The DOI matches its Crossref record; 56 of the 56 references it cites were found in a registry or an index.
RAD26, the functional S. cerevisiae homolog of the Cockayne syndrome B gene ERCC6.
Open accessAbstract
Transcription-coupled repair (TCR) is a universal sub-pathway of the nucleotide excision repair (NER) system that is limited to the transcribed strand of active structural genes. It accomplishes the preferential elimination of transcription-blocking DNA lesions and permits rapid resumption of the vital process of transcription. A defect in TCR is responsible for the rare hereditary disorder Cockayne syndrome (CS). Recently we found that mutations in the ERCC6 repair gene, encoding a putative helicase, underly the repair defect of CS complementation group B. Here we report the cloning and characterization of the Saccharomyces cerevisiae homolog of CSB/ERCC6, which we designate RAD26. A rad26 disruption mutant appears viable and grows normally, indicating that the gene does not have an essential function. In analogy with CS, preferential repair of UV-induced cyclobutane pyrimidine dimers in the transcribed strand of the active RBP2 gene is severely impaired. Surprisingly, in contrast to the human CS mutant, yeast RAD26 disruption does not induce any UV-, cisPt- or X-ray sensitivity, explaining why it was not isolated as a mutant before. Recovery of growth after UV exposure was somewhat delayed in rad26. These findings suggest that TCR in lower eukaryotes is not very important for cell survival and that the global genome repair pathway of NER is the major determinant of cellular resistance to genotoxicity.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The text we found for this paper looks like another document, so the self-check wasn’t run.
Citations
Cites
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
Multiple sequence alignment with hierarchical clustering.
Corpet, F. (1988) · Nucleic Acids Research · doi:10.1093/nar/16.22.10881 · Cited by 5,575
How eukaryotic transcriptional activators work
Ptashne, M. (1988) · Nature · doi:10.1038/335683a0 · Cited by 1,828
Robbins, J., Dilwortht, S. M., Laskey, R. A., & Dingwall, C. (1991) · Cell · doi:10.1016/0092-8674(91)90245-t · Cited by 1,490
MELLON, I. (1987) · Cell · doi:10.1016/0092-8674(87)90151-6 · Cited by 1,228
Tamkun, J. W., Deuring, R., Scott, M. P., Kissinger, M., Pattatucci, A. M. L., Kaufman, T. C., & Kennison, J. A. (1992) · Cell · doi:10.1016/0092-8674(92)90191-e · Cited by 988
Sancar, A., & Sancar, G. B. (1988) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.57.070188.000333 · Cited by 815
Cockayne syndrome: Review of 140 cases
Nance, M. A., & Berry, S. A. (1992) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320420115 · Cited by 806
DNA 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
Self-citation
Cited by
Sorted by citations
Items 101–200 of 244
Clever, B., Schmuckli‐Maurer, J., Sigrist, M., Glassner, B. J., & Heyer, W. (1999) · Yeast · doi:10.1002/(sici)1097-0061(19990630)15:9 · Cited by 40
Orren, D. K. (1996) · Nucleic Acids Research · doi:10.1093/nar/24.17.3317 · Cited by 39
Jiang, H., Wolgast, M., Beebe, L. M., & Reese, J. C. (2019) · Genes & Development · doi:10.1101/gad.322453.118 · Cited by 39
Chen, X., Ruggiero, C., & Li, S. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.00404-07 · Cited by 38
Lommel, L., Bucheli, M. E., & Sweder, K. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.150130197 · Cited by 38
Tijsterman, M. (1996) · Nucleic Acids Research · doi:10.1093/nar/24.18.3499 · Cited by 38
Dorazi, R., Götz, D., Munro, S., Bernander, R., & White, M. F. (2006) · Molecular Microbiology · doi:10.1111/j.1365-2958.2006.05516.x · Cited by 39
Guzder, S. N., Prakash, L., Prakash, S., & Sung, P. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.34.24257 · Cited by 37
You, Z., Feaver, W. J., & Friedberg, E. C. (1998) · Molecular and Cellular Biology · doi:10.1128/mcb.18.5.2668 · Cited by 37
The pleiotropic roles of SPT5 in transcription
Song, A., & Chen, F. (2022) · Transcription · doi:10.1080/21541264.2022.2103366 · Cited by 36
A new connection of mRNP biogenesis and export with transcription-coupled repair
Gaillard, H., Wellinger, R. E., & Aguilera, A. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm373 · Cited by 35
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
Self-citationTatum, D. M., Li, W., Placer, M., & Li, S. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.252981 · Cited by 35
Repair of plasmid and genomic DNA in arad7Δ mutant of yeast
Mueller, J. P., & Smerdon, M. J. (1995) · Nucleic Acids Research · doi:10.1093/nar/23.17.3457 · Cited by 34
The roles of Rad16 and Rad26 in repairing repressed and actively transcribed genes in yeast
Li, S., Ding, B., LeJeune, D., Ruggiero, C., Chen, X., & Smerdon, M. J. (2007) · DNA repair · doi:10.1016/j.dnarep.2007.05.005 · Cited by 33
Interaction of the yeast Pso5/Rad16 and Sgs1 proteins: influences on DNA repair and aging
Saffi, J., Feldmann, H. M., Winnacker, E., & Henriques, J. A. P. (2001) · Mutation Research/DNA Repair · doi:10.1016/s0921-8777(01)00093-3 · Cited by 32
Rad33, a new factor involved in nucleotide excision repair in Saccharomyces cerevisae
den Dulk, B., Sun, S. M., de Ruijter, M., Brandsma, J. A., & Brouwer, J. (2006) · DNA repair · doi:10.1016/j.dnarep.2006.02.002 · Cited by 32
Self-citationLi, S., Ding, B., Chen, R., Ruggiero, C., & Chen, X. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.01656-06 · Cited by 31
Nucleotide excision repair in chromatin: Damage removal at the drop of a HAT
Reed, S. H. (2011) · DNA repair · doi:10.1016/j.dnarep.2011.04.029 · Cited by 30
den Dulk, B., van Eijk, P., de Ruijter, M., Brandsma, J. A., & Brouwer, J. (2008) · DNA repair · doi:10.1016/j.dnarep.2008.02.004 · Cited by 30
Self-citationLi, W., Selvam, K., Rahman, S. A., & Li, S. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw428 · Cited by 29
Reed, S. H., Waters, R., & Boiteux, S. (1996) · Molecular and General Genetics MGG · doi:10.1007/bf02174039 · Cited by 29
Transcription factor IIS impacts UV-inhibited transcription
Jensen, A., & Mullenders, L. H. F. (2010) · DNA repair · doi:10.1016/j.dnarep.2010.08.002 · Cited by 28
Lombaerts, M. (1997) · Nucleic Acids Research · doi:10.1093/nar/25.20.3974 · 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
Svensson, J. P., Pesudo, L. Q., Fry, R. C., Adeleye, Y. A., Carmichael, P. L., & Samson, L. D. (2011) · BMC Systems Biology · doi:10.1186/1752-0509-5-157 · Cited by 26
Yeast Elc1 plays an important role in global genomic repair but not in transcription coupled repair
LeJeune, D., Chen, X., Ruggiero, C., Berryhill, S., Ding, B., & Li, S. (2008) · DNA repair · doi:10.1016/j.dnarep.2008.08.010 · Cited by 27
Yasuhira, S., Yasui, A., & Morimyo, M. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.38.26822 · Cited by 26
Nucleotide excision repair in chromatin: The shape of things to come
Reed, S. H. (2005) · DNA repair · doi:10.1016/j.dnarep.2005.04.009 · Cited by 27
Rad26p regulates the occupancy of histone H2A–H2B dimer at the active genes in vivo
Malik, S., Chaurasia, P., Lahudkar, S., Uprety, B., & Bhaumik, S. R. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr1244 · Cited by 26
Lee, M., Ahn, B., Choi, I. S., & Koo, H. (2002) · FEBS Letters · doi:10.1016/s0014-5793(02)02880-6 · 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
Tremblay, M., Teng, Y., Paquette, M., Waters, R., & Conconi, A. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.00137-08 · Cited by 24
Aboussekhra, A., & Al-Sharif, I. S. (2005) · The EMBO Journal · doi:10.1038/sj.emboj.7600665 · Cited by 24
Goldman-Levi, R. (1996) · Nucleic Acids Research · doi:10.1093/nar/24.16.3121 · Cited by 24
Powell, N. G. (2003) · DNA repair · doi:10.1016/s1568-7864(02)00239-2 · Cited by 24
Tfb5 interacts with Tfb2 and facilitates nucleotide excision repair in yeast
Zhou, Y., Kou, H., & Wang, Z. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkl1085 · Cited by 23
Reagan, M. S., & Friedberg, E. C. (1997) · Nucleic Acids Research · doi:10.1093/nar/25.21.4257 · Cited by 23
Heidenreich, E., Holzmann, V., & Eisler, H. (2004) · DNA repair · doi:10.1016/j.dnarep.2003.12.004 · Cited by 23
Rpb1 Sumoylation in Response to UV Radiation or Transcriptional Impairment in Yeast
Chen, X., Ding, B., LeJeune, D., Ruggiero, C., & Li, S. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005267 · Cited by 23
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
Transcription elongation factor S-II is not required for transcription-coupled repair in yeast
Verhage, R. A., Heyn, J., van de Putte, P., & Brouwer, J. (1997) · Molecular and General Genetics MGG · doi:10.1007/s004380050417 · Cited by 22
Self-citationSweder, K. (1996) · Nucleic Acids Research · doi:10.1093/nar/24.8.1540 · Cited by 22
Gaillard, H., & Aguilera, A. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004203 · Cited by 20
Tilting at windmills? The nucleotide excision repair of chromosomal DNA
Waters, R., Teng, Y., Yu, Y., Yu, S., & Reed, S. H. (2008) · DNA repair · doi:10.1016/j.dnarep.2008.11.001 · Cited by 20
Repair-Independent Chromatin Assembly onto Active Ribosomal Genes in Yeast after UV Irradiation
Conconi, A., Paquette, M., Fahy, D., Bespalov, V. A., & Smerdon, M. J. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.22.9773-9783.2005 · Cited by 21
Tijsterman, M., & Brouwer, J. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.3.1199 · Cited by 22
Self-citationFukumoto, Y., Dohmae, N., & Hanaoka, F. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.00757-08 · Cited by 21
Friedberg, E. C., Feaver, W. J., Huang, W., Reagan, M. S., Reed, S. H., You, Z., Wei, S., Rodriguez, K. A., Talamantez, J. L., & Tomkinson, A. E. (1999) · Springer eBooks · doi:10.1007/978-1-4615-4865-2_10 · Cited by 20
Taschner, M., Harreman, M., Teng, Y., Gill, H., Anindya, R., Maslen, S. L., Skehel, J. M., Waters, R., & Svejstrup, J. Q. (2010) · Molecular and Cellular Biology · doi:10.1128/mcb.00822-09 · Cited by 19
Zhang, X., Xu, J., Hu, J., Zhang, S., Hao, Y., Zhang, D., Qian, H., Wang, D., & Fu, X. (2024) · Nature Communications · doi:10.1038/s41467-024-50298-w · Cited by 19
UV damage regulates alternative polyadenylation of the RPB2 gene in yeast
Yu, L., & Volkert, M. R. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt020 · Cited by 19
Khobta, A., Lingg, T., Schulz, I., Warken, D., Kitsera, N., & Epe, B. (2010) · DNA repair · doi:10.1016/j.dnarep.2010.06.011 · Cited by 19
Facilitators and Repressors of Transcription‐coupled DNA Repair in Saccharomyces cerevisiae
Li, W., & Li, S. (2016) · Photochemistry and Photobiology · doi:10.1111/php.12655 · Cited by 19
Sancar, G. B., Ferris, R. G., Smith, F. W., & Berg, B. J. V. (1995) · Nucleic Acids Research · doi:10.1093/nar/23.21.4320 · Cited by 19
Yu, S., Teng, Y., Lowndes, N. F., & Waters, R. (2001) · Mutation Research/DNA Repair · doi:10.1016/s0921-8777(01)00061-1 · Cited by 18
den Dulk, B., Brandsma, J. A., & Brouwer, J. (2005) · Molecular Microbiology · doi:10.1111/j.1365-2958.2005.04607.x · Cited by 18
Self-citationWu, X. (2001) · Nucleic Acids Research · doi:10.1093/nar/29.14.3123 · Cited by 19
Mechanism of Rad26-assisted rescue of stalled RNA polymerase II in transcription-coupled repair
Yan, C., Dodd, T., Yu, J., Leung, B., Xu, J., Oh, J., Wang, D., & Ivanov, I. N. (2021) · Nature Communications · doi:10.1038/s41467-021-27295-4 · Cited by 17
Modulation of Rad26- and Rpb9-mediated DNA Repair by Different Promoter Elements
Li, S., Chen, X., Ruggiero, C., Ding, B., & Smerdon, M. J. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m604885200 · Cited by 16
Characterization of the rhp7+ and rhp16+ genes in Schizosaccharomyces pombe
Lombaerts, M., Peltola, P., Visse, R., den Dulk, H., Brandsma, J. A., & Brouwer, J. (1999) · Nucleic Acids Research · doi:10.1093/nar/27.17.3410 · Cited by 17
Self-citationRepair of Damaged and Mismatched DNA by the XPC Homologues Rhp41 and Rhp42 of Fission Yeast
Marti, T. M., Kunz, C., & Fleck, O. (2003) · Genetics · doi:10.1093/genetics/164.2.457 · Cited by 16
Méniel, V. S., Magaña‐Schwencke, N., & Averbeck, D. (1995) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/0027-5107(95)00023-c · Cited by 16
Regulation of nucleotide excision repair through ubiquitination
Li, J., Bhat, A., & Xiao, W. (2011) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmr088 · Cited by 16
Jansen, L. E. T. (2002) · Nucleic Acids Research · doi:10.1093/nar/gkf475 · Cited by 15
Teng, Y., Yu, Y., Ferreiro, J. A., & Waters, R. (2005) · DNA repair · doi:10.1016/j.dnarep.2005.04.006 · Cited by 14
Bucheli, M. E., & Sweder, K. (2004) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04081.x · Cited by 14
Mechanisms of transcription-coupled repair and DNA damage surveillance in health and disease
van Sluis, M., Gonzalo-Hansen, C., Li, Q., Lans, H., Wang, D., & Marteijn, J. A. F. (2025) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-025-00915-3 · Cited by 21
Concannon, C., & Lahue, R. S. (2013) · DNA repair · doi:10.1016/j.dnarep.2013.11.004 · Cited by 13
Scott, A. D., & Waters, R. (1997) · Molecular and General Genetics MGG · doi:10.1007/s004380050389 · Cited by 13
Methods to Study Transcription-Coupled Repair in Chromatin
Gaillard, H., Wellinger, R. E., & Aguilera, A. (2009) · Methods in molecular biology · doi:10.1007/978-1-59745-190-1_10 · Cited by 13
Def1 interacts with TFIIH and modulates RNA polymerase II transcription
Damodaren, N., van Eeuwen, T., Zamel, J., Lin-Shiao, E., Kalisman, N., & Murakami, K. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1707955114 · Cited by 13
Halmai, M., Frittmann, O., Szabo, Z., Daraba, A., Gali, V. K., Bálint, É., & Unk, I. (2016) · PLoS ONE · doi:10.1371/journal.pone.0161307 · Cited by 13
Charton, R., Guintini, L., Peyresaubes, F., & Conconi, A. (2015) · DNA repair · doi:10.1016/j.dnarep.2015.09.007 · Cited by 12
Deaconescu, A. M., & Suhanovsky, M. M. (2016) · Photochemistry and Photobiology · doi:10.1111/php.12661 · Cited by 13
Set2 histone methyltransferase regulates transcription coupled-nucleotide excision repair in yeast
Selvam, K., Plummer, D. A., Mao, P., & Wyrick, J. J. (2022) · PLoS Genetics · doi:10.1371/journal.pgen.1010085 · Cited by 14
RNA Polymerase Signals UvrAB Landing Sites
Ahn, B., & Grossman, L. I. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.35.21453 · 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
Al-Moghrabi, N. M., Al-Sharif, I. S., & Aboussekhra, A. (2003) · DNA Repair · doi:10.1016/j.dnarep.2003.07.002 · Cited by 11
Mechanism of transcription modulation by the transcription-repair coupling factor
Paudel, B. P., Xu, Z., Jergic, S., Oakley, A. J., Sharma, N., Brown, S. H. J., Bouwer, J. C., Lewis, P. J., Dixon, N. E., van Oijen, A. M., et al. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac449 · Cited by 11
Morse, N. R. (2002) · Nucleic Acids Research · doi:10.1093/nar/30.8.1799 · Cited by 11
DNA excision repair and transcription: implications for genome evolution
Sullivan, D. (1995) · Current Opinion in Genetics & Development · doi:10.1016/0959-437x(95)80012-t · Cited by 11
Bang, D. D., Ketting, R. F., de Ruijter, M., Brandsma, J. A., Verhage, R. A., van de Putte, P., & Brouwer, J. (1996) · Mutation Research/DNA Repair · doi:10.1016/0921-8777(96)00010-9 · Cited by 11
Self-citationHan, P., Zhang, Y.-L., Ying, S., & Feng, M. (2023) · Microbiological Research · doi:10.1016/j.micres.2023.127589 · Cited by 10
Stopped in its tracks: The RNA polymerase molecular motor as a robust sensor of DNA damage
Howan, K., Monnet, J., Fan, J., & Strick, T. R. (2014) · DNA repair · doi:10.1016/j.dnarep.2014.02.018 · Cited by 10
Bucheli, M. E., Lommel, L., & Sweder, K. (2001) · Genetics · doi:10.1093/genetics/158.3.989 · Cited by 10
Nucleotide Excision Repair in S. cerevisiae
Tatum, D. M., & Li, S. (2011) · InTech eBooks · doi:10.5772/22129 · Cited by 9
DEF1: Much more than an RNA polymerase degradation factor
Akinniyi, O. T., & Reese, J. C. (2021) · DNA repair · doi:10.1016/j.dnarep.2021.103202 · Cited by 10
Chaurasia, P., Sen, R., & Bhaumik, S. R. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.413716 · Cited by 9
Open gaps in the evolution of the eukaryotic nucleotide excision repair
Feltrin, R. D. S., Segatto, A. L. A., de Souza, T. A., & Schuch, A. P. (2020) · DNA repair · doi:10.1016/j.dnarep.2020.102955 · Cited by 9
Ding, B., Ruggiero, C., Chen, X., & Li, S. (2007) · DNA repair · doi:10.1016/j.dnarep.2007.06.001 · Cited by 9
Recombination and its roles in DNA repair, cellular immortalization and cancer
Shammas, M. A., & Reis, R. J. S. (1999) · AGE · doi:10.1007/s11357-999-0009-0 · Cited by 9
RNA polymerase II depletion promotes transcription of alternative mRNA species
Yu, L., Rege, M., Peterson, C. L., & Volkert, M. R. (2016) · BMC Molecular Biology · doi:10.1186/s12867-016-0074-8 · Cited by 8
Guintini, L., Tremblay, M., Toussaint, M., D’Amours, A., Wellinger, R. E., Wellinger, R. J., & Conconi, A. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx123 · Cited by 8
Toussaint, M., Wellinger, R. J., & Conconi, A. (2010) · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · doi:10.1016/j.mrgentox.2010.03.013 · Cited by 7
Nucleotide excision repair syndromes: molecular basis and clinical symptoms
Bootsma, D., Weeda, G., Vermeulen, W., van Vuuren, H., Troelstra, C., van der Spek, P. J., & Hoeijmakers, J. H. J. (1995) · Springer eBooks · doi:10.1007/978-94-011-0537-8_11 · Cited by 7
Self-citationFrom xeroderma pigmentosum to the biological clock contributions of Dirk Bootsma to human genetics
Hoeijmakers, J. H. J. (2001) · Mutation Research/DNA Repair · doi:10.1016/s0921-8777(00)00079-3 · Cited by 7
Self-citationRoy, S. G., Das, D., Chowdhury, D., Smerdon, M. J., & Chaudhuri, R. N. (2013) · PLoS ONE · doi:10.1371/journal.pone.0072090 · Cited by 7
Metadata
- Authors
- van Gool, A. J., Verhage, R., Swagemakers, S. M., van de Putte, P., Brouwer, J., Troelstra, C., Bootsma, D., & Hoeijmakers, J. H.
- Affiliations
- Erasmus University Rotterdam (NL)
- ORCID
- Hoeijmakers, J.H.
- Venue
- The EMBO Journal
- Published
- 1994-11-01
- Volume
- 13
- Issue
- 22
- Pages
- 5361-5369
- ISSN
- 0261-4189 (ISSN-L)
- 1460-2075
- PMC
- PMC395493
- OpenAlex
- W2112652171
- Cited by
- 246
- References
- 56
- Citations by year
- 2025: 2 · 2024: 5 · 2023: 5 · 2022: 6 · 2021: 8 · 2020: 2 · 2019: 1 · 2018: 3 · 2017: 4 · 2016: 8 · 2015: 3 · 2014: 7 · 2013: 7 · 2012: 4
- FWCI
- 6.46
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- The EMBO Journal (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- RePub (Erasmus University Rotterdam) (submittedVersion, other-oa)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nuclear Structure and Function
- Keywords
- Rad26, ERCC6, Cockayne syndrome B, transcription-coupled repair, nucleotide excision repair, Saccharomyces cerevisiae, cyclobutane pyrimidine dimers, UV-induced DNA damage, RBP2, global genome repair, cisplatin sensitivity, X-ray sensitivity, helicase, gene essentiality
- MeSH terms
- Poly-ADP-Ribose Binding Proteins, Amino Acid Sequence, Cockayne Syndrome, DNA Damage, DNA Repair, DNA Helicases, DNA, Fungal, Fungal Proteins, Genes, Fungal, Humans, Molecular Sequence Data, Saccharomyces cerevisiae, Species Specificity, Transcription, Genetic, Ultraviolet Rays, Sequence Alignment, Sequence Homology, Amino Acid, Cell Cycle Proteins, Schizosaccharomyces pombe Proteins, DNA Repair Enzymes
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review