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Regulation of Homologous Recombination in Eukaryotes
Open accessAbstract
Homologous recombination (HR) is required for accurate chromosome segregation during the first meiotic division and constitutes a key repair and tolerance pathway for complex DNA damage, including DNA double-strand breaks, interstrand crosslinks, and DNA gaps. In addition, recombination and replication are inextricably linked, as recombination recovers stalled and broken replication forks, enabling the evolution of larger genomes/replicons. Defects in recombination lead to genomic instability and elevated cancer predisposition, demonstrating a clear cellular need for recombination. However, recombination can also lead to genome rearrangements. Unrestrained recombination causes undesired endpoints (translocation, deletion, inversion) and the accumulation of toxic recombination intermediates. Evidently, HR must be carefully regulated to match specific cellular needs. Here, we review the factors and mechanistic stages of recombination that are subject to regulation and suggest that recombination achieves flexibility and robustness by proceeding through metastable, reversible intermediates.
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“because it is only readily available in dividing cells [110,111]”
From CRISPR-Cas: Converting A Bacterial Defence Mechanism into A State-of-the-Art Genetic Manipulation Tool (2019) · cites this paper as [110]
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“Cell cycle phase dominates the choice between NHEJ and HDR, with HDR taking place mainly in S and G2 phases due to the availability of sister chromatids as templates.61”
From CRISPR-Cas9: a new and promising player in gene therapy (2015) · cites this paper as [61]
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Cites
Genome maintenance mechanisms for preventing cancer
Hoeijmakers, J. H. J. (2001) · Nature · doi:10.1038/35077232 · Cited by 3,939
Multiple Pathways of Recombination Induced by Double-Strand Breaks in Saccharomyces cerevisiae
Pâques, F., & Haber, J. E. (1999) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.63.2.349-404.1999 · Cited by 2,120
Drake, J. W., Charlesworth, B., Charlesworth, D., & Crow, J. F. (1998) · Genetics · doi:10.1093/genetics/148.4.1667 · Cited by 1,932
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
Human CtIP promotes DNA end resection
Sartori, A. A., Lukas, C., Coates, J., Mistrik, M., Fu, S., Bartek, J., Baer, R., Lukas, J., & Jackson, S. P. (2007) · Nature · doi:10.1038/nature06337 · Cited by 1,362
Mammalian cyclin-dependent kinases
Malumbres, M., & Barbacid, M. (2005) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2005.09.005 · Cited by 1,333
Regulation of DNA double-strand break repair pathway choice
Shrivastav, M., De Haro, L. P., & Nickoloff, J. A. (2008) · Cell Research · doi:10.1038/cr.2007.111 · Cited by 1,329
Regulation of DNA repair throughout the cell cycle
Branzei, D., & Foiani, M. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2351 · Cited by 1,228
Homologous recombination in DNA repair and DNA damage tolerance
Li, X., & Heyer, W. (2008) · Cell Research · doi:10.1038/cr.2008.1 · Cited by 1,203
Self-citationSgs1 Helicase and Two Nucleases Dna2 and Exo1 Resect DNA Double-Strand Break Ends
Zhu, Z., Chung, W.-H., Shim, E. Y., Lee, S. E., & Ira, G. (2008) · Cell · doi:10.1016/j.cell.2008.08.037 · Cited by 1,108
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Seeger, T., Porteus, M. H., & Wu, J. C. (2017) · Circulation Research · doi:10.1161/circresaha.116.310197 · Cited by 48
Schouten, P. C., Marmé, F., Aulmann, S., Sinn, H., Essen, H. F. H. V., Ylstra, B., Hauptmann, M., Schneeweiß, A., & Linn, S. C. (2014) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-14-1894 · Cited by 47
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Hung, S. S. C., McCaughey, T., Swann, O. G., Pébay, A., & Hewitt, A. W. (2016) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2016.05.001 · Cited by 49
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Li, J., & Xu, X. (2016) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmw045 · Cited by 53
New advances in CRISPR/Cas-mediated precise gene-editing techniques
Richardson, C., Kelsh, R. N., & Richardson, R. J. (2023) · Disease Models & Mechanisms · doi:10.1242/dmm.049874 · Cited by 48
Godin, S. K., Meslin, C., Kabbinavar, F. F., Bratton-Palmer, D. S., Hornack, C., Mihalevic, M. J., Yoshida, K., Sullivan, M. R., Clark, N. L., & Bernstein, K. A. (2015) · Genetics · doi:10.1534/genetics.114.173518 · Cited by 44
Oh, S., Wang, Y., Zimbric, J., & Hendrickson, E. A. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks1326 · Cited by 46
Amann, T., Schmieder, V., Faustrup Kildegaard, H., Borth, N., & Andersen, M. R. (2019) · Biotechnology and Bioengineering · doi:10.1002/bit.27101 · Cited by 46
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Ambjørn, S. M., Duxin, J. P., Hertz, E. P. T., Nasa, I., Duro, J., Kruse, T., Mendez, B. L., Rymarczyk, B., Cressey, L. E., Hansen, T. V. O., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-26079-0 · Cited by 49
Effects of XRCC2 and RAD51B mutations on somatic and meiotic recombination in A rabidopsis thaliana
Ines, O. D., Degroote, F., Amiard, S., Goubely, C., Gallego, M. E., & White, C. I. (2013) · The Plant Journal · doi:10.1111/tpj.12182 · Cited by 45
Rad51 presynaptic filament stabilization function of the mouse Swi5–Sfr1 heterodimeric complex
Tsai, S.-P., Su, G.-C., Lin, S., Chung, C.-I., Xue, X., Dunlop, M. H., Akamatsu, Y., Jasin, M., Sung, P., & Chi, P. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks305 · Cited by 42
Contributions of the RAD51 N-terminal domain to BRCA2-RAD51 interaction
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Krijger, P. H. L., van den Berk, P. C. M., Wit, N., Langerak, P., Jansen, J. G., Reynaud, C., de Wind, N., & Jacobs, H. (2011) · DNA repair · doi:10.1016/j.dnarep.2011.08.005 · Cited by 50
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Wilkinson, R. A., & Wiedenheft, B. (2014) · F1000Prime Reports · doi:10.12703/p6-3 · Cited by 46
Lee, K. Y., Im, J., Shibata, E., & Dutta, A. (2017) · Molecular Cell · doi:10.1016/j.molcel.2017.08.021 · Cited by 46
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Chen, H., He, C., Wang, C., Wang, X., Ruan, F., Yan, J., Yin, P., Wang, Y., & Yan, S. (2021) · The Plant Cell · doi:10.1093/plcell/koab136 · Cited by 49
Fijen, C., & Rothenberg, E. (2021) · DNA repair · doi:10.1016/j.dnarep.2021.103170 · Cited by 43
A quantitative model of the major pathways for radiation-induced DNA double-strand break repair
Belov, O., Krasavin, E. A., Lyashko, M. S., Batmunkh, M., & Sweilam, N. H. (2014) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2014.09.024 · Cited by 45
Miranda, A., Gomez-Varela, A. I., Stylianou, A., Hirvonen, L. M., Sánchez, H., & Beule, P. D. (2020) · Nanoscale · doi:10.1039/d0nr07203f · Cited by 46
Targeted gene therapies: tools, applications, optimization
Humbert, O., Davis, L., & Maizels, N. (2012) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.3109/10409238.2012.658112 · Cited by 45
Liu, Z., Hui, Y., Shi, L., Chen, Z., Xu, X., Chi, L., Fan, B., Fang, Y., Liu, Y., Ma, L., et al. (2016) · Stem Cell Reports · doi:10.1016/j.stemcr.2016.07.021 · Cited by 43
Amendola, P. G., Zaghet, N., Ramalho, J. J., Johansen, J. V., Boxem, M., & Salcini, A. E. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1006632 · Cited by 44
Tullio, L. D., Kaniecki, K., Kwon, Y., Crickard, J. B., Sung, P., & Greene, E. C. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.09.073 · Cited by 43
CRISPR/Cas Applications in Myotonic Dystrophy: Expanding Opportunities
Raaijmakers, R. H. L., Ripken, L., Ausems, C. R. M., & Wansink, D. G. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20153689 · Cited by 46
Peterson, D., Barone, P., Lenderts, B., Schwartz, C. S., Feigenbutz, L., Clair, G. S., Jones, S., & Svitashev, S. K. (2021) · Plant Biotechnology Journal · doi:10.1111/pbi.13613 · Cited by 45
Meiotic DNA joint molecule resolution depends on Nse5-Nse6 of the Smc5-Smc6 holocomplex
Wehrkamp‐Richter, S., Hyppa, R. W., Prudden, J., Smith, G. R., & Boddy, M. N. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks713 · Cited by 43
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Strzałka, W., Zgłobicki, P., Kowalska, E., Bażant, A., Dziga, D., & Banaś, A. K. (2020) · Genes · doi:10.3390/genes11121450 · Cited by 48
Singh, S., Chaudhary, R., Deshmukh, R. K., & Tiwari, S. (2022) · Plant Molecular Biology · doi:10.1007/s11103-022-01321-5 · Cited by 42
Onishi‐Seebacher, M., & Korbel, J. O. (2011) · BioEssays · doi:10.1002/bies.201100075 · Cited by 43
Naccarati, A., Rosa, F., Vymetalkova, V. P., Barone, E., Jirásková, K., Gaetano, C. D., Novotný, J., Levý, M., Vodičková, Ľ., Gemignani, F., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.6804 · Cited by 42
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Ingram, S., Warmenhoven, J.-W., Henthorn, N. T., Smith, E., Chadwick, A. L., Burnet, N. G., Mackay, R. I., Kirkby, N. F., Kirkby, K. J., & Merchant, M. J. (2019) · Scientific Reports · doi:10.1038/s41598-019-42901-8 · Cited by 42
EXO1 resection at G-quadruplex structures facilitates resolution and replication
Stroik, S., Kurtz, K., Lin, K. C., Karachenets, S., Myers, C. L., Bielinsky, A., & Hendrickson, E. A. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa199 · Cited by 42
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Lan, W.-H., Lin, S.-Y., Kao, C.-Y., Chang, W.-H., Yeh, H., Chang, H.-Y., Chi, P., & Li, H. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1920368117 · Cited by 40
Banerjee, S., & Roy, S. (2021) · Cell Cycle · doi:10.1080/15384101.2021.1966584 · Cited by 40
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Kumar, R., & Cheok, C. F. (2014) · DNA repair · doi:10.1016/j.dnarep.2013.12.004 · Cited by 45
Schröpfer, S., Kobbe, D., Hartung, F., Knoll, A., & Puchta, H. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt1004 · Cited by 41
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Gómez-Cabello, D., Jimeno, S., Fernández-Ávila, M. J., & Huertas, P. (2013) · PLoS ONE · doi:10.1371/journal.pone.0077206 · Cited by 40
Haloferax volcanii —a model archaeon for studying DNA replication and repair
Pérez-Arnaiz, P., Dattani, A., Smith, V., & Allers, T. (2020) · Open Biology · doi:10.1098/rsob.200293 · Cited by 46
CRISPR-based strategies for targeted transgene knock-in and gene correction
Lau, C., Tin, C., & Suh, Y. (2020) · Faculty Reviews · doi:10.12703/r/9-20 · Cited by 46
Haider, S., & Mussolino, C. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26094067 · Cited by 45
Alariqi, M., Ramadan, M., Yu, L., Hui, F., Hussain, A., Zhou, X., Yu, Y., Zhang, X., & Jin, S. (2025) · Advanced Science · doi:10.1002/advs.202416331 · Cited by 42
Domenico, E. G. D., Romano, E., Porto, P. D., & Ascenzioni, F. (2014) · BioMed Research International · doi:10.1155/2014/787404 · Cited by 39
Xue, C., Daley, J. M., Xue, X., Steinfeld, J. B., Kwon, Y., Sung, P., & Greene, E. C. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz810 · Cited by 40
Peritore, M., Reußwig, K.-U., Bantele, S. C. S., Straub, T., & Pfander, B. (2021) · Molecular Cell · doi:10.1016/j.molcel.2021.02.005 · Cited by 44
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Vu, G. T. H., Cao, H. X., Fauser, F., Reiss, B., Puchta, H., & Schubert, I. A. (2017) · The Plant Journal · doi:10.1111/tpj.13634 · Cited by 39
Swi5–Sfr1 stimulates Rad51 recombinase filament assembly by modulating Rad51 dissociation
Lu, C., Yeh, H., Su, G.-C., Ito, K., Kurokawa, Y., Iwasaki, H., Chi, P., & Li, H. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1812753115 · Cited by 39
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Zhou, J., Zhou, X. A., Zhang, N., & Wang, J. (2020) · Cancer Biology and Medicine · doi:10.20892/j.issn.2095-3941.2020.0177 · Cited by 40
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Liu, T., & Huang, J. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1649-5 · Cited by 39
Machida, S., Takaku, M., Ikura, M., Sun, J., Suzuki, H., Kobayashi, W., Kinomura, A., Osakabe, A., Tachiwana, H., Horikoshi, Y., et al. (2014) · Scientific Reports · doi:10.1038/srep04863 · Cited by 38
Shinohara, M., Hayashihara, K., Grubb, J., Bishop, D. K., & Shinohara, A. (2015) · Journal of Cell Science · doi:10.1242/jcs.161554 · Cited by 38
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Li, P., Zhang, L., Li, Z., Xu, C., Du, X., & Wu, S. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03396-8 · Cited by 38
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Felgentreff, K., Du, L., Weinacht, K. G., Dobbs, K., Bartish, M., Giliani, S., Schlaeger, T. M., DeVine, A. L., Schambach, A., Woodbine, L. J., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1323649111 · Cited by 37
The USP1-UAF1 complex interacts with RAD51AP1 to promote homologous recombination repair
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Jo, Y.-I., Suresh, B., Kim, S., & Ramakrishna, S. (2015) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2015.09.003 · Cited by 36
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Qi, Z., & Greene, E. C. (2016) · Methods · doi:10.1016/j.ymeth.2016.03.027 · Cited by 38
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Kwon, Y., Abe, K., Endo, M., Osakabe, K., Ohtsuki, N., Nishizawa‐Yokoi, A., Tagiri, A., Saika, H., & Toki, S. (2013) · BMC Plant Biology · doi:10.1186/1471-2229-13-62 · Cited by 35
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Luo, S., Yeh, H., Lan, W.-H., Wu, Y., Yang, C., Chang, H.-Y., Su, G.-C., Lee, C., Wu, W., Li, H., et al. (2021) · Nature Communications · doi:10.1038/s41467-020-20258-1 · Cited by 34
Homologous Recombination in Eukaryotes
Amunugama, R., & Fishel, R. A. (2012) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-387665-2.00007-9 · Cited by 39
Enhancement of ADP release from the RAD51 presynaptic filament by the SWI5-SFR1 complex
Su, G.-C., Chung, C.-I., Liao, C.-Y., Lin, S., Tsai, C. S., Huang, T., Li, H., & Chi, P. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt879 · Cited by 35
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Metadata
- Authors
- Heyer, W.-D., Ehmsen, K. T., & Liu, J.
- Affiliations
- University of California, Davis (US)
- Venue
- Annual Review of Genetics
- Publisher
- Annual Reviews
- Published
- 2010-12-01
- Volume
- 44
- Issue
- 1
- Pages
- 113-139
- ISSN
- 0066-4197 (ISSN-L)
- 1545-2948
- PMC
- PMC4114321
- OpenAlex
- W2109879947
- Cited by
- 1,066
- References
- 177
- Citations by year
- 2026: 26 · 2025: 44 · 2024: 54 · 2023: 64 · 2022: 70 · 2021: 91 · 2020: 86 · 2019: 75 · 2018: 79 · 2017: 86 · 2016: 83 · 2015: 71 · 2014: 67 · 2013: 67 · 2012: 62
- FWCI
- 4.67
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Annual Review of Genetics (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Tobacco-Related Disease Research Program
- National Institutes of Health
- National Cancer Institute (CA92776, R01CA092276, R03CA092776)
- National Institute of General Medical Sciences (GM58015, R01GM058015)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Keywords
- homologous recombination, recombination regulation, DNA double-strand breaks, meiotic chromosome segregation, DNA repair, DNA damage tolerance, replication fork recovery, genomic instability, cancer susceptibility, genome rearrangement, translocation, recombination intermediates, metastable intermediates, eukaryotic cells
- MeSH terms
- Animals, DNA Repair, Humans, Recombination, Genetic, Yeasts
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