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Purification and cloning of a nucleotide excision repair complex involving the xeroderma pigmentosum group C protein and a human homologue of yeast RAD23.
Open accessAbstract
Complementation group C of xeroderma pigmentosum (XP) represents one of the most common forms of this cancer-prone DNA repair syndrome. The primary defect is located in the subpathway of the nucleotide excision repair system, dealing with the removal of lesions from the non-transcribing sequences ('genome-overall' repair). Here we report the purification to homogeneity and subsequent cDNA cloning of a repair complex by in vitro complementation of the XP-C defect in a cell-free repair system containing UV-damaged SV40 minichromosomes. The complex has a high affinity for ssDNA and consists of two tightly associated proteins of 125 and 58 kDa. The 125 kDa subunit is an N-terminally extended version of previously reported XPCC gene product which is thought to represent the human homologue of the Saccharomyces cerevisiae repair gene RAD4. The 58 kDa species turned out to be a human homologue of yeast RAD23. Unexpectedly, a second human counterpart of RAD23 was identified. All RAD23 derivatives share a ubiquitin-like N-terminus. The nature of the XP-C defect implies that the complex exerts a unique function in the genome-overall repair pathway which is important for prevention of skin cancer.
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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 [230]
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“Both hHR23A and -B harbor a ubiquitin-like moiety at their amino terminus [230].”
From Molecular Mechanisms of Ultraviolet Radiation‐Induced DNA Damage and Repair (2010) · cites this paper as [230]
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Citations
Cites
Bradford, M. M. (1976) · Analytical Biochemistry · doi:10.1016/0003-2697(76)90527-3 · Cited by 255,302
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
LAEMMLI, U. K. (1970) · Nature · doi:10.1038/227680a0 · Cited by 249,961
Basic local alignment search tool
Altschul, S. F., Gish, W., Miller, W., Myers, E. W., & Lipman, D. J. (1990) · Journal of Molecular Biology · doi:10.1006/jmbi.1990.9999 · Cited by 98,669
Molecular cloning: A laboratory manual
Deininger, P. L. (1990) · Analytical Biochemistry · doi:10.1016/0003-2697(90)90595-z · Cited by 84,684
DNA sequencing with chain-terminating inhibitors
Sanger, F., Nicklen, S., & Coulson, A. R. (1977) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.74.12.5463 · Cited by 68,572
Raza, H., John, A., & Nemmar, A. (2013) · Cellular Physiology and Biochemistry · doi:10.1159/000350087 · Cited by 47,311
Structural features in eukaryotic mRNAs that modulate the initiation of translation.
Kozak, M. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)54860-2 · Cited by 1,826
Defective repair replication of DNA in xeroderma pigmentosum
CLEAVER, J. E. (1968) · Nature · doi:10.1038/218652a0 · Cited by 1,729
λ ZAP: a bacteriophage λ expression vector within vivoexcision properties
Short, J. M., Fernandez, J. M., Sorge, J. A., & Huse, W. D. (1988) · Nucleic Acids Research · doi:10.1093/nar/16.15.7583 · Cited by 1,365
Kraemer, K. H. (1987) · Archives of Dermatology · doi:10.1001/archderm.123.2.241 · Cited by 1,216
Research works printed but not linked: 7
- Bailly,V., Sommers,C.H., Sung,P., Prakash,L. and Prakash,S. (1992) Proc. Natl Acad. Sci. USA, 89, 8273 -8277.
- Baneri,J., Sands,J., Strominger,J.L. and Spies,T. (1990) Proc. NatlAcad. Sci. USA, 87, 2374-2378.
- Flejter,W.L., McDaniel,L.D., Johns,D., Friedberg,E.C. and Schultz,R.A. (1992) Proc. Natl Acad. Sci. USA, 89, 261 -265.
- Huang,J.-C., Svoboda,D.L., Reardon,J.T. and Sancar,A. (1992) Proc. Natl Acad. Sci. USA, 89, 3664-3668.
- Koken,M.H.M., Reynolds,P., Jaspers-Dekker,I., Prakash,L., Prakash,S., Bootsma,D. and Hoeijmakers,J.H.J. (1991) Proc. NatlAcad. Sci. USA, 88, 8865-8869.
- Sanger,F., Nicklen,S. and Coulson,A.R. (1977) Proc. NatlAcad. Sci. USA, 74, 5463-5467.
- Toniolo,D., Persico,M. and Alcalay,M. (1988) Proc. NatlAcad. Sci. USA, 85, 851-855.
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Items 201–300 of 400
Zhu, Q., Wani, G., Wani, M. A., & Wani, A. A. (2001) · PubMed · Cited by 41
Mechanisms of DNA damage recognition in mammalian nucleotide excision repair
Naegeli, H. (1995) · The FASEB Journal · doi:10.1096/fasebj.9.11.7649403 · Cited by 41
Multiple DNA damage recognition factors involved in mammalian nucleotide excision repair
Sugasawa, K. (2011) · Biochemistry (Moscow) · doi:10.1134/s0006297911010044 · Cited by 44
Self-citationCharacterization and expression of a rice RAD23 gene
Schultz, T. F., & Quatrano, R. S. (1997) · Plant Molecular Biology · doi:10.1023/a:1005870227632 · Cited by 40
Dong, Z., Guo, W., Zhou, R., Lingling, W., Li, Y., Wang, N., Kuang, G., & Wang, S. (2008) · Journal of Clinical Gastroenterology · doi:10.1097/mcg.0b013e3180f6262c · Cited by 39
Structure of the XPC binding domain of hHR23A reveals hydrophobic patches for protein interaction
Kamionka, M., & Feigon, J. F. (2004) · Protein Science · doi:10.1110/ps.04824304 · Cited by 40
Two isoforms of plant RAD23 complement a UV‐sensitive rad23 mutant in yeast
Sturm, A., & Lienhard, S. (1998) · The Plant Journal · doi:10.1046/j.1365-313x.1998.00075.x · Cited by 38
Gururaja, T. L., Li, W., Noble, W. S., Payan, D. G., & Anderson, D. C. (2003) · Journal of Proteome Research · doi:10.1021/pr034019n · Cited by 38
Bergink, S., Severijnen, L.-A. W. F. M., Wijgers, N., Sugasawa, K., Yousaf, H., Kros, J. M., Swieten, J. C. V., Oostra, B. A., Hoeijmakers, J. H. J., Vermeulen, W., et al. (2006) · Neurobiology of Disease · doi:10.1016/j.nbd.2006.06.005 · Cited by 38
Self-citationHistone H4K20 Demethylation by Two hHR23 Proteins
Cao, X., Chen, Y., Wu, B., Wang, X., Xue, H., Yu, L., Li, J., Wang, Y., Wang, W., Xu, Q., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.03.001 · Cited by 37
The involvement of XPC protein in the cisplatin DNA damaging treatment-mediated cellular response
Gan, W. A. N. G., Dombkowski, A. A., CHUANG, L., & XU, X. X. S. (2004) · Cell Research · doi:10.1038/sj.cr.7290375 · Cited by 35
RetractedMa, L., Siemssen, E. D., Noteborn, M. H. M., & van der Eb, A. J. (1994) · Nucleic Acids Research · doi:10.1093/nar/22.20.4095 · Cited by 37
A role for Rad23 proteins in 26S proteasome-dependent protein degradation?
van Laar, T., van der Eb, A. J., & Terleth, C. (2002) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(01)00291-3 · Cited by 37
XPC: Its Product and Biological Roles
Sugasawa, K. (2008) · Advances in Experimental Medicine and Biology · doi:10.1007/978-0-387-09599-8_6 · Cited by 36
Self-citationImmune and inflammatory responses to DNA damage in cancer and aging
Soria‐Valles, C., López‐Soto, A., Osorio, F. G., & López-Otín, C. (2016) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2016.10.004 · Cited by 36
Verhage, R. A., Zeeman, A., Lombaerts, M., van de Putte, P., & Brouwer, J. (1996) · Mutation Research/DNA Repair · doi:10.1016/0921-8777(95)00045-3 · Cited by 36
Araki, M., Masutani, C., Maekawa, T., Watanabe, Y., Yamada, A., Kusumoto, R., Sakai, D., Sugasawa, K., Ohkuma, Y., & Hanaoka, F. (2000) · Mutation Research/DNA Repair · doi:10.1016/s0921-8777(99)00067-1 · Cited by 35
Self-citationTwo mammalian homologs of yeast Rad23, HR23A and HR23B, as multifunctional proteins
Yokoi, M., & Hanaoka, F. (2016) · Gene · doi:10.1016/j.gene.2016.10.027 · Cited by 34
XPC beyond nucleotide excision repair and skin cancers
Zebian, A., Shaito, A. A., Mazurier, F., Rezvani, H. R., & Zibara, K. (2019) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2019.108286 · Cited by 36
Cells From Long-Lived Mutant Mice Exhibit Enhanced Repair of Ultraviolet Lesions
Salmon, A. B., Ljungman, M. E., & Miller, R. A. (2008) · The Journals of Gerontology Series A · doi:10.1093/gerona/63.3.219 · Cited by 36
Mechanism and regulation of DNA damage recognition in mammalian nucleotide excision repair
Sugasawa, K. (2019) · The Enzymes · doi:10.1016/bs.enz.2019.06.004 · Cited by 33
Self-citationAntiviral immunity and nucleic acid sensing in haematopoietic stem cell gene engineering
Piras, F., & Kajaste‐Rudnitski, A. (2020) · Gene Therapy · doi:10.1038/s41434-020-0175-3 · Cited by 32
Maillard, O., Camenisch, U., Blagoev, K. B., & Naegeli, H. (2008) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2008.01.007 · Cited by 36
Shimizu, Y., Uchimura, Y., Dohmae, N., Saitoh, H., Hanaoka, F., & Sugasawa, K. (2010) · Journal of Nucleic Acids · doi:10.4061/2010/805698 · Cited by 33
Self-citationFrancis, M. A., & Rainbow, A. J. (1999) · Carcinogenesis · doi:10.1093/carcin/20.1.19 · Cited by 33
Sequence of the mouse XPC cDNA and genomic structure of the human XPC gene
Li, L. (1996) · Nucleic Acids Research · doi:10.1093/nar/24.6.1026 · Cited by 33
Architecture of the human XPC DNA repair and stem cell coactivator complex
Zhang, E., He, Y., Grob, P., Fong, Y. W., Nogales, E., & Tjian, R. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1520104112 · Cited by 31
Regulation of UV-induced DNA damage response by ubiquitylation
Bergink, S., Jaspers, N. G. J., & Vermeulen, W. (2007) · DNA repair · doi:10.1016/j.dnarep.2007.01.012 · Cited by 33
Orchestral maneuvers at the damaged sites in nucleotide excision repair
Alekseev, S., & Coin, F. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-1859-5 · Cited by 36
Mechanism of action of nucleotide excision repair machinery
D'Souza, A., Blee, A. M., & Chazin, W. (2022) · Biochemical Society Transactions · doi:10.1042/bst20210246 · Cited by 36
Gaynor, E. M., & Chen, I. S. Y. (2001) · Experimental Cell Research · doi:10.1006/excr.2001.5247 · Cited by 31
The moonlighting of RAD23 in DNA repair and protein degradation
Grønbæk-Thygesen, M., Kampmeyer, C., Hofmann, K., & Hartmann‐Petersen, R. (2023) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2023.194925 · Cited by 31
Associations betweenXPC expression, genotype, and the risk of head and neck cancer
Yang, M., Kang, M.-J., Choi, Y., Kim, C.-S., Lee, S.-M., Park, C.-W., Lee, H.-S., & Tae, K. (2005) · Environmental and Molecular Mutagenesis · doi:10.1002/em.20097 · Cited by 30
Nucleosome Unfolding during DNA Repair in Normal and Xeroderma Pigmentosum (Group C) Human Cells
Baxter, B. K., & Smerdon, M. J. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.28.17517 · Cited by 30
Sakai, W., Yuasa‐Sunagawa, M., Kusakabe, M., Kishimoto, A., Matsui, T., Kaneko, Y., Akagi, J., Huyghe, N. D., Ikura, M., Ikura, T., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-76898-2 · Cited by 30
Self-citationLi, J., Tian, L., Jing, Z., Guo, Z., Nan, P., Liu, F., Zou, S., Yang, L., Xie, X., Zhu, Y., et al. (2021) · Cancer Letters · doi:10.1016/j.canlet.2021.05.033 · Cited by 29
Timing of DNA lesion recognition: Ubiquitin signaling in the NER pathway
Chitale, S., & Richly, H. (2016) · Cell Cycle · doi:10.1080/15384101.2016.1261227 · Cited by 32
XPC–PARP complexes engage the chromatin remodeler ALC1 to catalyze global genome DNA damage repair
Blessing, C., Apelt, K., van den Heuvel, D., Gonzalez-Leal, C., Rother, M. B., van der Woude, M., González‐Prieto, R., Yifrach, A., Parnas, A., Shah, R. G., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-31820-4 · Cited by 30
Slor, H., Batko, S., Khan, S. G., Sobe, T., Emmert, S., Khadavi, A., Frumkin, A., Busch, D. B., Albert, R. B., & Kraemer, K. H. (2000) · Journal of Investigative Dermatology · doi:10.1046/j.1523-1747.2000.00190.x · Cited by 28
Bhatia, P. K., Wang, Z., & Friedberg, E. C. (1996) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(96)80043-8 · Cited by 28
Kang, S., Sun, H., Zhou, R., Wang, N., Hu, P., & Li, Y. (2013) · Asian Pacific Journal of Cancer Prevention · doi:10.7314/apjcp.2013.14.2.941 · Cited by 27
Seroz, T. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.22.4506 · Cited by 27
Cancer Predisposition in Mutant Mice Defective in the XPC DNA Repair Gene
Friedberg, E. C., Cheo, D. L., Meira, L. B., & dos Reis, A. M. (1999) · KARGER eBooks · doi:10.1159/000062011 · Cited by 26
Bae, D. (2003) · Toxicological Sciences · doi:10.1093/toxsci/kfg124 · Cited by 26
Extrachromosomal recombination occurs efficiently in cells defective in various DNA repair systems
Morrison, C. G. (1996) · Nucleic Acids Research · doi:10.1093/nar/24.11.2053 · Cited by 26
Shimamoto, T., Tanimura, T., Yoneda, Y., Kobayakawa, Y., Sugasawa, K., Hanaoka, F., Oka, M., Okada, Y., Tanaka, K., & Kohno, K. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.38.22452 · Cited by 25
Self-citationPickart, C. M. (1998) · Springer eBooks · doi:10.1007/978-1-4899-1922-9_2 · Cited by 26
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
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
McKay, B. C., & Rainbow, A. J. (1996) · Mutation Research/DNA Repair · doi:10.1016/0921-8777(96)00013-4 · Cited by 23
Nucleotide excision repair in yeast
Sweder, K. (1994) · Current Genetics · doi:10.1007/bf00326572 · Cited by 22
Brois, D. W., McMahon, L., Ramos, N. I., Anglin, L. M., Walsh, C., & Lambert, M. W. (1999) · Carcinogenesis · doi:10.1093/carcin/20.9.1845 · Cited by 21
Fousteri, M. I., & Lehmann, A. R. (2003) · CRC Press eBooks · doi:10.1201/9780203911709.ch17 · Cited by 21
Other Proteins Interacting with XP Proteins
Shell, S. M., & Zou, Y. (2008) · Advances in experimental medicine and biology · doi:10.1007/978-0-387-09599-8_11 · Cited by 21
Iwai, S., Mizukoshi, T., Fujiwara, Y., Masutani, C., Hanaoka, F., & Hayakawa, Y. (1999) · Nucleic Acids Research · doi:10.1093/nar/27.11.2299 · Cited by 20
Self-citationJowett, J. B. M., Xie, Y., & Chen, I. S. Y. (1999) · Journal of Virology · doi:10.1128/jvi.73.9.7132-7137.1999 · Cited by 20
Rauh‐Adelmann, C., Lau, K., Sabeti, N., Long, J. P., Mok, S. C., & Ho, S. (2000) · Molecular Carcinogenesis · doi:10.1002/1098-2744(200008)28:4 · Cited by 48
Quantification of XPA gene expression levels in human and mouse cell lines by competitive RT-PCR
Layher, S. K., & Cleaver, J. E. (1997) · Mutation Research/DNA Repair · doi:10.1016/s0921-8777(96)00040-7 · Cited by 19
Tramutola, A., Falcucci, S., Brocco, U., Triani, F., Lanzillotta, C., Donati, M., Panetta, C., Luzi, F., Iavarone, F., Vincenzoni, F., et al. (2020) · Cancers · doi:10.3390/cancers12010110 · Cited by 19
den Dulk, B., Brandsma, J. A., & Brouwer, J. (2005) · Molecular Microbiology · doi:10.1111/j.1365-2958.2005.04607.x · Cited by 18
Identification and Characterization of the rhp23+ DNA Repair Gene in Schizosaccharomyces pombe
Lombaerts, M., Goeloe, J. I., den Dulk, H., Brandsma, J. A., & Brouwer, J. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.2100 · Cited by 18
Hess, N. J., Buchko, G. W., Ni, S., Thrall, B. D., Kennedy, M. A., Conradson, S. D., & Espinosa-Faller, F. J. (1998) · Protein Science · doi:10.1002/pro.5560070912 · Cited by 18
Gene expression changes associated with cytotoxicity identified using cDNA arrays
Gore, M. A., Morshedi, M. M., & Reidhaar-Olson, J. F. (2000) · Functional & Integrative Genomics · doi:10.1007/s101420000015 · Cited by 17
DNA damage-induced inflammation and nuclear architecture
Stratigi, K., Chatzidoukaki, O., & Garinis, G. A. (2016) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2016.09.008 · Cited by 17
Ikehata, H., Kaneda, S., Yamao, F., Seno, T., Ono, T., & Hanaoka, F. (1997) · Molecular and Cellular Biology · doi:10.1128/mcb.17.3.1484 · Cited by 16
Lechner, S. M., Müller‐Ladner, U., Neumann, E., Dietmaier, W., Welsh, J., Schölmerich, J., Rüschoff, J., & Kullmann, F. (2001) · Laboratory Investigation · doi:10.1038/labinvest.3780337 · Cited by 16
Kim, B., Ryu, K., Kim, H., Cho, S., & Choi, B. (2005) · FEBS Journal · doi:10.1111/j.1742-4658.2005.04667.x · Cited by 15
Proteins that participate in nucleotide excision repair of DNA in mammalian cells
Wood, R. D. (1995) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.1995.0011 · Cited by 15
Protein-protein interactions in the core nucleotide excision repair pathway
D’Souza, A., Kim, M., Chazin, W., & Schärer, O. D. (2024) · DNA repair · doi:10.1016/j.dnarep.2024.103728 · Cited by 16
Nucleotide Excision Repair and Response and Survival to Chemotherapy in Colorectal Cancer Patients
Kap, E. J., Popanda, O., & Chang-Claude, J. C. (2016) · Pharmacogenomics · doi:10.2217/pgs-2015-0017 · Cited by 14
Detection of bulky DNA lesions: DDB2 at the interface of chromatin and DNA repair in eukaryotes
Jones, K. L., Zhang, L., Seldeen, K. L., & Gong, F. (2010) · IUBMB Life · doi:10.1002/iub.391 · Cited by 14
Hsieh, H.-C., Hsieh, Y., Huang, Y.-H., Shen, F.-C., Tsai, H.-N., Tsai, J.-H., Lai, Y.-T., Wang, Y.-T., Chuang, W., & Huang, W. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.07.067 · Cited by 14
Molecular Mechanism of Nucleotide Excision Repair in Mammalian Cells
Reardon, J. T., & Sancar, A. (1999) · Springer eBooks · doi:10.1007/978-1-4615-4865-2_31 · Cited by 14
Jessberger, R. (1997) · Nucleic Acids Research · doi:10.1093/nar/25.2.289 · Cited by 14
Ultraviolet Radiation Carcinogenesis
Cleaver, J. E., Ortiz‐Urda, S., Gulhar, R., Arron, S. T., Brookes, L., & Mitchell, D. L. (2017) · Wiley eBooks · doi:10.1002/9781119000822.hfcm026 · Cited by 14
Wang, N., Gong, X., & Ma, F. (2017) · Journal of Integrative Agriculture · doi:10.1016/s2095-3119(16)61517-4 · Cited by 13
Lysine deserts prevent adventitious ubiquitylation of ubiquitin-proteasome components
Kampmeyer, C., Grønbæk-Thygesen, M., Oelerich, N., Tatham, M. H., Cagiada, M., Lindorff‐Larsen, K., Boomsma, W., Hofmann, K., & Hartmann‐Petersen, R. (2023) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-023-04782-z · Cited by 13
DNA Repair and Chromatin Structure in Genetic Diseases
Lambert, M. W., & Lambert, W. C. (1999) · Progress in nucleic acid research and molecular biology · doi:10.1016/s0079-6603(08)60725-4 · Cited by 13
Kino, K., Shimizu, Y., Sugasawa, K., Sugiyama, H., & Hanaoka, F. (2004) · Biochemistry · doi:10.1021/bi0361416 · Cited by 13
Self-citationPapel das proteínas XPD e DNA polimerase eta nas respostas de células humanas a danos no genoma
Lerner, L. K. (2014) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2014.tde-20102014-103732 · Cited by 13
Mori, M. P. (2015) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.46.2015.tde-20072015-105008 · Cited by 13
Emerging Roles of Post-Translational Modifications in Nucleotide Excision Repair
Borsos, B. N., Majoros, H., & Pankotai, T. (2020) · Cells · doi:10.3390/cells9061466 · Cited by 12
Miron, S. M., Duchambon, P., Blouquit, Y., Christiane, D. D., & Craescu, C. T. (2008) · Biochemistry · doi:10.1021/bi701863u · Cited by 12
Fukumoto, Y., Hiyama, H., Yokoi, M., Nakaseko, Y., Yanagida, M., & Hanaoka, F. (2002) · DNA repair · doi:10.1016/s1568-7864(02)00108-8 · Cited by 12
Saccharomyces cerevisiae DNA repair processes: an update
Ramotar, D., & Masson, J. (1996) · Molecular and Cellular Biochemistry · doi:10.1007/bf00225884 · Cited by 12
Tada, S., Yanagisawa, J., Sonoyama, T., Miyajima, A., Seki, M., Ui, M., & Enomoto, T. (1996) · Cell Structure and Function · doi:10.1247/csf.21.123 · Cited by 12
Self-citationButler, R. M., McKenzie, R. C. T., Jones, C. L., Flanagan, C. E., Woollard, W. J., Demontis, M. A., Ferreira, S., Tosi, I., John, S., Whittaker, S. J., et al. (2019) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2019.03.1130 · Cited by 11
Enhancing protein stability with retained biological function in transgenic plants
Jang, I., Niu, Q., Deng, S., Zhao, P., & Chua, N. (2012) · The Plant Journal · doi:10.1111/j.1365-313x.2012.05060.x · Cited by 11
Jung, J., Byeon, I. L., DeLucia, M., Koharudin, L. M. I., Ahn, J., & Gronenborn, A. M. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.534453 · Cited by 11
Chicheva, Z., Chelenkova, P., Petkova, R., & Chakarov, S. (2012) · Biotechnology & Biotechnological Equipment · doi:10.5504/bbeq.2012.0052 · Cited by 11
Okuda, M., Tsunaka, Y., & Nishimura, Y. (2022) · Biophysical Reviews · doi:10.1007/s12551-022-01014-9 · Cited by 10
Role of some epigenetic factors in DNA damage response pathway
Tiwari, M., Parvez, S., & Agrawala, P. K. (2017) · Global Medical Genetics · doi:10.3934/genet.2017.1.69 · Cited by 10
Zebian, A., Dor, M. E., Shaito, A. A., Mazurier, F., Rezvani, H. R., & Zibara, K. (2021) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2021.108400 · Cited by 10
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Metadata
- Authors
- Masutani, C., Sugasawa, K., Yanagisawa, J., Sonoyama, T., Ui, M., Enomoto, T., Takio, K., Tanaka, K., van der Spek, P. J., & Bootsma, D.
- Affiliations
- RIKEN (JP)
- Venue
- The EMBO Journal
- Published
- 1994-04-01
- Volume
- 13
- Issue
- 8
- Pages
- 1831-1843
- ISSN
- 0261-4189 (ISSN-L)
- 1460-2075
- PMC
- PMC395023
- OpenAlex
- W1005028082
- Cited by
- 400
- References
- 70
- Citations by year
- 2026: 5 · 2025: 2 · 2024: 6 · 2023: 6 · 2022: 5 · 2021: 7 · 2020: 8 · 2019: 9 · 2018: 5 · 2017: 7 · 2016: 13 · 2015: 9 · 2014: 7 · 2013: 5 · 2012: 9
- FWCI
- 9.75
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- The EMBO Journal (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
- Funders
- Cosmetology Research Foundation
- RIKEN
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nuclear Structure and Function
- Keywords
- xeroderma pigmentosum group C, nucleotide excision repair, Rad23, Rad4, UV-damaged DNA, single-stranded DNA binding, cDNA cloning, protein complex purification, skin cancer prevention, SV40 minichromosomes
- MeSH terms
- Amino Acid Sequence, Base Sequence, DNA Damage, DNA Repair, DNA-Binding Proteins, DNA, Viral, Fungal Proteins, HeLa Cells, Humans, Models, Molecular, Molecular Sequence Data, Transglutaminases, Simian virus 40, Ubiquitins, Ultraviolet Rays, Sequence Homology, Amino Acid, DNA, Complementary, Schizosaccharomyces pombe Proteins, DNA Repair Enzymes
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