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DNA repair in an active gene: Removal of pyrimidine dimers from the DHFR gene of CHO cells is much more efficient than in the genome overall
Abstract
DNA repair was measured in the dihydrofolate reductase gene in Chinese hamster ovary cells, amplified for the gene, by quantitating pyrimidine dimers with a specific UV-endonuclease. More than two thirds of the dimers had been removed from a 14.1 kb restriction fragment of the gene by 26 hr after irradiation (20 J/m2), while little removal was detected in fragments upstream of the gene and only 15% were removed from the genome overall. This suggests that damage processing can vary according to function or activity of affected sequences, which has general implications for correlations of DNA repair with survival and mutagenesis. Perhaps preferential repair of vital sequences facilitates UV-resistance of these cells despite low overall repair levels.
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“XPA is an indispensable factor both for transcription-coupled NER and global genome NER [7], [8].”
From UV-Induced Nuclear Import of XPA Is Mediated by Importin-α4 in An ATR-Dependent Manner (2013) · cites this paper as [7]
In the citing paper
“Two subpathways of NER exist: transcription-blocking lesions in the transcribed strand (TS) of active genes are repaired quickly by transcription-coupled NER (TC-NER), whereas the rest of the genome, including the nontranscribed strand (NTS) of active genes, is repaired more slowly by global genome NER (GG-NER) (8, 33, 34, 44, 54).”
From A Role for Checkpoint Kinase-Dependent Rad26 Phosphorylation in Transcription-Coupled DNA Repair in Saccharomyces cerevisiae (2010) · cites this paper as [8]
Citations
Cites
Detection of specific sequences among DNA fragments separated by gel electrophoresis
Southern, E. M. (1975) · Journal of Molecular Biology · doi:10.1016/s0022-2836(75)80083-0 · Cited by 32,245
A rapid alkaline extraction procedure for screening recombinant plasmid DNA
Birnboim, H. C., & Doly, J. (1979) · Nucleic Acids Research · doi:10.1093/nar/7.6.1513 · Cited by 14,686
Wahl, G. M., Stern, M., & Stark, G. R. (1979) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.76.8.3683 · Cited by 3,159
Calcium-dependent bacteriophage DNA infection
Mandel, M., & Higa, A. (1970) · Journal of Molecular Biology · doi:10.1016/0022-2836(70)90051-3 · Cited by 2,521
[29] Analysis of repeating DNA sequences by reassociation
Britten, R. J., Graham, D. E., & Neufeld, B. R. (1974) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(74)29033-5 · Cited by 1,041
Alt, F. W., Kellems, R. E., Bertino, J. R., & SCHIMKE, R. T. (1978) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)34875-5 · Cited by 934
DNA Repair in Bacteria and Mammalian Cells
Hanawalt, P. C., Cooper, P. K., Ganesan, A. K., & Smith, C. A. (1979) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.48.070179.004031 · Cited by 837
Gene amplification in cultured animal cells
SCHIMKE, R. T. (1984) · Cell · doi:10.1016/0092-8674(84)90406-9 · Cited by 635
Practical Methods in Molecular Biology
Schleif, R., & Wensink, P. C. (1981) · Springer eBooks · doi:10.1007/978-1-4612-5956-5 · Cited by 473
Sequence organization of the human genome
Schmid, C. W., & Deininger, P. L. (1975) · Cell · doi:10.1016/0092-8674(75)90184-1 · Cited by 301
Cited by
Sorted by citations
Items 601–700 of 1,001
Gospodinov, A. G., & Herceg, Z. (2012) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2012.10.001 · Cited by 28
“Based on differences in lesion recognition, NER is divided into two subpathways–the more efficient transcription coupled repair (TC-NER), which is involved in the repair of the transcribed strand of active genes [32,33] and global genome repair (GG-NER), responsible for repair of all other parts of the genome.”
BackgroundAguilar‐Fuentes, J., Fregoso, M., Herrera‐Cruz, M., Reynaud, E., Braun, C., Egly, J., & Zurita, M. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.1000253 · Cited by 28
Differential mutation of transgenic and endogenous loci in vivo
Cosentino, L., & Heddle, J. A. (2000) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(00)00125-1 · Cited by 28
Reynaud, E., Lomelı́, H., Vâzquez, M., & Zurita, M. (1999) · Molecular Biology of the Cell · doi:10.1091/mbc.10.4.1191 · Cited by 28
“However, it is possible that regions that are highly transcribed are more sensitive to suffering damage from different physical and chemical agents (Bohr et al., 1985); therefore, the NER complex should be recruited to repair the puffs as well.”
Deng, W., & Nickoloff, J. A. (1994) · Molecular and Cellular Biology · doi:10.1128/mcb.14.1.391 · Cited by 28
Role of transcription-coupled DNA repair in susceptibility to environmental carcinogenesis.
Hanawalt, P. C. (1996) · Environmental Health Perspectives · doi:10.1289/ehp.96104s3547 · Cited by 28
Genomic Stability and Instability: A Working Paradigm
Cheng, K. C., & Loeb, L. A. (1997) · Current topics in microbiology and immunology · doi:10.1007/978-3-642-60505-5_2 · Cited by 28
Yasuhira, S., Mitani, H., & Shima, A. (1992) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1992.tb04214.x · Cited by 28
Repair of transcriptionally active and inactive genes during S and G2 phases of the cell cycle
Russev, G. C., & Boulikas, T. (1992) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1992.tb16633.x · Cited by 28
Shaposhnikov, S. A., Thomsen, P. D., & Collins, A. R. (2010) · Methods in molecular biology · doi:10.1007/978-1-60327-409-8_10 · Cited by 27
Mitotic viability and metabolic competence in UV-irradiated yeast cells
Conconi, A., Jäger-Vottero, P., Zhang, X., Beard, B. C., & Smerdon, M. J. (2000) · Mutation Research/DNA Repair · doi:10.1016/s0921-8777(99)00057-9 · Cited by 27
Preferential Repair of DNA Double-strand Break at the Active Gene in Vivo
Chaurasia, P., Sen, R., Pandita, T. K., & Bhaumik, S. R. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.364661 · Cited by 27
Transcription response and nucleotide excision repair
Mullenders, L. H. F. (1998) · Mutation Research/DNA Repair · doi:10.1016/s0921-8777(98)00048-2 · Cited by 27
Drobetsky, E. A., Grosovsky, A. J., Skandalis, A., & Glickman, B. W. (1989) · Somatic Cell and Molecular Genetics · doi:10.1007/bf01534891 · Cited by 27
Seroz, T. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.22.4506 · Cited by 27
Molecular analysis of Saccharomyces cerevisiae chromosome I
Harris, S. D., Cheng, J. M., Pugh, T. A., & Pringle, J. R. (1992) · Journal of Molecular Biology · doi:10.1016/0022-2836(92)91025-k · Cited by 27
“…for differential repair in the genomes of yeast, humans, and Chinese hamster ovary cells; in particular, DNA sequences t’hat are transcriptionally active appear to be more efficiently repaired in these organisms (Bohr et al., 1985; Mellon et aZ., 1987; Leadon $ Snowden, 1988; Terleth et al., 1990).”
BackgroundIntranuclear localization of UV-induced DNA repair in human VA13 cells
Harless, J., & Hewitt, R. R. (1987) · Mutation Research/DNA Repair Reports · doi:10.1016/0167-8817(87)90060-5 · Cited by 27
Distribution of initial and persistent 2-acetylaminofluorene-induced DNA adducts within DNA loops.
Gupta, R. C., Dighe, N. R., Randerath, K., & Smith, H. C. (1985) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.82.19.6605 · Cited by 27
UV-Induced Nuclear Import of XPA Is Mediated by Importin-α4 in An ATR-Dependent Manner
Li, Z., Musich, P. R., Cartwright, B. M., Wang, H., & Zou, Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0068297 · Cited by 26
Nucleotide excision repair of aflatoxin-induced DNA damage within the 3D human genome organization
Wu, Y., Adeel, M. M., Xia, D., Sancar, A., & Li, W. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae755 · Cited by 28
“The effect of transcription on nucleotide excision repair has been extensively studied since the discovery of TCR in human cells ( 59 ).”
BackgroundLin, P. S., McPherson, L. A., Chen, A. Y., Sage, J., & Ford, J. M. (2009) · DNA repair · doi:10.1016/j.dnarep.2009.03.003 · Cited by 27
Tu, Y., Bates, S., & Pfeifer, G. P. (1998) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(98)00038-4 · Cited by 26
Tremblay, M., Charton, R., Wittner, M., Levasseur, G., Griesenbeck, J., & Conconi, A. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt871 · Cited by 25
Conceptual developments in the causes of Cockayne syndrome
Cleaver, J. E., Bezrookove, V., Revet, I. M., & Huang, E. J. (2013) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2013.02.005 · Cited by 29
“strand than in the nontranscribed strand (Bohr et al., 1985; Mellon et al., 1987).”
Rangaswamy, S., Pandey, A., MITRA, S. P., & Hegde, M. L. (2017) · Genes · doi:10.3390/genes8070175 · Cited by 26
Transcription-Coupled Repair: From Cells to Single Molecules and Back Again
Strick, T. R., & Portman, J. R. (2019) · Journal of Molecular Biology · doi:10.1016/j.jmb.2019.05.040 · Cited by 26
Tommasi, S. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.20.3991 · Cited by 26
Nairn, R. S., Mitchell, D. L., Adair, G. M., Thompson, L. H., Siciliano, M. J., & Humphrey, R. M. (1989) · Mutation Research/DNA Repair · doi:10.1016/0921-8777(89)90071-2 · Cited by 26
Decreased DNA repair in familial Alzheimer's disease
Jones, S. K., Nee, L. E., Sweet, L. M., Polinsky, R. J., Bartlett, J. D., Bradley, W. G., & Robison, S. H. (1989) · Mutation Research/DNAging · doi:10.1016/0921-8734(89)90007-6 · Cited by 26
Hoogervorst, E. M., van Oostrom, C. T. M., Beems, R. B., van Benthem, J., van den Berg, J., van Kreijl, C. F., Vos, J. G., de Vries, A., & STEEG, H. V. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.08.009 · Cited by 27
Dresler, S. L. (1985) · Biochemistry · doi:10.1021/bi00345a019 · Cited by 26
UV-induced photolesions, their repair and mutations
Mullenders, L. H. F., Dokkum, A. M. H.-V., Kalle, W. H. J., Vrieling, H., Zdzienicka, M. Z., & van Zeeland, A. A. (1993) · Mutation Research/Genetic Toxicology · doi:10.1016/0165-1218(93)90103-k · Cited by 26
Down modulation of topoisomerase I affects DNA repair efficiency
Mao, Y. (2003) · DNA repair · doi:10.1016/s1568-7864(03)00122-8 · Cited by 28
Human repair gene restores normal pattern of preferential DNA repair in repair defective CHO cells
Bohr, V. A., Chu, E. H. Y., van Duin, M., Hanawalt, P. C., & Okumoto, D. S. (1988) · Nucleic Acids Research · doi:10.1093/nar/16.15.7397 · Cited by 26
Self-citationde Cock, J. G. R., Klink, E. C., Ferro, W., Lohman, P. H. M., & Eeken, J. C. J. (1992) · Mutation Research/DNA Repair · doi:10.1016/0921-8777(92)90003-l · Cited by 26
Niggli, H. J., Bayreuther, K., Rodemann, H. P., Röthlisberger, R., & Francz, P. I. (1989) · Mutation Research/DNAging · doi:10.1016/0921-8734(89)90005-2 · Cited by 26
Carothers, A. M., Zhen, W. K., Mucha, J., Zhang, Y. J., Santella, R. M., Grünberger, D., & Bohr, V. A. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.24.11925 · Cited by 26
Self-citationFutscher, B. W., Pieper, R., Dalton, W., & Erickson, L. C. (1992) · PubMed · Cited by 26
Pines, A., Backendorf, C., Alekseev, S., Jansen, J. G., de Gruijl, F. R., Vrieling, H., & Mullenders, L. H. F. (2008) · DNA repair · doi:10.1016/j.dnarep.2008.09.011 · Cited by 25
Unscheduled DNA Synthesis: A Functional Assay for Global Genomic Nucleotide Excision Repair
Kelly, C. M., & Latimer, J. J. (2004) · Humana Press eBooks · doi:10.1385/1-59259-840-4:303 · Cited by 25
Strand Breaks Are Repaired Efficiently in Human Ribosomal Genes
Fritz, L. K., Suquet, C., & Smerdon, M. J. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.22.12972 · Cited by 25
“The yield of CPDs in each strand of the 7.2-kb rDNA fragment was measured using the method of Bohr et al. (1985).”
MethodInfluentialXeroderma pigmentosum complementation group F in a non-Japanese patient
Norris, P. G., Hawk, J. L. M., Avery, J., & Giannelli, F. (1988) · Journal of the American Academy of Dermatology · doi:10.1016/s0190-9622(88)70121-8 · Cited by 25
Bunch, R. T., Gewirtz, D. A., & Povirk, L. F. (1995) · International Journal of Radiation Biology · doi:10.1080/09553009514551541 · Cited by 25
Assessment of DNA damage and repair in specific genomic regions by quantitative immuno-coupled PCR
Denissenko, M. F., Venkatachalam, S., Yamasaki, E. F., & Wani, A. A. (1994) · Nucleic Acids Research · doi:10.1093/nar/22.12.2351 · Cited by 25
Differential role of RB in response to UV and IR damage
Bosco, E. E. (2005) · Nucleic Acids Research · doi:10.1093/nar/gki283 · Cited by 24
Post-Transcriptional Regulation of DNA Damage-Responsive Gene Expression
McKay, B. C. (2013) · Antioxidants and Redox Signaling · doi:10.1089/ars.2013.5523 · Cited by 25
Transcription-coupled repair and the transcriptional response to UV-Irradiation
Gaul, L., & Svejstrup, J. Q. (2021) · DNA repair · doi:10.1016/j.dnarep.2021.103208 · Cited by 22
XPF activates break-induced telomere synthesis
Guh, C.-Y., Shen, H.-J., Chen, L. W., Chiu, P.-C., Liao, I.-H., Lo, C.-C., Chen, Y., Hsieh, Y.-H., Chang, T.-C., Yen, C.-P., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-33428-0 · Cited by 25
Role of DNA repair in the protection against genotoxic stress
Camenisch, U., & Naegeli, H. (2009) · Proceedings of the Fourth International Symposium on Polarization Phenomena in Nuclear Reactions · doi:10.1007/978-3-7643-8336-7_5 · Cited by 24
Tremblay, M., Teng, Y., Paquette, M., Waters, R., & Conconi, A. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.00137-08 · Cited by 24
Global-genome Nucleotide Excision Repair Controlled by Ubiquitin/Sumo Modifiers
Rüthemann, P., Pogliano, C. B., & Naegeli, H. (2016) · Frontiers in Genetics · doi:10.3389/fgene.2016.00068 · Cited by 28
“The TC-NER pathway is initiated when an RNA polymerase II complex encounters obstructing base lesions (Bohr et al., 1985).”
BackgroundNucleotide Excision Repair and its Connection with Cancer and Ageing
Andressoo, J., Hoeijmakers, J. H. J., & de Waard, H. (2006) · Springer eBooks · doi:10.1007/1-4020-3764-3_3 · Cited by 26
In vitro eukaryotic DNA excision repair assays: An overview
Salles, B. (1995) · Biochimie · doi:10.1016/0300-9084(96)88198-3 · Cited by 24
STUSCHKE, A. S. M. (1998) · International Journal of Radiation Biology · doi:10.1080/095530098142680 · Cited by 24
Maddukuri, L., Dudzińska, D., & Tudek, B. (2007) · Acta Biochimica Polonica · doi:10.18388/abp.2007_3222 · Cited by 24
“For the first time, TCR was described in mammalian cells by Bohr and co-workers and by Mellon and Hanawalt who observed that the removal of DNA lesions from the transcribed strands of active genes is much more efficient than from the whole genome (Bohr et al., 1985; Mellon & Hanawalt, 1989).”
BackgroundMacLeod, M. C., Daylong, A., Adair, G. M., & Humphrey, R. M. (1991) · Mutation Research/Genetic Toxicology · doi:10.1016/0165-1218(91)90042-k · Cited by 24
Conconi, A., Liu, X., Koriazova, L., Ackerman, E. J., & Smerdon, M. J. (1999) · The EMBO Journal · doi:10.1093/emboj/18.5.1387 · Cited by 24
“As first discovered in Chinese hamster ovary cells (Bohr et al., 1985), and subsequently in several other organisms (Mellon and Hanawalt, 1989; Smerdon and Thoma, 1990), NER occurs preferentially in many transcriptionally active genes (reviewed in Friedberg, 1996).”
BackgroundBhattacharyya, N. P., Maher, V. M., & McCormick, J. J. (1989) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/0027-5107(89)90003-1 · Cited by 24
The biology of radioresistance: similarities, differences and interactions with drug resistance
Powell, S. N., & Abraham, E. H. (1993) · Cytotechnology · doi:10.1007/bf00744671 · Cited by 24
Zheng, Y., Pao, A., Adair, G. M., & Tang, M. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m010973200 · Cited by 24
Regan, J. D., Thompson, L. H., Carrier, W. L., Weber, C. A., Francis, A. A., & Zdzienicka, M. Z. (1990) · Mutation Research/DNA Repair · doi:10.1016/0921-8777(90)90069-h · Cited by 24
Transcription-Coupled DNA Repair
Hanawalt, P. C., & Spivak, G. (1999) · Springer eBooks · doi:10.1007/978-1-4615-4865-2_14 · Cited by 24
Leadon, S. A. (1987) · Europe PMC (PubMed Central) · Cited by 24
Intragenomic Heterogeneity in DNA Damage Processing: Potential Implications for Risk Assessment
Hanawalt, P. C. (1986) · Springer eBooks · doi:10.1007/978-1-4615-9462-8_51 · Cited by 24
Brugger, C., Zhang, C., Suhanovsky, M. M., Kim, D. D., Sinclair, A. N., Lyumkis, D., & Deaconescu, A. M. (2020) · Nature Communications · doi:10.1038/s41467-020-17457-1 · Cited by 23
Analysis of DNA Repair Using Transfection-Based Host Cell Reactivation
Johnson, J. M., & Latimer, J. J. (2004) · Humana Press eBooks · doi:10.1385/1-59259-840-4:321 · Cited by 23
van Zeeland, A. A., Vreeswijk, M. P. G., de Gruijl, F. R., van Kranen, H. J., Vrieling, H., & Mullenders, L. H. F. (2005) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2005.03.018 · Cited by 23
Pitfalls of the most commonly used models of context dependent substitution
Lindsay, H. A., Yap, V. B., Ying, H., & Huttley, G. A. (2008) · Biology Direct · doi:10.1186/1745-6150-3-52 · Cited by 23
“The strand asymmetry in support and MLEs of context effects is consistent with previous reports [31] and likely reflects the influence of transcription coupled DNA repair (TCR) processes, which selectively repair the transcribed strand [32].”
ResultMeasuring the Formation and Repair of UV Damage at the DNA Sequence Level by Ligation-Mediated PCR
Nia, A. B., & Pfeifer, G. P. (2012) · Methods in molecular biology · doi:10.1007/978-1-61779-998-3_14 · Cited by 23
Proietti‐De‐Santis, L., Garcia, C. L., Balajee, A. S., Brea‐Calvo, G., Bassi, L., & Palitti, F. (2001) · Mutation Research/DNA Repair · doi:10.1016/s0921-8777(00)00065-3 · Cited by 23
The Molecular Genetics of the Incision Step in the DNA Excision Repair Process
Rubin, J. S. (1988) · International Journal of Radiation Biology · doi:10.1080/09553008814551751 · Cited by 23
Repair of Oxidative DNA Damage In Vitro: A Tool for Screening Antioxidative Compounds
Salles, B., Sattler, U., Bozzato, C., & Calsou, P. (1999) · Food and Chemical Toxicology · doi:10.1016/s0278-6915(99)00094-0 · Cited by 23
Can DNA repair cause enhanced cell killing following treatment with ionizing radiation?
Harrison, L., & Malyarchuk, S. (2002) · Pathophysiology · doi:10.1016/s0928-4680(01)00079-7 · Cited by 23
“[65] V.”
BackgroundChen, Y. H., Matsumoto, Y., Shibutani, S., & Bogenhagen, D. F. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.21.9583 · Cited by 23
Molecular characterization of an acidic region deletion mutant of Cockayne syndrome group B protein
Sunesen, M. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.16.3151 · Cited by 23
Mullenders, L. H. F., van Zeeland, A. A., & Natarajan, A. T. (1987) · Journal of Cell Science · doi:10.1242/jcs.1984.supplement_6.17 · Cited by 23
Karentz, D., & Cleaver, J. E. (1986) · Mutation Research/DNA Repair Reports · doi:10.1016/0167-8817(86)90051-9 · Cited by 23
Habraken, Y., & Laval, F. (1993) · Mutation Research/DNA Repair · doi:10.1016/0921-8777(93)90069-s · Cited by 23
Komura, J., Mitani, H., Nemoto, N., Ishikawa, T., & Shima, A. (1991) · Mutation Research/DNA Repair · doi:10.1016/0921-8777(91)90056-u · Cited by 23
DNA‐Directed Mutations: Leading and Lagging Strand Specificity
Sinden, R. R., Hashem, V. I., & Rosche, W. A. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb08878.x · Cited by 23
Martomo, S. A., Fu, D., Yang, W. W., Joshi, N. S., & Gearhart, P. J. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.12.7787 · Cited by 23
“To detect dU in a specific gene, we modified an established Southern blot technique, which has been used previously to study genespecific DNA repair in mammalian cells (26, 27).”
MethodTemperature dependence of adriamycin-induced DNA damage in L1210 cells.
Vichi, P., Robison, S., & Tritton, T. R. (1989) · PubMed · Cited by 23
Hochleitner, K., Thomale, J., Nikitin, A. Y., & Rajewsky, M. F. (1991) · Nucleic Acids Research · doi:10.1093/nar/19.16.4467 · Cited by 23
Perozzi, G., & Prakash, S. (1986) · Molecular and Cellular Biology · doi:10.1128/mcb.6.5.1497-1507.1986 · Cited by 23
McKay, B. C., & Rainbow, A. J. (1996) · Mutation Research/DNA Repair · doi:10.1016/0921-8777(96)00013-4 · Cited by 23
Filipski, J., Salinas, J., & RODIER, F. (1987) · DNA · doi:10.1089/dna.1987.6.109 · Cited by 23
“Part of the regional differences in composition may be explained by different rates of repair in active genes versus the overall genome (Bohr et al., 1985).”
Saxena, J. K., Hays, J. B., & Ackerman, E. J. (1990) · Nucleic Acids Research · doi:10.1093/nar/18.24.7425 · Cited by 23
Transcription Blockage by DNA Damage in Nucleotide Excision Repair-Related Neurological Dysfunctions
Kajitani, G. S., Nascimento, L. L. D. S., Neves, M. R. D. C., Leandro, G. D. S., Garcia, C. C. M., & Menck, C. F. M. (2021) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2020.10.009 · Cited by 22
Photobiological Origins of the Field of Genomic Maintenance
Ganesan, A., & Hanawalt, P. (2016) · Photochemistry and Photobiology · doi:10.1111/php.12542 · Cited by 22
A half century of exploring DNA excision repair in chromatin
Smerdon, M. J., Wyrick, J. J., & Delaney, S. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.105118 · Cited by 25
Mosesso, P., Palitti, F., Pepe, G., Piñero, J., Bellacima, R., Ahnström, G., & Natarajan, A. T. (2010) · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · doi:10.1016/j.mrgentox.2010.03.005 · Cited by 22
New discoveries linking transcription to DNA repair and damage tolerance pathways
Cohen, S., & Walker, G. C. (2011) · Transcription · doi:10.4161/trns.2.1.14228 · Cited by 22
Base Excision Repair and Nucleotide Excision Repair
Izumi, T., & Mellon, I. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803309-8.00017-3 · Cited by 22
Damage removal and gap filling in nucleotide excision repair
Kemp, M. G. (2019) · The Enzymes · doi:10.1016/bs.enz.2019.06.001 · Cited by 27
Rey, J.-P., Scott, R. J., & Müller, H. (1993) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/0027-5107(93)90067-p · Cited by 22
Defective nucleotide excision repair in yeast hpr1 and tho2 mutants
González‐Barrera, S. (2002) · Nucleic Acids Research · doi:10.1093/nar/30.10.2193 · Cited by 22
Deletion of the CSB homolog, RAD26, yields Spt- strains with proficient transcription-coupled repair
Gregory, S. M. (2001) · Nucleic Acids Research · doi:10.1093/nar/29.14.3080 · Cited by 22
“(6,19, 22 ). Equal amounts of purified, restricted DNA were either mock treated (10 mM Tris–HCl, pH 7.5, 0.1 M NaCl, 10 mM EDTA, 1 mg/ml BSA) or treated with the enzyme T4 endonuclease V in mock buffer for 30 min at 37°C.”
MethodInfluentialTwo-Wavelength Fluorescence Assay for DNA Repair
Roguev, A., & Russev, G. C. (2000) · Analytical Biochemistry · doi:10.1006/abio.2000.4865 · Cited by 22
Hu, W., Feng, Z., Chasin, L. A., & Tang, M. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m206375200 · Cited by 22
Rehman, I., Lowry, D. T., Adams, C., Abdel‐Fattah, R., Holly, A. J., Yuspa, S. H., & Hennings, H. (2000) · Molecular Carcinogenesis · doi:10.1002/(sici)1098-2744(200004)27:4 · Cited by 29
Metadata
- Authors
- Bohr, V
- Affiliations
- Stanford University (US)
- Corresponding author
- Bohr, V
- ORCID
- Bohr, V
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 1985-02
- Volume
- 40
- Issue
- 2
- Pages
- 359-369
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W1984353960
- Cited by
- 1,237
- References
- 34
- Citations by year
- 2026: 11 · 2025: 17 · 2024: 15 · 2023: 14 · 2022: 12 · 2021: 17 · 2020: 18 · 2019: 11 · 2018: 18 · 2017: 13 · 2016: 23 · 2015: 9 · 2014: 24 · 2013: 24 · 2012: 22
- FWCI
- 15.13
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of General Medical Sciences (GM 09901)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Carcinogens and Genotoxicity Assessment
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Effects of Radiation Exposure
- Keywords
- DNA repair, pyrimidine dimers, dihydrofolate reductase gene, UV-induced DNA damage, UV endonuclease, UV resistance, CHO cells, mutagenesis, cell survival
- MeSH terms
- Animals, Base Sequence, Cell Line, Cell Survival, Cricetulus, DNA Repair, Endodeoxyribonucleases, Female, Cricetinae, Multienzyme Complexes, N-Glycosyl Hydrolases, Pyrimidine Dimers, Tetrahydrofolate Dehydrogenase
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