M., Vecchiotti, D., Capece, D., Zazzeroni, F., & Alesse, E. (2014) · International Journal of Genomics · doi:10.1155/2014/820248 · Cited by 99
Gene therapy for CNS disorders: modalities, delivery and translational challenges
Gao, J., Gunasekar, S., Xia, Z. J., Shalin, K., Jiang, C., Chen, H., Lee, D., Lee, S., Pisal, N. D., Luo, J. N., et al. (2024) · Nature reviews. Neuroscience · doi:10.1038/s41583-024-00829-7 · Cited by 100
Iijima, K., Gatt, A., & Iijima-Ando, K. (2010) · Human Molecular Genetics · doi:10.1093/hmg/ddq200 · Cited by 96
DNA repair in the trinucleotide repeat disorders
Jones, L., Houlden, H., & Tabrizi, S. J. (2016) · The Lancet Neurology · doi:10.1016/s1474-4422(16)30350-7 · Cited by 101
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Ittiprasert, W., Mann, V. H., Karinshak, S. E., Coghlan, A., Rinaldi, G., Sankaranarayanan, G., Chaidee, A., Tanno, T., Kumkhaek, C., Prangtaworn, P., et al. (2019) · eLife · doi:10.7554/elife.41337 · Cited by 96
DNA-PKcs has KU-dependent function in rRNA processing and haematopoiesis
Shao, Z., Flynn, R. A., Crowe, J. L., Zhu, Y., Liang, J., Jiang, W., Aryan, F., Aoude, P., Bertozzi, C. R., Estes, V. M., et al. (2020) · Nature · doi:10.1038/s41586-020-2041-2 · Cited by 95
The balancing act of R-loop biology: The good, the bad, and the ugly
Hegazy, Y. A., Fernando, C. M., & Tran, E. J. (2020) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)49903-0 · Cited by 96
Off-target effects in CRISPR-Cas genome editing for human therapeutics: Progress and challenges
Kalter, N., Fuster‐García, C., Silva, A., Ronco-Díaz, V., Roncelli, S., Turchiano, G., Gorodkin, J., Cathomen, T., Benabdellah, K., Lee, C. M., et al. (2025) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2025.102636 · Cited by 121
Ligase I and ligase III mediate the DNA double-strand break ligation in alternative end-joining
Lu, G., Duan, J., Shu, S., Wang, X., Gao, L., Guo, J., & Zhang, Y. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1521597113 · Cited by 94
Maertens, O., Kuzmickas, R., Manchester, H. E., Emerson, C. E., Gavin, A. G., Guild, C. J., Wong, T. C., De Raedt, T., Bowman-Colin, C., Hatchi, E., et al. (2019) · Cancer Discovery · doi:10.1158/2159-8290.cd-18-0879 · Cited by 95
Zha, S., Jiang, W., Fujiwara, Y., Patel, H., Goff, P. H., Brush, J. W., Dubois, R. L., & Alt, F. W. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1019293108 · Cited by 95
Highly Efficient CRISPR/HDR-Mediated Knock-in for Mouse Embryonic Stem Cells And Zygotes
Wang, B., Li, K., Wang, A., Reiser, M. A., Saunders, T. L., Lockey, R. F., & Wang, J.-W. (2015) · BioTechniques · doi:10.2144/000114339 · Cited by 100
Dual loss of human POLQ and LIG4 abolishes random integration
Saito, S., Maeda, R., & Adachi, N. (2017) · Nature Communications · doi:10.1038/ncomms16112 · Cited by 94
Ahmadi, S. E., Soleymani, M., Shahriyary, F., Amirzargar, M. R., Mahya, O., Fattahi, D., & Safa, M. (2023) · Cancer Gene Therapy · doi:10.1038/s41417-023-00597-z · Cited by 97
Role of recombination activating genes in the generation of antigen receptor diversity and beyond
Nishana, M., & Raghavan, S. C. (2012) · Immunology · doi:10.1111/imm.12009 · Cited by 95
Mitochondria–nucleus network for genome stability
Kaniak, A., & Skoneczna, A. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.01.013 · Cited by 98
DNA Repair Pathways in Trypanosomatids: from DNA Repair to Drug Resistance
Genois, M., Paquet, É. R., Laffitte, M.-C. N., Maity, R., Rodrigue, A., Ouellette, M., & Masson, J. (2014) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00045-13 · Cited by 101
Grabarz, A., Barascu, A., Guirouilh‐Barbat, J., & López, B. S. (2012) · Europe PMC (PubMed Central) · Cited by 93
Off‐target effects of engineered nucleases
Yee, J. (2016) · FEBS Journal · doi:10.1111/febs.13760 · Cited by 95
Preserving genome integrity and function: the DNA damage response and histone modifications
Kim, J. J., Lee, S. Y., & Miller, K. M. (2019) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409238.2019.1620676 · Cited by 96
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Metadata
- Authors
- Lieber, M. R.
- Affiliations
- University of Southern California (US)
- Corresponding author
- Lieber, Michael R.
- ORCID
- Lieber, Michael R.
- Venue
- Annual Review of Biochemistry
- Publisher
- Annual Reviews
- Published
- 2010-06-07
- Volume
- 79
- Issue
- 1
- Pages
- 181-211
- ISSN
- 0066-4154 (ISSN-L)
- 1545-4509
- PMC
- PMC3079308
- OpenAlex
- W2164995160
- Cited by
- 2,882
- References
- 168
- Citations by year
- 2026: 103 · 2025: 144 · 2024: 176 · 2023: 148 · 2022: 199 · 2021: 238 · 2020: 209 · 2019: 187 · 2018: 201 · 2017: 215 · 2016: 212 · 2015: 183 · 2014: 199 · 2013: 168 · 2012: 148
- FWCI
- 13.03
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Annual Review of Biochemistry (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Cancer Institute (R01CA100504)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Effects of Radiation Exposure
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › CRISPR and Genetic Engineering
- Keywords
- DNA double-strand break repair, non-homologous end joining, homologous recombination, DNA ligase IV, DNA polymerase IV, chromosomal translocation, V(D)J recombination, class switch recombination, immunodeficiency, radiosensitivity
- MeSH terms
- Animals, Deoxyribonucleases, DNA-Directed DNA Polymerase, DNA Repair, Humans, DNA Ligases, DNA Breaks, Double-Stranded
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