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Reassembly of shattered chromosomes in Deinococcus radiodurans
Abstract
Dehydration or desiccation is one of the most frequent and severe challenges to living cells. The bacterium Deinococcus radiodurans is the best known extremophile among the few organisms that can survive extremely high exposures to desiccation and ionizing radiation, which shatter its genome into hundreds of short DNA fragments. Remarkably, these fragments are readily reassembled into a functional 3.28-megabase genome. Here we describe the relevant two-stage DNA repair process, which involves a previously unknown molecular mechanism for fragment reassembly called 'extended synthesis-dependent strand annealing' (ESDSA), followed and completed by crossovers. At least two genome copies and random DNA breakage are requirements for effective ESDSA. In ESDSA, chromosomal fragments with overlapping homologies are used both as primers and as templates for massive synthesis of complementary single strands, as occurs in a single-round multiplex polymerase chain reaction. This synthesis depends on DNA polymerase I and incorporates more nucleotides than does normal replication in intact cells. Newly synthesized complementary single-stranded extensions become 'sticky ends' that anneal with high precision, joining together contiguous DNA fragments into long, linear, double-stranded intermediates. These intermediates require RecA-dependent crossovers to mature into circular chromosomes that comprise double-stranded patchworks of numerous DNA blocks synthesized before radiation, connected by DNA blocks synthesized after radiation.
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“Moreover, previous study showed that bacterium Deinococcus radiodurans can repair its genome form hundreds of short DNA fragments resulting from exogenous damages.”
From CRISPR-Cas9: a new and promising player in gene therapy (2015) · cites this paper as [65]
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Cites
Genome Sequence of the Radioresistant Bacterium Deinococcus radiodurans R1
White, O. R., Eisen, J. A., Heidelberg, J. F., Hickey, E. K., Peterson, J. D., Dodson, R. J., Haft, D. H., Gwinn, M. L., Nelson, W. C., Richardson, D. L., et al. (1999) · Science · doi:10.1126/science.286.5444.1571 · Cited by 949
Lindahl, T. L. (1982) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.51.070182.000425 · Cited by 904
Deinococcus radiodurans — the consummate survivor
Cox, M. M., & Battista, J. R. (2005) · Nature Reviews Microbiology · doi:10.1038/nrmicro1264 · Cited by 735
Makarova, K. S., Aravind, L., Wolf, Y. I., Tatusov, R. L., Minton, K. W., Koonin, E. V., & Daly, M. J. (2001) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.65.1.44-79.2001 · Cited by 733
Rayssiguier, C., Thaler, D. S., & Radman, M. (1989) · Nature · doi:10.1038/342396a0 · Cited by 715
Self-citationMattimore, V, & Battista, J. R. (1996) · Journal of Bacteriology · doi:10.1128/jb.178.3.633-637.1996 · Cited by 687
Anderson, A. W. (1956) · Food technology · Cited by 400
Rainey, F. A., Keren, R., Ferreira, M. S., Gatz, B. Z., Nobre, M. F., Bagaley, D. R., Rash, B. A., Park, M., Earl, A. M., Shank, N. C., et al. (2005) · Applied and Environmental Microbiology · doi:10.1128/aem.71.9.5225-5235.2005 · Cited by 360
DNA repair in the extremely radioresistant bacterium Deinococcus radiodurans
Minton, K. W. (1994) · Molecular Microbiology · doi:10.1111/j.1365-2958.1994.tb00397.x · Cited by 292
Why is Deinococcus radiodurans so resistant to ionizing radiation?
Battista, J. R., Earl, A. M., & Park, M.-J. (1999) · Trends in Microbiology · doi:10.1016/s0966-842x(99)01566-8 · Cited by 257
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Items 101–200 of 445
Scientific Opinion on the efficacy and microbiological safety of irradiation of food
(BIOHAZ), E. P. O. B. H. (2011) · EFSA Journal · doi:10.2903/j.efsa.2011.2103 · Cited by 52
DNA recognition and the precleavage state during single‐stranded DNA transposition in D. radiodurans
Hickman, A. B., James, J. A., Barábas, O., Pasternak, C., Ton‐Hoang, B., Chandler, M., Sommer, S., & Dyda, F. (2010) · The EMBO Journal · doi:10.1038/emboj.2010.241 · Cited by 51
Self-citationde la Tour, C. B., Boisnard, S., Norais, C. A., Toueille, M., Bentchikou, E., Vannier, F., Cox, M. M., Sommer, S., & Servant, P. (2011) · DNA repair · doi:10.1016/j.dnarep.2011.09.010 · Cited by 51
Self-citationBentchikou, E., Servant, P., Coste, G., & Sommer, S. (2007) · Journal of Bacteriology · doi:10.1128/jb.00452-07 · Cited by 51
Self-citationGeorge, N. P., Ngo, K. V., Chitteni‐Pattu, S., Norais, C. A., Battista, J. R., Cox, M. M., & Keck, J. L. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.367573 · Cited by 50
Recombinational branch migration by the RadA/Sms paralog of RecA in Escherichia coli
Cooper, D. L., & Lovett, S. T. (2016) · eLife · doi:10.7554/elife.10807 · Cited by 50
Rajpurohit, Y. S., Bihani, S. C., Waldor, M. K., & Misra, H. S. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.736389 · Cited by 49
RecO Is Essential for DNA Damage Repair in Deinococcus radiodurans
Xu, G., Wang, L., Chen, H., Lu, H., Ying, N., Tian, B., & Hua, Y. (2008) · Journal of Bacteriology · doi:10.1128/jb.01851-07 · Cited by 48
The structure of DdrB from Deinococcus: a new fold for single-stranded DNA binding proteins
Sugiman‐Marangos, S. N., & Junop, M. S. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq036 · Cited by 47
DNA Replication and Genomic Architecture of Very Large Bacteria
Angert, E. R. (2010) · Annual Review of Microbiology · doi:10.1146/annurev-micro-090110-102827 · Cited by 47
Ruiz‐González, M. X., Czirják, G. Á., Genevaux, P., Møller, A. P., Mousseau, T. A., & Heeb, P. (2016) · Scientific Reports · doi:10.1038/srep22969 · Cited by 46
Recent progress in understanding the molecular mechanisms of radioresistance in Deinococcus bacteria
Munteanu, A. C., Uivaroşi, V., & Andries, A. A. (2015) · Extremophiles · doi:10.1007/s00792-015-0759-9 · Cited by 47
Kota, S., Charaka, V., Ringgaard, S., Waldor, M. K., & Misra, H. S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0085288 · Cited by 46
Dulermo, R., Onodera, T., Coste, G., Passot, F. M., Dutertre, M., Porteron, M., Confalonieri, F., Sommer, S., & Pasternak, C. (2015) · PLoS ONE · doi:10.1371/journal.pone.0124358 · Cited by 45
Self-citationAuthority, E. F. S. (2011) · EFSA Journal · doi:10.2903/j.efsa.2011.2107 · Cited by 45
Westmoreland, J., Ma, W., Yan, Y., Hulle, K. V., Malkova, A., & Resnick, M. A. (2009) · PLoS Genetics · doi:10.1371/journal.pgen.1000656 · Cited by 44
Bauermeister, A., Bentchikou, E., Moeller, R., & Rettberg, P. (2009) · Archives of Microbiology · doi:10.1007/s00203-009-0522-7 · Cited by 44
RecombinantD. radioduranscells for bioremediation of heavy metals from acidic/neutral aqueous wastes
Misra, C. S., Appukuttan, D., Kantamreddi, V. S. S., Rao, A. S., & Apte, S. K. (2012) · Bioengineered · doi:10.4161/bbug.3.1.18878 · Cited by 44
de la Tour, C. B., Passot, F. M., Toueille, M., Mirabella, B., Guerin, P. J., Blanchard, L., Servant, P., de Groot, A., Sommer, S., & Armengaud, J. (2013) · PROTEOMICS · doi:10.1002/pmic.201300249 · Cited by 43
Self-citationEvolutionary consequences of polyploidy in prokaryotes and the origin of mitosis and meiosis
Markov, A. V., & Kaznacheev, I. S. (2016) · Biology Direct · doi:10.1186/s13062-016-0131-8 · Cited by 44
Rivasseau, C., Farhi, E., Compagnon, E., Cyr, D. D. G. S., van Lis, R., Falconet, D., Kuntz, M., Atteia, A., & Couté, A. (2016) · Journal of Phycology · doi:10.1111/jpy.12442 · Cited by 43
Maurya, G. K., Modi, K., Banerjee, M., Chaudhary, R., Rajpurohit, Y. S., & Misra, H. (2018) · Msphere · doi:10.1128/msphere.00325-18 · Cited by 43
Polyploidy in halophilic archaea: regulation, evolutionary advantages, and gene conversion
Ludt, K., & Soppa, J. (2019) · Biochemical Society Transactions · doi:10.1042/bst20190256 · Cited by 40
Lu, H., Chen, H., Xu, G., Shah, A. M.-U.-H., & Hua, Y. (2011) · DNA repair · doi:10.1016/j.dnarep.2011.10.013 · Cited by 40
Devigne, A., Mersaoui, S. Y., de la Tour, C. B., Sommer, S., & Servant, P. (2013) · DNA repair · doi:10.1016/j.dnarep.2013.01.004 · Cited by 40
Self-citationSeed longevity and genome damage
Waterworth, W. M., Balobaid, A., & West, C. (2024) · Bioscience Reports · doi:10.1042/bsr20230809 · Cited by 40
Recombinational DNA repair in a cellular context: a search for the homology search
Weiner, A., Zauberman, N., & Minsky, A. (2009) · Nature Reviews Microbiology · doi:10.1038/nrmicro2206 · Cited by 41
The Roles of Bacterial DNA Double-Strand Break Repair Proteins in Chromosomal DNA Replication
Sinha, A. K., Possoz, C., & Leach, D. R. F. (2020) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuaa009 · Cited by 38
Horizontal Gene Transfer in Metal and Radionuclide Contaminated Soils
Sobecky, P. A., & Coombs, J. M. (2009) · Methods in molecular biology · doi:10.1007/978-1-60327-853-9_26 · Cited by 40
A comparative proteomic approach to better define Deinococcus nucleoid specificities
Toueille, M., Mirabella, B., Guerin, P. J., de la Tour, C. B., Boisnard, S., Nguyen, H. H., Blanchard, L., Servant, P., de Groot, A., Sommer, S., et al. (2012) · Journal of Proteomics · doi:10.1016/j.jprot.2012.03.002 · Cited by 37
Self-citationvon Kügelgen, A., van Dorst, S., Yamashita, K., Sexton, D. L., Tocheva, E. I., Murshudov, G., Alva, V., & Bharat, T. A. M. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2215808120 · Cited by 35
Agapov, A., & Kulbachinskiy, A. V. (2015) · Biochemistry (Moscow) · doi:10.1134/s0006297915100016 · Cited by 36
Nakane, S., Nakagawa, N., Kuramitsu, S., & Masui, R. (2009) · Nucleic Acids Research · doi:10.1093/nar/gkp064 · Cited by 35
RecA protein assures fidelity of DNA repair and genome stability in Deinococcus radiodurans
Repar, J., Cvjetan, S., Slade, D., Radman, M., Zahradka, D., & Zahradka, K. (2010) · DNA repair · doi:10.1016/j.dnarep.2010.08.003 · Cited by 35
Self-citationOtt, E., Kawaguchi, Y., Gutmann-Özgen, N., Yamagishi, A., Rabbow, E., Rettberg, P., Weckwerth, W., & Milojević, T. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.00909 · Cited by 35
Blanchard, L., & de Groot, A. (2021) · Cells · doi:10.3390/cells10040924 · Cited by 35
Kish, A., & DiRuggiero, J. (2008) · Journal of Bacteriology · doi:10.1128/jb.00292-08 · Cited by 35
Towards understanding the extreme radiation resistance of Ustilago maydis
Holloman, W. K., Schirawski, J., & Holliday, R. (2007) · Trends in Microbiology · doi:10.1016/j.tim.2007.10.007 · Cited by 33
Preferential D-loop extension by a translesion DNA polymerase underlies error-prone recombination
Pomerantz, R. T., Kurth, I., Goodman, M. F., & O’Donnell, M. E. (2013) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.2573 · Cited by 33
Hsu, H.-F., Ngo, K. V., Chitteni‐Pattu, S., Cox, M. M., & Li, H. (2011) · Biochemistry · doi:10.1021/bi200423t · Cited by 33
Extreme Views on Prokaryote Evolution
Dion, P. (2007) · Soil biology · doi:10.1007/978-3-540-74231-9_3 · Cited by 35
Servant, P., Jolivet, E., Bentchikou, E., Mennecier, S., Bailone, A., & Sommer, S. (2007) · Molecular Microbiology · doi:10.1111/j.1365-2958.2007.06003.x · Cited by 36
Self-citationIdentification of a DNA processing complex from Deinococcus radiodurans
Kota, S., & Misra, H. S. (2008) · Biochemistry and Cell Biology · doi:10.1139/o08-122 · Cited by 33
Shuryak, I., & Brenner, D. J. (2009) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2009.08.003 · Cited by 32
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Caiola, M., & Billi, D. (2007) · Cellular origin and life in extreme habitats · doi:10.1007/978-1-4020-6112-7_30 · Cited by 29
Lovett, S. T. (2006) · Nature · doi:10.1038/443517b · Cited by 32
From Target Identification to Drug Development in Space: Using the Microgravity Assist
Braddock, M. (2019) · Current Drug Discovery Technologies · doi:10.2174/1570163816666190112150014 · Cited by 31
Ithurbide, S., Coste, G., Lisboa, J., Eugénie, N., Bentchikou, E., de la Tour, C. B., Liger, D., Confalonieri, F., Sommer, S., Quevillon‐Chéruel, S., et al. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.01253 · Cited by 31
Self-citationDesai, S. S., Rajpurohit, Y. S., Misra, H. S., & Deobagkar, D. N. (2011) · Microbiology · doi:10.1099/mic.0.049361-0 · Cited by 31
Khairnar, N. P., Kamble, V. A., Mangoli, S. H., Apte, S. K., & Misra, H. S. (2007) · Molecular Microbiology · doi:10.1111/j.1365-2958.2007.05779.x · Cited by 31
The Family X DNA Polymerase from Deinococcus radiodurans Adopts a Non-standard Extended Conformation
Leulliot, N., Cladière, L., Lecointe, F., Christiane, D. D., Hübscher, U., & TILBEURGH, H. V. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m809342200 · Cited by 30
Blasius, M., Buob, R., Shevelev, I. V., & Hübscher, U. (2007) · BMC Molecular Biology · doi:10.1186/1471-2199-8-69 · Cited by 30
Szydlowski, L. M., Bulbul, A. A., Simpson, A. C., Kaya, D. E., Singh, N. K., Sezerman, U. O., Łabaj, P. P., Kosciolek, T., & Venkateswaran, K. (2024) · Microbiome · doi:10.1186/s40168-024-01916-8 · Cited by 31
Ngo, K. V., Molzberger, E. T., Chitteni‐Pattu, S., & Cox, M. M. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.459230 · Cited by 29
Kriško, A., Smole, Z., Debret, G., Nikolić, N., & Radman, M. (2010) · Journal of Molecular Biology · doi:10.1016/j.jmb.2010.08.012 · Cited by 29
Self-citationThe Essential Role of the Deinococcus radiodurans ssb Gene in Cell Survival and Radiation Tolerance
Lockhart, J. S., & DeVeaux, L. C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0071651 · Cited by 29
Effect of a recD Mutation on DNA Damage Resistance and Transformation in Deinococcus radiodurans
Servinsky, M. D., & Julin, D. A. (2007) · Journal of Bacteriology · doi:10.1128/jb.00409-07 · Cited by 29
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Li, M., Sun, H., Feng, Q., Lu, H., Zhao, Y., Zhang, H., Xu, X., Jiao, J., Wang, L., & Hua, Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0054420 · Cited by 28
Experimental evolution of extremophile resistance to ionizing radiation
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Doninck, K. V., Mandigo, M., Hur, J. H., Wang, P., Guglielmini, J., Milinkovitch, M. C., Lane, W. S., & Meselson, M. S. (2009) · PLoS Genetics · doi:10.1371/journal.pgen.1000401 · Cited by 28
Gutsche, I., Vujičić‐Žagar, A., Siebert, X., Servant, P., Vannier, F., Castaing, B., Gallet, B., Heulin, T., de Groot, A., Sommer, S., et al. (2008) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2008.03.009 · Cited by 28
Self-citationKota, S., Charaka, V., & Misra, H. S. (2014) · Journal of Genetics · doi:10.1007/s12041-014-0382-z · Cited by 27
Ithurbide, S., Bentchikou, E., Coste, G., Bost, B., Servant, P., & Sommer, S. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005636 · Cited by 27
Self-citationAwile, O., Kriško, A., Sbalzarini, I. F., & Žagrović, B. (2010) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000854 · Cited by 27
Ohba, H., Satoh, K., Sghaier, H., Yanagisawa, T., & Narumi, I. (2009) · Extremophiles · doi:10.1007/s00792-009-0232-8 · Cited by 27
Khairnar, N. P., & Misra, H. S. (2009) · Microbiology · doi:10.1099/mic.0.029223-0 · Cited by 27
Tarazona, E., Lucas‐Lledó, J. I., Carmona, M. J., & García-Roger, E. M. (2020) · Scientific Reports · doi:10.1038/s41598-020-77727-2 · Cited by 26
Basu, B. (2022) · Current Research in Microbial Sciences · doi:10.1016/j.crmicr.2022.100153 · Cited by 26
Sadowska‐Bartosz, I., & Bartosz, G. (2023) · International Journal of Radiation Biology · doi:10.1080/09553002.2023.2241895 · Cited by 28
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Horikawa, D. D. (2008) · Biological Sciences in Space · doi:10.2187/bss.22.93 · Cited by 26
Meyer, L., Coste, G., Sommer, S., Oberto, J., Confalonieri, F., Servant, P., & Pasternak, C. (2018) · Journal of Bacteriology · doi:10.1128/jb.00129-18 · Cited by 26
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Gene regulation for the extreme resistance to ionizing radiation of Deinococcus radiodurans.
Wang, W.-Z., Ma, Y., He, J.-Y., Qi, H.-Z., Xiao, F.-Z., & He, S.-Y. (2019) · Gene · doi:10.1016/j.gene.2019.144008 · Cited by 23
Eugénie, N., Zivanovic, Y., Lelandais, G., Coste, G., de la Tour, C. B., Bentchikou, E., Servant, P., & Confalonieri, F. (2021) · Cells · doi:10.3390/cells10102536 · Cited by 25
Tapias, A., Leplat, C., & Confalonieri, F. (2009) · Extremophiles · doi:10.1007/s00792-008-0221-3 · Cited by 25
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Peeples, T. L. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-800021-2.00010-8 · Cited by 25
Mishra, S., Chaudhary, R., Singh, S. K., Kota, S., & Misra, H. S. (2019) · Journal of Bacteriology · doi:10.1128/jb.00154-19 · Cited by 25
Ujaoney, A. K., Potnis, A. A., Kane, P., Mukhopadhyaya, R., & Apte, S. K. (2010) · Journal of Bacteriology · doi:10.1128/jb.00752-10 · Cited by 25
Daly, M. J. (2023) · Canadian Journal of Microbiology · doi:10.1139/cjm-2023-0059 · Cited by 24
Devigne, A., Guerin, P. J., Lisboa, J., Quevillon‐Chéruel, S., Armengaud, J., Sommer, S., de la Tour, C. B., & Servant, P. (2016) · mSphere · doi:10.1128/msphere.00036-15 · Cited by 24
Self-citationPiechura, J. R., Tseng, T.-L., Hsu, H.-F., Byrne, R. T., Windgassen, T. A., Chitteni‐Pattu, S., Battista, J. R., Li, H., & Cox, M. M. (2014) · DNA repair · doi:10.1016/j.dnarep.2014.12.001 · Cited by 24
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Adam‐Guillermin, C., Hertel‐Aas, T., Oughton, D. H., Blanchard, L., Alonzo, F., Armant, O., & Horemans, N. (2018) · Annals of the ICRP · doi:10.1177/0146645318756844 · Cited by 24
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Zhang, H., Xu, Q., Lu, M., Xu, X., Wang, Y., Wang, L., Zhao, Y., & Hua, Y. (2014) · DNA repair · doi:10.1016/j.dnarep.2014.04.012 · Cited by 23
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Cao, Z., Mueller, C. W., & Julin, D. A. (2009) · DNA repair · doi:10.1016/j.dnarep.2009.10.009 · Cited by 22
Kamble, V. A., Rajpurohit, Y. S., Srivastava, A. K., & Misra, H. S. (2009) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2009.01855.x · Cited by 23
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Zhou, Q., Zhang, X., Xu, H., Xu, B., & Hua, Y. (2007) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2007.00703.x · Cited by 23
Rajpurohit, Y. S., Sharma, D. K., & Misra, H. S. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.636178 · Cited by 22
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Passot, F. M., Nguyen, H. H., Dard-Dascot, C., Thermes, C., Servant, P., Espéli, O., & Sommer, S. (2015) · Molecular Microbiology · doi:10.1111/mmi.13064 · Cited by 22
Self-citationTopoisomerase IB of Deinococcus radiodurans resolves guanine quadruplex DNA structures in vitro
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Misra, C. S., Mukhopadhyaya, R., & Apte, S. K. (2014) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2014.09.013 · Cited by 21
Ionizing Radiation-induced Proteomic Oxidation in Escherichia coli
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Sghaier, H., Narumi, I., Satoh, K., Ohba, H., & Mitomo, H. (2007) · Theory in Biosciences · doi:10.1007/s12064-007-0004-x · Cited by 21
Kamble, V. A., & Misra, H. S. (2010) · DNA repair · doi:10.1016/j.dnarep.2010.01.012 · Cited by 21
Kota, S., Kamble, V. A., Rajpurohit, Y. S., & Misra, H. S. (2010) · Biochemistry and Cell Biology · doi:10.1139/o10-075 · Cited by 21
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Ayala-Ortiz, C., Freire-Zapata, V., & Tfaily, M. (2025) · Communications Earth & Environment · doi:10.1038/s43247-025-02637-y · Cited by 20
Bacterial community composition in lakes
Yadav, A. N., Yadav, N., Kour, D., Kumar, A., Yadav, K., Kumar, A., Rastegari, A. A., Sachan, S. G., Singh, B., Chauhan, V. S., et al. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-817495-1.00001-3 · Cited by 23
Radioprotection of nonhuman biota
Delistraty, D. A. (2008) · Journal of Environmental Radioactivity · doi:10.1016/j.jenvrad.2008.09.001 · Cited by 20
Elevated Rate of Genome Rearrangements in Radiation-Resistant Bacteria
Repar, J., Supek, F., Klanjšček, T., Warnecke, T., Zahradka, K., & Zahradka, D. (2017) · Genetics · doi:10.1534/genetics.116.196154 · Cited by 15
Self-citationDouble strand break (DSB) repair in Cyanobacteria: Understanding the process in an ancient organism
Rajaram, H., Kumar, A., Kirti, A., & Pandey, S. (2020) · DNA repair · doi:10.1016/j.dnarep.2020.102942 · Cited by 19
Metadata
- Authors
- Zahradka, K., Slade, D., Bailone, A., Sommer, S., Averbeck, D., Petranovic, M., Lindner, A. B., & Radman, M.
- Affiliations
- Inserm (FR)
- Université Paris-Sud (FR)
- Centre National de la Recherche Scientifique (FR)
- Corresponding author
- Radman, Miroslav
- Venue
- Nature
- Published
- 2006-09-27
- Volume
- 443
- Issue
- 7111
- Pages
- 569-573
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2036099589
- Cited by
- 444
- References
- 30
- Citations by year
- 2026: 13 · 2025: 16 · 2024: 14 · 2023: 27 · 2022: 12 · 2021: 24 · 2020: 24 · 2019: 21 · 2018: 19 · 2017: 13 · 2016: 18 · 2015: 19 · 2014: 26 · 2013: 22 · 2012: 22
- FWCI
- 12.85
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Keywords
- Deinococcus radiodurans, radioresistance (biology), DNA repair, homologous recombination, DNA polymerase I, single-stranded DNA synthesis, genome fragmentation, desiccation tolerance, extremophiles
- MeSH terms
- Bromodeoxyuridine, Chromosomes, Bacterial, Desiccation, DNA Damage, DNA Polymerase I, DNA Repair, DNA Replication, DNA, Bacterial, Models, Genetic, Photolysis, Radiation Tolerance, Genome, Bacterial, Deinococcus
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