The DOI matches its Crossref record; 51 of the 52 references it cites were found in a registry or an index.
A Global Map of p53 Transcription-Factor Binding Sites in the Human Genome
Open accessAbstract
The ability to derive a whole-genome map of transcription-factor binding sites (TFBS) is crucial for elucidating gene regulatory networks. Herein, we describe a robust approach that couples chromatin immunoprecipitation (ChIP) with the paired-end ditag (PET) sequencing strategy for unbiased and precise global localization of TFBS. We have applied this strategy to map p53 targets in the human genome. From a saturated sampling of over half a million PET sequences, we characterized 65,572 unique p53 ChIP DNA fragments and established overlapping PET clusters as a readout to define p53 binding loci with remarkable specificity. Based on this information, we refined the consensus p53 binding motif, identified at least 542 binding loci with high confidence, discovered 98 previously unidentified p53 target genes that were implicated in novel aspects of p53 functions, and showed their clinical relevance to p53-dependent tumorigenesis in primary cancer samples.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Recent genome-wide analyses have identified from one hundred16 up to thousands17 of potential p53 target genes.”
From Census and evaluation of p53 target genes (2017) · cites this paper as [16]
Citations
Cites
WAF1, a potential mediator of p53 tumor suppression
El-Deiry, W. S., Tokino, T., Velculescu, V. E., Levy, D. B., Parsons, R., Trent, J. M., Lin, D., Mercer, W. E., Kinzler, K. W., & Vogelstein, B. (1993) · Cell · doi:10.1016/0092-8674(93)90500-p · Cited by 8,321
Genome sequencing in microfabricated high-density picolitre reactors
Margulies, M., Egholm, M., Altman, W. E., Attiya, S., Bader, J. S., Bemben, L. A., Berka, J., Braverman, M. S., Chen, Y.-J., Chen, Z., et al. (2005) · Nature · doi:10.1038/nature03959 · Cited by 7,693
Vogelstein, B., Lane, D., & Levine, A. J. (2000) · Nature · doi:10.1038/35042675 · Cited by 6,607 · cited 3×
“, 2004) or are well-known p53 targets (Polyak et al., 1997; Vogelstein et al., 2000).”
BackgroundInfluentialFinishing the euchromatic sequence of the human genome
International Human Genome Sequencing Consortium (2004) · Nature · doi:10.1038/nature03001 · Cited by 4,971
Core Transcriptional Regulatory Circuitry in Human Embryonic Stem Cells
Boyer, L. A., Lee, T. I., Cole, M. F., Johnstone, S. E., Levine, S. S., Zucker, J. P., Guenther, M. G., Kumar, R. M., Murray, H. L., Jenner, R. G., et al. (2005) · Cell · doi:10.1016/j.cell.2005.08.020 · Cited by 4,505
Capturing Chromosome Conformation
Dekker, J., Rippe, K., Dekker, M., & Kleckner, N. (2002) · Science · doi:10.1126/science.1067799 · Cited by 3,652
A model for p53-induced apoptosis
Polyak, K., Xia, Y., Zweier, J. L., Kinzler, K. W., & Vogelstein, B. (1997) · Nature · doi:10.1038/38525 · Cited by 2,500
The ENCODE (ENCyclopedia Of DNA Elements) Project
(2004) · Science · doi:10.1126/science.1105136 · Cited by 2,390
Definition of a consensus binding site for p53
El-Deiry, W. S., Kern, S. E., Pietenpol, J. A., Kinzler, K. W., & Vogelstein, B. (1992) · Nature Genetics · doi:10.1038/ng0492-45 · Cited by 1,985
Genome-Wide Location and Function of DNA Binding Proteins
Ren, B., Robert, F., Wyrick, J. J., Aparicio, O. M., Jennings, E. G., Simon, I., Zeitlinger, J., Schreiber, J., Hannett, N. M., Kanin, E. I., et al. (2000) · Science · doi:10.1126/science.290.5500.2306 · Cited by 1,768
Flagged first, then by citations
1 of the 52 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- Kuznetsov, 2005, Mathematical Analysis and Modeling of SAGE Transcriptome, 139
Cited by
Sorted by citations
Items 301–400 of 999
Wang, Z.-X., Teh, C. H.-L., Kueh, J. L. L., Lufkin, T., Robson, P., & Stanton, L. W. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m611814200 · Cited by 79
A mutant p53/let-7i-axis-regulated gene network drives cell migration, invasion and metastasis
Subramanian, M., Francis, P., Bilke, S., Li, X. L., Hara, T., Lu, X., Jones, M. F., Walker, R. L., Zhu, Y. J., Pineda, M. A., et al. (2014) · Oncogene · doi:10.1038/onc.2014.46 · Cited by 79
Garg, M., Kanojia, D., Khosla, A., Dudha, N., Sati, S., Chaurasiya, D., Jagadish, N., Seth, A., Kumar, R., Gupta, S. K., et al. (2008) · Cancer Research · doi:10.1158/0008-5472.can-08-1708 · Cited by 78
p53 Inhibits Angiogenesis by Inducing the Production of Arresten
Assadian, S., El-Assaad, W., Wang, X. Q. D., Gannon, P. O., Barrès, V., Latour, M., Mes‐Masson, A., Fred Saad, C., Sado, Y., Dostie, J., et al. (2012) · Cancer Research · doi:10.1158/0008-5472.can-11-2348 · Cited by 81
Zhou, X., Updegraff, B. L., Guo, Y., Peyton, M., Girard, L., Larsen, J. E., Xie, X., Zhou, Y., Hwang, T. H., Xie, Y., et al. (2016) · Cancer Research · doi:10.1158/0008-5472.can-16-1267-t · Cited by 75
FAK overexpression and p53 mutations are highly correlated in human breast cancer
Golubovskaya, V., Conway‐Dorsey, K., Edmiston, S. N., Tse, C., Lark, A. A., Livasy, C., Moore, D., Millikan, R. C., & Cance, W. G. (2009) · International Journal of Cancer · doi:10.1002/ijc.24486 · Cited by 77
Sun, X., Dyson, H. J., & Wright, P. E. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2021456118 · Cited by 80
In vitro analysis of DNA–protein interactions by proximity ligation
Gustafsdottir, S., Schlingemann, J., Rada-Iglesias, Á., Schallmeiner, E., Kamali‐Moghaddam, M., Wadelius, C., & Landegren, U. D. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611229104 · Cited by 78
ChIPping away at gene regulation
Massie, C. E., & Mills, I. G. (2008) · EMBO Reports · doi:10.1038/embor.2008.44 · Cited by 80
Ameri, K., Hammond, E. M., Culmsee, C., Raida, M., Katschinski, D. M., Wenger, R. H., Wagner, E., Davis, R. J., Hai, T., Denko, N. C., et al. (2006) · Oncogene · doi:10.1038/sj.onc.1209781 · Cited by 78
Diversification of caldesmon-linked actin cytoskeleton in cell motility
Mayanagi, T., & Sobue, K. (2011) · Cell Adhesion & Migration · doi:10.4161/cam.5.2.14398 · Cited by 77
Sperm-Associated Antigen 9, a Novel Biomarker for Early Detection of Breast Cancer
Kanojia, D., Garg, M., Gupta, S. K., Gupta, A., & Suri, A. (2009) · Cancer Epidemiology Biomarkers & Prevention · doi:10.1158/1055-9965.epi-08-0629 · Cited by 77
Heisig, J., Weber, D., Englberger, E., Winkler, A., Kneitz, S., Sung, W.-K. K., Wolf, E., Eilers, M., Chia-Lin, W., & Gessler, M. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002728 · Cited by 77
Self-citationDrosophila Heat Shock System as a General Model to Investigate Transcriptional RegulationPreprint
Guertin, M. J., Petesch, S. J., Zobeck, K. L., Min, I. M., & Lis, J. T. (2010) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2010.75.039 · Cited by 76
Conservation of DNA-binding specificity and oligomerisation properties within the p53 family
Brandt, T., Petrovich, M., Joerger, A. C., & Veprintsev, D. B. (2009) · BMC Genomics · doi:10.1186/1471-2164-10-628 · Cited by 77
TP53 regulates miRNA association with AGO2 to remodel the miRNA–mRNA interaction networkPreprint
Krell, J., Stebbing, J., Carissimi, C., Dabrowska, A. F., de Giorgio, A., Frampton, A. E., Harding, V., Fulci, V., Macino, G., Colombo, T., et al. (2015) · Genome Research · doi:10.1101/gr.191759.115 · Cited by 77
Dishevelled has a YAP nuclear export function in a tumor suppressor context-dependent manner
Lee, Y., Kim, N. H., Cho, E. S., Yang, J. H., Cha, Y. H., Kang, H. E., Yun, J. S., Cho, S. B., Lee, S.-H., Paclíková, P., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-04757-w · Cited by 74
Self-citationBLIMP1 regulates cell growth through repression of p53 transcription
Yan, J., Jiang, J., Lim, C. A., Wu, Q., Ng, H., & Chin, K.-C. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0605562104 · Cited by 75
Self-citationMitochondrial uncoupling reveals a novel therapeutic opportunity for p53-defective cancers
Kumar, R., Coronel, L., Somalanka, B., Raju, A., Aning, O. A., An, Ö., Ho, Y. S., Chen, S., Mak, S. Y., Hor, P. Y., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-05805-1 · Cited by 75
LncRNAs in DNA damage response and repair in cancer cells
Su, M., Wang, H., Wang, W., Wang, Y., Ouyang, L., Chen, P., Xia, L., Cao, D., & Liao, Q. (2018) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmy022 · Cited by 72
Wang, S. M. (2006) · Trends in Genetics · doi:10.1016/j.tig.2006.11.001 · Cited by 74
Katoh (2009) · International Journal of Oncology · doi:10.3892/ijo_00000514 · Cited by 76
Eldar, A., Rozenberg, H., Diskin‐Posner, Y., Rohs, R., & Shakked, Z. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt630 · Cited by 77
Lee, J. Y., Park, K., Kim, H. S., Kim, H. S., Yoo, K. H., Jung, K. S., Hong, M. E., Hong, M., Do, I., Ahn, T., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.6192 · Cited by 72
Whole-genome cartography of p53 response elements ranked on transactivation potential
Tebaldi, T., Zaccara, S., Alessandrini, F., Bisio, A., Ciribilli, Y., & Inga, A. (2015) · BMC Genomics · doi:10.1186/s12864-015-1643-9 · Cited by 72
Brázdová, M., Quante, T., Tögel, L., Walter, K., Loscher, C., Tichý, V., Činčárová, L., Deppert, W., & Tolstonog, G. V. (2009) · Nucleic Acids Research · doi:10.1093/nar/gkn1085 · Cited by 72
Hyperproliferation, cancer, and inflammation in mice expressing a Δ133p53-like isoform
Slatter, T. L., Hung, N. A., Campbell, H. G., Rubio, C., Mehta, R., Renshaw, P., Williams, G., Wilson, M., Engelmann, A., Jeffs, A. R., et al. (2011) · Blood · doi:10.1182/blood-2010-11-321851 · Cited by 76
Chang, H., Huang, H., Huang, T., Yang, P., Wang, Y., & Juan, H. (2012) · Cancer Research · doi:10.1158/0008-5472.can-12-0567 · Cited by 72
Gene Expression Profiling of Breast Cancer Brain Metastasis
Lee, J. Y., Park, K., Lee, E., Ahn, T., Jung, H. H., Lim, S. H., Hong, M. E., Do, I., Cho, E. Y., Kim, D., et al. (2016) · Scientific Reports · doi:10.1038/srep28623 · Cited by 74
A Comprehensive and High-Resolution Genome-wide Response of p53 to Stress
Chang, G. S., Chen, X. A., Park, B., Rhee, H. S., Li, P., Han, K. H., Mishra, T., Chan-Salis, K. Y., Li, Y., Hardison, R. C., et al. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.06.030 · Cited by 73
Emerging Roles of p53 Related lncRNAs in Cancer Progression: A Systematic Review
Lin, T., Hou, P., Meng, S., Chen, F., Jiang, T., Li, M.-L., Shi, M., Liu, J.-J., Zheng, J., & Bai, J. (2019) · International Journal of Biological Sciences · doi:10.7150/ijbs.33218 · Cited by 71
Self-citationExtensive Post-translational Modification of Active and Inactivated Forms of Endogenous p53
DeHart, C. J., Chahal, J. S., Flint, S. J., & Perlman, D. H. (2014) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m113.030254 · Cited by 70
SKA3 Promotes tumor growth by regulating CDK2/P53 phosphorylation in hepatocellular carcinoma
Hou, Y., Wang, Z., Huang, S., Sun, C., Zhao, J., Shi, J., Li, Z., Wang, Z., He, X., Tam, N. L., et al. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-2163-3 · Cited by 70
DNA–protein interaction studies: a historical and comparative analysis
Ferraz, R., Lopes, A. L., Silva, J., Moreira, D., Ferreira, M. J., & Coimbra, S. (2021) · Plant Methods · doi:10.1186/s13007-021-00780-z · Cited by 70
Tu, Y., Wu, W., Wu, T., Cao, Z., Wilkins, R. J., Toh, B. H., Cooper, M. E., & Chai, Z. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m609623200 · Cited by 70
Detection of a MicroRNA Signal in an In Vivo Expression Set of mRNAs
Liu, T., Papagiannakopoulos, T. Y., Puskar, K., Qi, S., Santiago, F. E., Clay, W., Lao, K., Lee, Y., Nelson, S. F., Kornblum, H. I., et al. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000804 · Cited by 69
Self-citationIdentification of TRIM22 as a RING finger E3 ubiquitin ligase
Duan, Z., Gao, B., Xu, W., & Xiong, S. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.07.070 · Cited by 70
Next generation sequencing based approaches to epigenomics
Hirst, M., & Marra, M. A. (2010) · Briefings in Functional Genomics · doi:10.1093/bfgp/elq035 · Cited by 70
Ji, H., Vokes, S. A., & Wong, W. H. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl803 · Cited by 69
Tanaka, Y., Nakamura, A., Morioka, M. S., Inoue, S., Tamamori‐Adachi, M., Yamada, K., Taketani, K., Kawauchi, J., Tanaka, M., Miyoshi, J., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0026848 · Cited by 69
Garg, M., Chaurasiya, D., Rana, R., Jagadish, N., Kanojia, D., Dudha, N., Kamran, N., Salhan, S., Bhatnagar, A., Suri, S., et al. (2007) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-06-2340 · Cited by 69
Cheok, C. F., Dey, A., & Lane, D. P. (2007) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-07-0161 · Cited by 69
Hünten, S., Kaller, M., Drepper, F., Oeljeklaus, S., Bonfert, T., Erhard, F., Dueck, A., Eichner, N., Friedel, C. C., Meister, G., et al. (2015) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m115.050237 · Cited by 70
Reversible Dysfunction of Wild-Type p53 following Homeodomain-Interacting Protein Kinase-2 Knockdown
Puca, R., Nardinocchi, L., Gal, H., Rechavi, G., Amariglio, N., Domany, E., Notterman, D. A., Scarsella, M., Leonetti, C., Sacchi, A., et al. (2008) · Cancer Research · doi:10.1158/0008-5472.can-07-6776 · Cited by 69
Pregnancy, preeclampsia and maternal aging: From epidemiology to functional genomics
Miller, E. C., Wilczek, A., Bello, N. A., Tom, S. E., Wapner, R. J., & Suh, Y. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101535 · Cited by 78
Focal adhesion kinase and p53 signal transduction pathways in cancer
Vita, M. G. (2010) · Frontiers in bioscience · doi:10.2741/3653 · Cited by 67
Tamaki, Y., Iwanaga, Y., Niizuma, S., Kawashima, T., Kato, T., Inuzuka, Y., Horie, T., Morooka, H., Takase, T., Akahashi, Y., et al. (2013) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2013.01.007 · Cited by 68
Functional evolution of the p53 regulatory network through its target response elements
Jegga, A. G., Inga, A., Menéndez, D., Aronow, B. J., & Resnick, M. A. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0704694105 · Cited by 67
Mitochondrial dysfunction induces SESN 2 gene expression through Activating Transcription Factor 4
Garaeva, A. A., Kovaleva, I. E., Chumakov, P. M., & Evstafieva, A. G. (2016) · Cell Cycle · doi:10.1080/15384101.2015.1120929 · Cited by 69
Cen, B., Lang, J. D., Du, Y., Wei, J., Xiong, Y., Bradley, N., Wang, D., & DuBois, R. N. (2019) · Gastroenterology · doi:10.1053/j.gastro.2019.11.013 · Cited by 71
Mapping the chromosomal targets of STAT1 by Sequence Tag Analysis of Genomic Enrichment (STAGE)Preprint
Bhinge, A., Kim, J., Euskirchen, G. M., Snyder, M. P., & Iyer, V. R. (2007) · Genome Research · doi:10.1101/gr.5574907 · Cited by 67
Maslon, M. M., & Hupp, T. R. (2010) · Trends in Cell Biology · doi:10.1016/j.tcb.2010.06.005 · Cited by 68
Methylation and deamination of CpGs generate p53-binding sites on a genomic scale
Żemojtel, T., Kiełbasa, S. M., Arndt, P. F., Chung, H., & Vingron, M. (2008) · Trends in Genetics · doi:10.1016/j.tig.2008.11.005 · Cited by 66
Functional Analysis of p53 Binding under Differential Stresses
Krieg, A. J., Hammond, E. M., & Giaccia, A. J. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.00322-06 · Cited by 65
Gallegos, J. E., & Rose, A. B. (2019) · Scientific Reports · doi:10.1038/s41598-019-50389-5 · Cited by 65
Updates on p53: modulation of p53 degradation as a therapeutic approach
Dey, A., Verma, C. S., & Lane, D. P. (2008) · British Journal of Cancer · doi:10.1038/sj.bjc.6604098 · Cited by 65
Menéndez, D., Inga, A., Snipe, J. R., Krysiak, O., Schönfelder, G., & Resnick, M. A. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.01742-06 · Cited by 68
Zhao, B., Shah, P., Budanov, A. V., Qiang, L., Ming, M., Aplin, A., Sims, D. M., & He, Y.-Y. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.595397 · Cited by 61
The p53/microRNA Network in Cancer: Experimental and Bioinformatics Approaches
Hünten, S., Siemens, H., Kaller, M., & Hermeking, H. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-94-007-5590-1_5 · Cited by 66
Liu, D., Perkins, J. T., Petriello, M. C., & Hennig, B. (2015) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2015.10.015 · Cited by 65
Kobayashi, M., Takahashi, E., Miyagawa, S., Watanabe, H., & Iguchi, T. (2006) · Genes to Cells · doi:10.1111/j.1365-2443.2006.01009.x · Cited by 65
hCLCA2 Is a p53-Inducible Inhibitor of Breast Cancer Cell Proliferation
Walia, V., Ding, M., Kumar, S., Nie, D., Premkumar, L. S., & Elble, R. C. (2009) · Cancer Research · doi:10.1158/0008-5472.can-08-4101 · Cited by 66
Fischer, M., Grundke, I., Sohr, S., Quaas, M., Hoffmann, S., Knörck, A., Gumhold, C., & Rother, K. (2013) · PLoS ONE · doi:10.1371/journal.pone.0063187 · Cited by 64
p53 inactivation by MDM2 and MDMX negative feedback loops in testicular germ cell tumors
Li, B., Cheng, Q., Li, Z., & Chen, J. (2010) · Cell Cycle · doi:10.4161/cc.9.7.11255 · Cited by 64
Wang, B., Feng, P., Xiao, Z., & Ren, E.-C. (2008) · Journal of Hepatology · doi:10.1016/j.jhep.2008.10.025 · Cited by 66
Khazanov, N., & Levy, Y. (2011) · Journal of Molecular Biology · doi:10.1016/j.jmb.2011.01.059 · Cited by 65
AATF/Che‐1 acts as a phosphorylation‐dependent molecular modulator to repress p53‐driven apoptosis
Höpker, K., Hagmann, H., Khurshid, S., Chen, S., Hasskamp, P., Seeger‐Nukpezah, T., Schilberg, K., Heukamp, L. C., Lamkemeyer, T., Sos, M. L., et al. (2012) · The EMBO Journal · doi:10.1038/emboj.2012.236 · Cited by 64
CLEAN: CLustering Enrichment ANalysis
Freudenberg, J., Joshi, V. K., Hu, Z., & Medvedovic, M. (2009) · BMC Bioinformatics · doi:10.1186/1471-2105-10-234 · Cited by 64
Feedbacks, Bifurcations, and Cell Fate Decision-Making in the p53 System
Hat, B., Kochańczyk, M., Bogdał, M. N., & Tomasz Lipniacki, B. (2016) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004787 · Cited by 65
Puumalainen, M.-R., Rüthemann, P., Min, J., & Naegeli, H. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-2075-z · Cited by 71
Duale, N., Lindeman, B., Komada, M., Olsen, A.-K. H., Andreassen, Å. K., Søderlund, E. J., & Brunborg, G. (2007) · Molecular Cancer · doi:10.1186/1476-4598-6-53 · Cited by 63
Systematic functional characterization ofcis-regulatory motifs in human core promotersPreprint
Sinha, S., Adler, A. S., Field, Y., Chang, H. Y., & Segal, E. (2008) · Genome Research · doi:10.1101/gr.6828808 · Cited by 62
CerS6 Is a Novel Transcriptional Target of p53 Protein Activated by Non-genotoxic Stress
Fekry, B., Jeffries, K. A., Esmaeilniakooshkghazi, A., Ogretmen, B., Krupenko, S. A., & Krupenko, N. I. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.716902 · Cited by 59
Induction of genetic instability by gain-of-function p53 cancer mutants
Xu, Y. (2008) · Oncogene · doi:10.1038/sj.onc.1211023 · Cited by 63
Fischer, M., Quaas, M., Wintsche, A., Müller, G. A., & Engeland, K. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt849 · Cited by 66
Nadal, E., Chen, G., Gallegos, M., Lin, L., Ferrer-Torres, D., Truini, A., Wang, Z., Lin, J., Reddy, R. M., Llatjós, R., et al. (2013) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-13-0736 · Cited by 62
Subtelomeric p53 binding prevents accumulation of DNA damage at human telomeres
Tutton, S., Azzam, G. A., Stong, N., Vladimirova, O. V., Wiedmer, A., Monteith, J., Beishline, K., Wang, Z., Deng, Z., Riethman, H. C., et al. (2015) · The EMBO Journal · doi:10.15252/embj.201490880 · Cited by 69
Animal Models to Study MicroRNA Function
Pal, A. S., & Kasinski, A. L. (2017) · Advances in cancer research · doi:10.1016/bs.acr.2017.06.006 · Cited by 64
Hyter, S., Coleman, D. J., Ganguli‐Indra, G., Merrill, G. F., Ma, S., Yanagisawa, M., & Indra, A. K. (2013) · Pigment Cell & Melanoma Research · doi:10.1111/pcmr.12063 · Cited by 61
The p53 Pathway and Metabolism: The Tree That Hides the Forest
Lahalle, A., Lacroix, M., Blasio, C. D., Cissé, M. Y., Linares, L. K., & Cam, L. L. (2021) · Cancers · doi:10.3390/cancers13010133 · Cited by 69
αB‐crystallin: A novel p53‐target gene required for p53‐dependent apoptosis
Watanabe, G., Kato, S., Nakata, H., Ishida, T., Ohuchi, N., & Ishioka, C. (2009) · Cancer Science · doi:10.1111/j.1349-7006.2009.01316.x · Cited by 61
Weilbacher, A., Gutekunst, M., Oren, M., Aulitzky, W. E., & van der Kuip, H. (2014) · Cell Death and Disease · doi:10.1038/cddis.2014.284 · Cited by 62
Phenotype Specific Analyses Reveal Distinct Regulatory Mechanism for Chronically Activated p53
Kirschner, K., Samarajiwa, S., Cairns, J., Menon, S., Pérez-Mancera, P. A., Tomimatsu, K., Bermejo‐Rodríguez, C., Ito, Y., Chandra, T., Narita, M., et al. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005053 · Cited by 61
Gutekunst, M., Mueller, T., Weilbacher, A., Dengler, M. A., Bedke, J., Kruck, S., Oren, M., Aulitzky, W. E., & van der Kuip, H. (2013) · Cancer Research · doi:10.1158/0008-5472.can-12-2876 · Cited by 61
Ribosomal Protein S27-like, a p53-Inducible Modulator of Cell Fate in Response to Genotoxic Stress
Li, J., Tan, J. Y., Li, Z., Banerjee, B., Yang, X., Chau, J. F. L., Lee, P. L., Hande, M. P., Li, B., & Yu, Q. (2007) · Cancer Research · doi:10.1158/0008-5472.can-07-1088 · Cited by 60
Self-citationOhki, R., Kawase, T., Ohta, T., Ichikawa, H., & Taya, Y. (2006) · Cancer Science · doi:10.1111/j.1349-7006.2006.00375.x · Cited by 64
High-Throughput Methods of Regulatory Element Discovery
Hudson, M. E., & Snyder, M. P. (2006) · BioTechniques · doi:10.2144/000112322 · Cited by 60
The next generation: Using new sequencing technologies to analyse gene regulation
Cullum, R., Alder, O., & Hoodless, P. A. (2010) · Respirology · doi:10.1111/j.1440-1843.2010.01899.x · Cited by 61
Rap2b, a novel p53 target, regulates p53-mediated pro-survival function
Zhang, X., He, Y., Lee, K. H., Dubois, W., Li, Z., Wu, X., Kovalchuk, A. L., Zhang, W., & Huang, J. L. (2013) · Cell Cycle · doi:10.4161/cc.24364 · Cited by 59
SPATA18, a Spermatogenesis-Associated Gene, Is a Novel Transcriptional Target of p53 and p63
Bornstein, C., Brosh, R., Molchadsky, A., Madar, S., Kogan-Sakin, I., Goldstein, I., Chakravarti, D., Flores, E. R., Goldfinger, N., Sarig, R., et al. (2011) · Molecular and Cellular Biology · doi:10.1128/mcb.01072-10 · Cited by 63
Rossi, M., Demidov, O. N., Anderson, C. W., Appella, E., & Mazur, S. J. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn888 · Cited by 57
Argininosuccinate synthase 1 is an intrinsic Akt repressor transactivated by p53
Miyamoto, T., Lo, P. H. Y., Saichi, N., Ueda, K., Hirata, M., Tanikawa, C., & Matsuda, K. (2017) · Science Advances · doi:10.1126/sciadv.1603204 · Cited by 60
DNA binding by FOXP3 domain-swapped dimer suggests mechanisms of long-range chromosomal interactions
Chen, Y., Chen, C., Zhang, Z., Liu, C.-C., Johnson, M. E., Espinoza, C. A., Edsall, L., Ren, B., Zhou, X. J., Grant, S. F. A., et al. (2015) · Nucleic Acids Research · doi:10.1093/nar/gku1373 · Cited by 59
Visnagri, A., Kandhare, A. D., Ghosh, P., & Bodhankar, S. L. (2013) · Cardiovascular Endocrinology · doi:10.1097/xce.0000000000000010 · Cited by 58
Agarwal, S. K., Impey, S., McWeeney, S. K., Scacheri, P. C., Collins, F. S., Goodman, R. H., Spiegel, A. M., & Marx, S. J. (2007) · Neoplasia · doi:10.1593/neo.06706 · Cited by 59
p53 induces distinct epigenetic states at its direct target promoters
Vrba, L., Junk, D. J., Novák, P., & Futscher, B. W. (2008) · BMC Genomics · doi:10.1186/1471-2164-9-486 · Cited by 60
P53 transcriptional activities: A general overview and some thoughts
Millau, J., Bastien, N., & Drouin, R. (2008) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2008.06.002 · Cited by 65
p53-Dependent Transcriptional Control of Cellular Prion by Presenilins
Vincent, B., Sunyach, C., Orzechowski, H., George‐Hyslop, P. S., & Checler, F. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0789-09.2009 · Cited by 62
Targeting the Ubiquitin-Mediated Proteasome Degradation of p53 for Cancer Therapy
DeVine, T., & Dai, M. (2013) · Current Pharmaceutical Design · doi:10.2174/1381612811319180009 · Cited by 58
Expression signatures of TP53 mutations in serous ovarian cancers
Bernardini, M. Q., Baba, T., Lee, P. S., Barnett, J. C., Sfakianos, G. P., Secord, A. A., Murphy, S. K., Iversen, E. S., Marks, J. R., & Berchuck, A. (2010) · BMC Cancer · doi:10.1186/1471-2407-10-237 · Cited by 56
Metadata
- Authors
- Wei, C.-L., Wu, Q., Vega, V. B., Chiu, K. P., Ng, P., Zhang, T., Shahab, A., Yong, H. C., Fu, Y., Weng, Z., Liu, J., Zhao, X. D., Chew, J.-L., Lee, Y. L., Kuznetsov, V. A., Sung, W.-K., Miller, L. D., Lim, B., Liu, E. T., Yu, Q., Ng, H.-H., & Ruan, Y.
- Affiliations
- Genome Institute of Singapore (SG)
- Bioinformatics Institute (SG)
- Boston University (US)
- National University of Singapore (SG)
- Harvard University (US)
- Corresponding author
- Ng, Huck-Hui
- Ruan, Yijun
- ORCID
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2006-01
- Volume
- 124
- Issue
- 1
- Pages
- 207-219
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W2171407623
- Cited by
- 1,141
- References
- 52
- Citations by year
- 2026: 7 · 2025: 14 · 2024: 11 · 2023: 29 · 2022: 38 · 2021: 30 · 2020: 25 · 2019: 32 · 2018: 38 · 2017: 39 · 2016: 56 · 2015: 43 · 2014: 57 · 2013: 61 · 2012: 66
- FWCI
- 56.35
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 2790 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- National University of Singapore (submittedVersion)
- Funders
- Genome Institute of Singapore
- National Institutes of Health (8r01hg000352-03)
- National Human Genome Research Institute (1R01HG00352-01)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
- Keywords
- p53, transcription factor binding sites, ChIP-seq, p53 target genes, gene regulatory networks, cancer, human genome
- MeSH terms
- Binding Sites, Chromosome Mapping, DNA, Humans, Transcription Factors, Tumor Cells, Cultured, Genome, Human, Tumor Suppressor Protein p53, Oligonucleotide Array Sequence Analysis, HCT116 Cells, Chromatin Immunoprecipitation
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