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A multistep damage recognition mechanism for global genomic nucleotide excision repair
Open accessAbstract
A mammalian nucleotide excision repair (NER) factor, the XPC–HR23B complex, can specifically bind to certain DNA lesions and initiate the cell-free repair reaction. Here we describe a detailed analysis of its binding specificity using various DNA substrates, each containing a single defined lesion. A highly sensitive gel mobility shift assay revealed that XPC–HR23B specifically binds a small bubble structure with or without damaged bases, whereas dual incision takes place only when damage is present in the bubble. This is evidence that damage recognition for NER is accomplished through at least two steps; XPC–HR23B first binds to a site that has a DNA helix distortion, and then the presence of injured bases is verified prior to dual incision. Cyclobutane pyrimidine dimers (CPDs) were hardly recognized by XPC–HR23B, suggesting that additional factors may be required for CPD recognition. Although the presence of mismatched bases opposite a CPD potentiated XPC–HR23B binding, probably due to enhancement of the helix distortion, cell-free excision of such compound lesions was much more efficient than expected from the observed affinity for XPC–HR23B. This also suggests that additional factors and steps are required for the recognition of some types of lesions. A multistep mechanism of this sort may provide a molecular basis for ensuring the high level of damage discrimination that is required for global genomic NER.
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“hHR23B-XPC complex or only XPC exhibits a similar high affinity for both UV-induced single-stranded DNA (ssDNA) and double-stranded DNA (dsDNA) [230, 259], preferentially binds to DNA with various lesions [259] and even to small bubble structures with or without a lesion [260].”
From Molecular Mechanisms of Ultraviolet Radiation‐Induced DNA Damage and Repair (2010) · cites this paper as [260]
In the citing paper
“whereas 6-4PP lesions are directly recognized by XPC independent of DDB [5–8].”
From ATR- and ATM-Mediated DNA Damage Response Is Dependent on Excision Repair Assembly during G1 but Not in S Phase of Cell Cycle (2016) · cites this paper as [7]
In the citing paper
“The DDB complex initially recognizes the CPD lesions and helps in recruiting XPC”
From ATR- and ATM-Mediated DNA Damage Response Is Dependent on Excision Repair Assembly during G1 but Not in S Phase of Cell Cycle (2016) · cites this paper as [7]
In the citing paper
“In turn, XPC helps in recruiting XPA, XPG, and TFIIH components that enable opening of the DNA helix around the damage site to form a bubble [8].”
From NER initiation factors, DDB2 and XPC, regulate UV radiation response by recruiting ATR and ATM kinases to DNA damage sites (2013) · cites this paper as [8]
In the citing paper
“The DDB complex initially recognizes the CPD lesions and recruits XPC [4, 5, 8, 9], whereas XPC can independently recognize 6-4PP lesions [5].”
From NER initiation factors, DDB2 and XPC, regulate UV radiation response by recruiting ATR and ATM kinases to DNA damage sites (2013) · cites this paper as [8]
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Cites
3 retracted
Cooper, P. K., Nouspikel, T. P., Clarkson, S. G., & Leadon, S. A. (1997) · Science · doi:10.1126/science.275.5302.990 · Cited by 306
RetractedRETRACTED: Transcription-Coupled Repair of 8-oxoGuanine
Page, F. L., Kwoh, E. E., Avrutskaya, A. V., Gentil, A., Leadon, S. A., Sarasin, A. R., & Cooper, P. K. (2000) · Cell · doi:10.1016/s0092-8674(00)80827-2 · Cited by 280
RetractedPage, F. L., Kwoh, E. E., Avrutskaya, A. V., Gentil, A., Leadon, S. A., Sarasin, A. R., & Cooper, P. K. (2005) · Cell · doi:10.1016/j.cell.2005.11.005 · Cited by 271
RetractedThe Metabolic Basis of Inherited Disease.
(1988) · Annals of Internal Medicine · doi:10.7326/0003-4819-108-3-503_7 · Cited by 7,807
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
Bohr, V (1985) · Cell · doi:10.1016/0092-8674(85)90150-3 · Cited by 1,237 · cited 1×
“In contrast, TCR specifically removes lesions that block RNA polymerases on the transcribed strands of active genes (Bohr et al. 1985; Mellon et al. 1987).”
BackgroundMELLON, I. (1987) · Cell · doi:10.1016/0092-8674(87)90151-6 · Cited by 1,228
Sugasawa, K., Ng, J. M. Y., Masutani, C., Iwai, S., van der Spek, P. J., Eker, A. P. M., Hanaoka, F., Bootsma, D., & Hoeijmakers, J. H. J. (1998) · Molecular Cell · doi:10.1016/s1097-2765(00)80132-x · Cited by 899
Self-citationDNA Repair Helicase: a Component of BTF2 (TFIIH) Basic Transcription Factor
Schaeffer, L., Roy, R., Humbert, S., Moncollin, V., Vermeulen, W., Hoeijmakers, J. H. J., Chambon, P., & Egly, J. (1993) · Science · doi:10.1126/science.8465201 · Cited by 794
THE BIOLOGY OF THE (6–4) PHOTOPRODUCT
MITCHELL, D. L., & NAIRN, R. S. (1989) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1989.tb05578.x · Cited by 592
Flagged first, then by citations
Research works printed but not linked: 1
- Naegeli H. (1999) Enzymology of human nucleotide excision repair. in DNA recombination and repair, eds Smith P. Jones C. (Oxford University Press, Oxford, UK), pp 99–137.
Cited by
Sorted by citations
Genome maintenance mechanisms for preventing cancer
Hoeijmakers, J. H. J. (2001) · Nature · doi:10.1038/35077232 · Cited by 3,939
Molecular Mechanisms of Mammalian DNA Repair and the DNA Damage Checkpoints
Sancar, A., Lindsey-Boltz, L. A., Ünsal-Kaçmaz, K., & Linn, S. (2004) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.73.011303.073723 · Cited by 3,317
DNA repair pathways as targets for cancer therapy
Helleday, T., Petermann, E., Lundin, C., Hodgson, B., & Sharma, R. A. (2008) · Nature Reviews Cancer · doi:10.1038/nrc2342 · Cited by 1,666
Molecular Mechanisms of Ultraviolet Radiation‐Induced DNA Damage and Repair
Rastogi, R. P., Richa, Kumar, A., Tyagi, M. B., & Sinha, R. P. (2010) · Journal of Nucleic Acids · doi:10.4061/2010/592980 · Cited by 1,329
“hHR23B-XPC complex or only XPC exhibits a similar high affinity for both UV-induced single-stranded DNA (ssDNA) and double-stranded DNA (dsDNA) [230, 259], preferentially binds to DNA with various lesions [259] and even to small bubble structures with or without a lesion [260].”
BackgroundUnderstanding nucleotide excision repair and its roles in cancer and ageing
Marteijn, J. A., Lans, H., Vermeulen, W., & Hoeijmakers, J. H. J. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3822 · Cited by 1,192
Nucleotide Excision Repair in EukaryotesPreprint
Schärer, O. D. (2013) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a012609 · Cited by 863
Sequential Assembly of the Nucleotide Excision Repair Factors In Vivo
Volker, M., Moné, M. J., Karmakar, P., van Hoffen, A., Schul, W., Vermeulen, W., Hoeijmakers, J. H. J., DRIEL, R. V., van Zeeland, A. A., & Mullenders, L. H. F. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00281-7 · Cited by 782
How nucleotide excision repair protects against cancer
Friedberg, E. C. (2001) · Nature Reviews Cancer · doi:10.1038/35094000 · Cited by 730
Molecular Mechanisms of Mammalian Global Genome Nucleotide Excision Repair
Gillet, L. C. J., & Schärer, O. D. (2006) · Chemical Reviews · doi:10.1021/cr040483f · Cited by 642
UV-Induced Ubiquitylation of XPC Protein Mediated by UV-DDB-Ubiquitin Ligase Complex
Sugasawa, K., Okuda, Y., Saijo, M., Nishi, R., Matsuda, N., Chu, G., Mori, T., Iwai, S., Tanaka, K., Tanaka, K., et al. (2005) · Cell · doi:10.1016/j.cell.2005.02.035 · Cited by 576
Self-citationMechanisms of human DNA repair: an update
Christmann, M., Tomicic, M. T., Roos, W. P., & Kaina, B. (2003) · Toxicology · doi:10.1016/s0300-483x(03)00287-7 · Cited by 599
Fousteri, M., & Mullenders, L. H. (2008) · Cell Research · doi:10.1038/cr.2008.6 · Cited by 487
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Fischer, E. S., Scrima, A., Böhm, K., Matsumoto, S., Lingaraju, G. M., Faty, M., Yasuda, T., Cavadini, S., Wakasugi, M., Hanaoka, F., et al. (2011) · Cell · doi:10.1016/j.cell.2011.10.035 · Cited by 460
Self-citationRecognition of DNA damage by the Rad4 nucleotide excision repair protein
Min, J., & Pavletich, N. P. (2007) · Nature · doi:10.1038/nature06155 · Cited by 431
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Costa, R. (2003) · Biochimie · doi:10.1016/j.biochi.2003.10.017 · Cited by 373
Reardon, J. T., & Sancar, A. (2005) · Progress in Nucleic Acid Research and Molecular Biology · doi:10.1016/s0079-6603(04)79004-2 · Cited by 350
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Compe, E., & Egly, J. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3350 · Cited by 357
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McKinnon, P. J. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2559 · Cited by 323
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Giglia‐Mari, G., & Sarasin, A. R. (2003) · Human Mutation · doi:10.1002/humu.10179 · Cited by 298
Coordination of dual incision and repair synthesis in human nucleotide excision repair
Staresincic, L., Fagbemi, A. F., Enzlin, J. H., Gourdin, A. M., Wijgers, N., Dunand‐Sauthier, I., Giglia‐Mari, G., Clarkson, S. G., Vermeulen, W., & Schärer, O. D. (2009) · The EMBO Journal · doi:10.1038/emboj.2009.49 · Cited by 287
Eukaryotic nucleotide excision repair: from understanding mechanisms to influencing biology
Shuck, S. C., Short, E. A., & Turchi, J. J. (2008) · Cell Research · doi:10.1038/cr.2008.2 · Cited by 289
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D'Errico, M., Parlanti, E., Teson, M., de Jesus, B. M. B., Degan, P., Calcagnile, A., Jaruga, P., Bjørås, M., Crescenzi, M., Pedrini, A. M., et al. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601277 · Cited by 271
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Horrell, E. M. W., Boulanger, M. C., & D'Orazio, J. A. (2016) · Frontiers in Genetics · doi:10.3389/fgene.2016.00095 · Cited by 285
Ng, J. M. Y., Vermeulen, W., van der Horst, G. T. J., Bergink, S., Sugasawa, K., Vrieling, H., & Hoeijmakers, J. H. J. (2003) · Genes & Development · doi:10.1101/gad.260003 · Cited by 259
Self-citationDNA Damage and Associated DNA Repair Defects in Disease and Premature Aging
Tiwari, V., & Wilson, D. M. (2019) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2019.06.005 · Cited by 244
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Pines, A., Vrouwe, M. G., Marteijn, J. A. F., Typas, D., Luijsterburg, M. S., Cansoy, M., Hensbergen, P. J., Deelder, A. M., de Groot, A., Matsumoto, S., et al. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201112132 · Cited by 280
Self-citationNishi, R., Okuda, Y., Watanabe, E., Mori, T., Iwai, S., Masutani, C., Sugasawa, K., & Hanaoka, F. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.13.5664-5674.2005 · Cited by 249
Self-citationOxidative DNA damage and nucleotide excision repair
Melis, J. P. M., van Steeg, H., & Luijten, M. (2013) · Antioxidants & Redox Signaling · doi:10.1089/ars.2012.5036 · Cited by 234
Le May, N., Mota-Fernandes, D., Vélez-Cruz, R., Iltis, I., Biard, D., & Egly, J. M. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.03.004 · Cited by 228
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Boiteux, S., & Jinks-Robertson, S. (2013) · Genetics · doi:10.1534/genetics.112.145219 · Cited by 250
Wakasugi, M., Kawashima, A., Morioka, H., Linn, S., Sancar, A., Mori, T., Nikaido, O., & Matsunaga, T. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.c100610200 · Cited by 227
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Wolski, S. C., Kuper, J., Hänzelmann, P., Truglio, J. J., Croteau, D. L., Houten, B. V., & Kisker, C. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060149 · Cited by 224
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Lahtz, C., & Pfeifer, G. P. (2011) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjq053 · Cited by 227
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Lans, H., Marteijn, J. A. F., & Vermeulen, W. (2012) · Epigenetics & Chromatin · doi:10.1186/1756-8935-5-4 · Cited by 230
Sugasawa, K., Akagi, J.-I., Nishi, R., Iwai, S., & Hanaoka, F. (2009) · Molecular Cell · doi:10.1016/j.molcel.2009.09.035 · Cited by 205
Self-citationDubaele, S., Proietti‐De‐Santis, L., Bienstock, R. J., Keriel, A., Stefanini, M., Houten, B. V., & Egly, J. (2003) · Molecular Cell · doi:10.1016/s1097-2765(03)00182-5 · Cited by 204
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Tang, J. Y., & Chu, G. (2002) · DNA repair · doi:10.1016/s1568-7864(02)00052-6 · Cited by 208
Sugasawa, K., Shimizu, Y., Iwai, S., & Hanaoka, F. (2002) · DNA repair · doi:10.1016/s1568-7864(01)00008-8 · Cited by 186
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Adimoolam, S., & Ford, J. M. (2003) · DNA Repair · doi:10.1016/s1568-7864(03)00087-9 · Cited by 181
Reardon, J. T., & Sancar, A. (2003) · Genes & Development · doi:10.1101/gad.1131003 · Cited by 179
Saxowsky, T. T., & Doetsch, P. W. (2006) · Chemical Reviews · doi:10.1021/cr040466q · Cited by 179
Wu, X. (2003) · Carcinogenesis · doi:10.1093/carcin/24.3.505 · Cited by 175
Rapić-Otrin, V. (2002) · Nucleic Acids Research · doi:10.1093/nar/30.11.2588 · Cited by 175
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Dinant, C., de Jager, M., Essers, J., van Cappellen, W. A., Kanaar, R., Houtsmuller, A. B., & Vermeulen, W. (2007) · Journal of Cell Science · doi:10.1242/jcs.004523 · Cited by 172
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Wang, Q.-E. (2005) · Nucleic Acids Research · doi:10.1093/nar/gki684 · Cited by 160
Li, C., Gołębiowski, F., Onishi, Y., Samara, N. L., Sugasawa, K., & Yang, W. (2015) · Molecular Cell · doi:10.1016/j.molcel.2015.08.012 · Cited by 160
Self-citationTakao, M., Kanno, S., Shiromoto, T., Hasegawa, R., Ide, H., Ikeda, S., Sarker, A. H., Seki, S., Xing, J. Z., Le, X. C., et al. (2002) · The EMBO Journal · doi:10.1093/emboj/cdf350 · Cited by 154
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Rademakers, S., Volker, M., Hoogstraten, D., Nigg, A. L., Moné, M. J., van Zeeland, A. A., Hoeijmakers, J. H. J., Houtsmuller, A. B., & Vermeulen, W. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.16.5755-5767.2003 · Cited by 149
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Lainé, J., & Egly, J. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7600933 · Cited by 152
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Self-citationDantuma, N. P., Heinen, C., & Hoogstraten, D. (2009) · DNA repair · doi:10.1016/j.dnarep.2009.01.005 · Cited by 145
Shimizu, Y., Iwai, S., Hanaoka, F., & Sugasawa, K. (2002) · The EMBO Journal · doi:10.1093/emboj/cdg016 · Cited by 142
Self-citationBasourakos, S. P., Li, L., Aparicio, A. M., Corn, P. G., Kim, J., & Thompson, T. C. (2016) · Current Medicinal Chemistry · doi:10.2174/0929867323666161214114948 · Cited by 136
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Baker, D., Wuenschell, G. E., Xia, L., Termini, J. S., Bates, S., Riggs, A. D., & O'Connor, T. R. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m702856200 · Cited by 126
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Hoogstraten, D., Bergink, S., Ng, J. M. Y., Verbiest, V. H. M., Luijsterburg, M. S., Geverts, B., Raams, A., Dinant, C., Hoeijmakers, J. H. J., Vermeulen, W., et al. (2008) · Journal of Cell Science · doi:10.1242/jcs.031708 · Cited by 122
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Thoma, B. S., & Vasquez, K. M. (2003) · Molecular Carcinogenesis · doi:10.1002/mc.10143 · Cited by 122
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Jiang, Y., Wang, X., Bao, S., Guo, R., Johnson, D. G., Shen, X., & Li, L. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1008388107 · Cited by 113
Ohkumo, T., Kondo, Y., Yokoi, M., Tsukamoto, T., Yamada, A., Sugimoto, T., Kanao, R., Higashi, Y., Kondoh, H., Tatematsu, M., et al. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.01076-06 · Cited by 111
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Self-citationSidorenko, V. S., Yeo, J.-E., Bonala, R., Johnson, F., Schärer, O. D., & Grollman, A. P. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr1095 · Cited by 107
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Janićijević, A., Sugasawa, K., Shimizu, Y., Hanaoka, F., Wijgers, N., Djurica, M., Hoeijmakers, J. H. J., & Wyman, C. (2003) · DNA repair · doi:10.1016/s1568-7864(02)00222-7 · Cited by 107
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Reynolds, M., Peterson, E., Quievryn, G., & Zhitkovich, A. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m402486200 · Cited by 105
Wang, Q.-E., Zhu, Q., Wani, G., Chen, J., & Wani, A. A. (2004) · Carcinogenesis · doi:10.1093/carcin/bgh085 · Cited by 104
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Mocquet, V., Kropachev, K. Y., Kolbanovskiy, M., Kolbanovskiy, A., Tapias, A., Cai, Y., Broyde, S. B., Geacintov, N. E., & Egly, J. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601730 · Cited by 102
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Sancar, A., & Reardon, J. T. (2004) · Advances in protein chemistry · doi:10.1016/s0065-3233(04)69002-4 · Cited by 105
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Sugasawa, K. (2009) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2009.08.004 · Cited by 102
Self-citationDNA Quality Control by Conformational Readout on the Undamaged Strand of the Double Helix
Buterin, T., Meyer, C., Giese, B., & Naegeli, H. (2005) · Chemistry & Biology · doi:10.1016/j.chembiol.2005.06.011 · Cited by 98
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Bikle, D. D. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-46227-7_14 · Cited by 96
Wang, Q. (2003) · DNA repair · doi:10.1016/s1568-7864(03)00002-8 · Cited by 97
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Chen, X., Velmurugu, Y., Zheng, G., Park, B., Shim, Y., Kim, Y., Liu, L., Houten, B. V., He, C., Ansari, A., et al. (2015) · Nature Communications · doi:10.1038/ncomms6849 · Cited by 94
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Mathieu, N., Kaczmarek, N., & Naegeli, H. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1004339107 · Cited by 97
Mathieu, N., Kaczmarek, N., Rüthemann, P., Luch, A., & Naegeli, H. (2013) · Current Biology · doi:10.1016/j.cub.2012.12.032 · Cited by 92
Cannistraro, V. J., & Taylor, J. (2009) · Journal of Molecular Biology · doi:10.1016/j.jmb.2009.07.048 · Cited by 91
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Tudek, B., Zdżalik-Bielecka, D., Tudek, A., Kosicki, K., Fabisiewicz, A., & Speina, E. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.11.043 · Cited by 93
Dissection of the Molecular Defects Caused by Pathogenic Mutations in the DNA Repair Factor XPC
de Jesus, B. B., Bjørås, M., Coin, F., & Egly, J. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.00781-08 · Cited by 89
On the relevance of hydroxyl radical to purine DNA damage
Chatgilialoglu, C., Ferreri, C., Krokidis, M. G., Masi, A., & Terzidis, M. A. (2021) · Free Radical Research · doi:10.1080/10715762.2021.1876855 · Cited by 94
Ray, A., Milum, K., Battu, A., Wani, G., & Wani, A. A. (2013) · DNA Repair · doi:10.1016/j.dnarep.2013.01.003 · Cited by 85
“In turn, XPC helps in recruiting XPA, XPG, and TFIIH components that enable opening of the DNA helix around the damage site to form a bubble [8].”
BackgroundBlockage of RNA Polymerase II at a Cyclobutane Pyrimidine Dimer and 6-4 Photoproduct
Mei Kwei, J. S., Kuraoka, I., Horibata, K., Ubukata, M., Kobatake, E., Iwai, S., Handa, H., & Tanaka, K. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.06.066 · Cited by 82
Self-citationBiochemical and Structural Domain Analysis of Xeroderma Pigmentosum Complementation Group C Protein
Bunick, C. G., Miller, M. R., Fuller, B. E., Fanning, E., & Chazin, W. (2006) · Biochemistry · doi:10.1021/bi061370o · Cited by 88
Uchida, A., Sugasawa, K., Masutani, C., Dohmae, N., Araki, M., Yokoi, M., Ohkuma, Y., & Hanaoka, F. (2002) · DNA repair · doi:10.1016/s1568-7864(02)00031-9 · Cited by 84
Self-citationXeroderma pigmentosum genes: Functions inside and outside DNA repair
Sugasawa, K. (2007) · Carcinogenesis · doi:10.1093/carcin/bgm282 · Cited by 83
Self-citationLesion recognition by XPC, TFIIH and XPA in DNA excision repair
Kim, J., Li, C., Chen, X., Cui, Y., Gołębiowski, F., Wang, H., Hanaoka, F., Sugasawa, K., & Yang, W. (2023) · Nature · doi:10.1038/s41586-023-05959-z · Cited by 90
Self-citationMolecular Anatomy of the Human Excision Nuclease Assembled at Sites of DNA Damage
Reardon, J. T., & Sancar, A. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.16.5938-5945.2002 · Cited by 81
UV-DDB-dependent regulation of nucleotide excision repair kinetics in living cells
Nishi, R., Alekseev, S., Dinant, C., Hoogstraten, D., Houtsmuller, A. B., Hoeijmakers, J. H. J., Vermeulen, W., Hanaoka, F., & Sugasawa, K. (2009) · DNA Repair · doi:10.1016/j.dnarep.2009.02.004 · Cited by 76
Self-citationCornetta, T., Festa, F., Testa, A., & Cozzi, R. (2006) · International Journal of Radiation Oncology*Biology*Physics · doi:10.1016/j.ijrobp.2006.06.037 · Cited by 80
Plosky, B. S., Samson, L. D., Engelward, B. P., Gold, B. I., Schlaen, B., Millas, T., Magnotti, M., Schor, J., & Scicchitano, D. A. (2002) · DNA repair · doi:10.1016/s1568-7864(02)00075-7 · Cited by 75
Kropachev, K. Y., Ding, S., Terzidis, M. A., Masi, A., Liu, Z., Cai, Y., Kolbanovskiy, M., Chatgilialoglu, C., Broyde, S. B., Geacintov, N. E., et al. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku162 · Cited by 77
Metadata
- Authors
- Sugasawa, K., Okamoto, T., Shimizu, Y., Masutani, C., Iwai, S., & Hanaoka, F.
- Affiliations
- Japan Science and Technology Agency (JP)
- ORCID
- Venue
- Genes & Development
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2001-03-01
- Volume
- 15
- Issue
- 5
- Pages
- 507-521
- ISSN
- 0890-9369 (ISSN-L)
- 1549-5477
- PMC
- PMC312644
- OpenAlex
- W2106443150
- Cited by
- 435
- References
- 61
- Citations by year
- 2026: 10 · 2025: 10 · 2024: 4 · 2023: 14 · 2022: 8 · 2021: 12 · 2020: 12 · 2019: 14 · 2018: 12 · 2017: 18 · 2016: 30 · 2015: 26 · 2014: 16 · 2013: 17 · 2012: 20
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Genes & Development (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Japan Science and Technology Corporation (CREST)
- RIKEN
- Core Research for Evolutional Science and Technology
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA and Nucleic Acid Chemistry
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Carcinogens and Genotoxicity Assessment
- Keywords
- nucleotide excision repair, DNA damage recognition, helix distortion, cyclobutane pyrimidine dimers
- MeSH terms
- Deoxyribonuclease I, DNA Damage, DNA Repair, DNA-Binding Proteins, Humans, Models, Biological, Nucleic Acid Conformation, Plasmids, Protein Binding, Pyrimidine Dimers, Tumor Cells, Cultured, Genome, Human, DNA Footprinting, Base Pair Mismatch
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