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DNA methylation patterns and epigenetic memory
Open accessAbstract
The character of a cell is defined by its constituent proteins, which are the result of specific patterns of gene expression. Crucial determinants of gene expression patterns are DNA-binding transcription factors that choose genes for transcriptional activation or repression by recognizing the sequence of DNA bases in their promoter regions. Interaction of these factors with their cognate sequences triggers a chain of events, often involving changes in the structure of chromatin, that leads to the assembly of an active transcription complex (e.g., Cosma et al. 1999). But the types of transcription factors present in a cell are not alone sufficient to define its spectrum of gene activity, as the transcriptional potential of a genome can become restricted in a stable manner during development. The constraints imposed by developmental history probably account for the very low efficiency of cloning animals from the nuclei of differentiated cells (Rideout et al. 2001; Wakayama and Yanagimachi 2001). A “transcription factors only” model would predict that the gene expression pattern of a differentiated nucleus would be completely reversible upon exposure to a new spectrum of factors. Although many aspects of expression can be reprogrammed in this way (Gurdon 1999), some marks of differentiation are evidently so stable that immersion in an alien cytoplasm cannot erase the memory. The genomic sequence of a differentiated cell is thought to be identical in most cases to that of the zygote from which it is descended (mammalian B and T cells being an obvious exception). This means that the marks of developmental history are unlikely to be caused by widespread somatic mutation. Processes less irrevocable than mutation fall under the umbrella term “epigenetic” mechanisms. A current definition of epigenetics is: “The study of mitotically and/or meiotically heritable changes in gene function that cannot be explained by changes in DNA sequence” (Russo et al. 1996). There are two epigenetic systems that affect animal development and fulfill the criterion of heritability: DNA methylation and the Polycomb-trithorax group (Pc-G/trx) protein complexes. (Histone modification has some attributes of an epigenetic process, but the issue of heritability has yet to be resolved.) This review concerns DNA methylation, focusing on the generation, inheritance, and biological significance of genomic methylation patterns in the development of mammals. Data will be discussed favoring the notion that DNA methylation may only affect genes that are already silenced by other mechanisms in the embryo. Embryonic transcription, on the other hand, may cause the exclusion of the DNA methylation machinery. The heritability of methylation states and the secondary nature of the decision to invite or exclude methylation support the idea that DNA methylation is adapted for a specific cellular memory function in development. Indeed, the possibility will be discussed that DNA methylation and Pc-G/trx may represent alternative systems of epigenetic memory that have been interchanged over evolutionary time. Animal DNA methylation has been the subject of several recent reviews (Bird and Wolffe 1999; Bestor 2000; Hsieh 2000; Costello and Plass 2001; Jones and Takai 2001). For recent reviews of plant and fungal DNA methylation, see Finnegan et al. (2000), Martienssen and Colot (2001), and Matzke et al. (2001).
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“When methylation occurs within promoter regions, transcription factors are blocked from binding and gene expression is reduced or silenced”
From The clinical use of epigenetics in psychiatry: a narrative review of epigenetic mechanisms, key candidate genes, and precision psychiatry (2025) · cites this paper as [9]
Experimental — accuracy not yet measuredIn the citing paper
“DNA itself is also subject to methylation on the C5 atom of cytosine (Bird, 2002).”
From Influence of Metabolism on Epigenetics and Disease (2013) · cites this paper as Bird, 2002
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1 retracted
Transient depletion of xDnmt1 leads to premature gene activation in Xenopus embryosPreprint
Stancheva, I., & Meehan, R. R. (2000) · Genes & Development · doi:10.1101/gad.14.3.313 · Cited by 184
RetractedInitial sequencing and analysis of the human genome
International Human Genome Sequencing Consortium, Whitehead Institute for Biomedical Research, C. F. G. R., Lander, E. S., Linton, L. M., Birren, B., Nusbaum, C., Zody, M. C., Baldwin, J., Devon, K., Dewar, K., et al. (2001) · Nature · doi:10.1038/35057062 · Cited by 24,216
The sequence of the human genome
Venter, J. C., Adams, M. D., Myers, E. W., Li, P. W., Mural, R. J., Sutton, G. G., Smith, H. O., Yandell, M., Evans, C. A., Holt, R. A., et al. (2001) · Science · doi:10.1126/science.1058040 · Cited by 13,909
Jenuwein, T., & Allis, C. D. (2001) · Science · doi:10.1126/science.1063127 · Cited by 9,756
Okano, M., Bell, D. W., Haber, D. A., & Li, E. (1999) · Cell · doi:10.1016/s0092-8674(00)81656-6 · Cited by 6,143
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
Amir, R. E., Van den Veyver, I. B., Wan, M., Tran, C. Q., Francke, U., & Zoghbi, H. Y. (1999) · Nature Genetics · doi:10.1038/13810 · Cited by 4,990
Targeted mutation of the DNA methyltransferase gene results in embryonic lethality
Li, E., Bestor, T. H., & Jaenisch, R. (1992) · Cell · doi:10.1016/0092-8674(92)90611-f · Cited by 3,984
CpG-rich islands and the function of DNA methylation
Bird, A. P. (1986) · Nature · doi:10.1038/321209a0 · Cited by 3,777
Self-citationEpigenetic Reprogramming in Mammalian Development
Reik, W., Dean, W., & Walter, J. (2001) · Science · doi:10.1126/science.1063443 · Cited by 3,078
Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain
Bannister, A. J., Zegerman, P., Partridge, J. F., Miska, E. A., Thomas, J. O., Allshire, R. C., & Kouzarides, T. (2001) · Nature · doi:10.1038/35065138 · Cited by 2,903
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- 10.1093/humrep/ · DOI
- 1981, Reactivation of an inactive human X-chromosome: Evidence for X-inactivation by DNA methylation., Science, 211, 393, 10.1126/science.6164095 · DOI
- Prokhortchouk, 2001, The p120 catenin partner Kaiso is a DNA methylation-dependent transcriptional repressor., Genes & Dev., 15, 1613, 10.1101/gad.198501 · DOI · Paper page
Cited by
Sorted by citations
Items 701–800 of 1,038
Handa, V., & Jeltsch, A. (2005) · Journal of Molecular Biology · doi:10.1016/j.jmb.2005.02.044 · Cited by 162
Chuang, J. C., Warner, S. L., Vollmer, D. L., Vankayalapati, H., Redkar, S., Bearss, D. J., Qiu, X., Yoo, C. B., & Jones, P. A. (2010) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-09-1048 · Cited by 162
Kalac, M., Scotto, L., Marchi, E., Amengual, J. E., Seshan, V., Bhagat, G., Ulahannan, N., Leshchenko, V. V., Temkin, A. M., Parekh, S. S., et al. (2011) · Blood · doi:10.1182/blood-2011-02-336891 · Cited by 161
Epigenetic regulation of normal and malignant hematopoiesis
Rice, K. L., Hormaeche, I., & Licht, J. D. (2007) · Oncogene · doi:10.1038/sj.onc.1210755 · Cited by 161
ROS3 is an RNA-binding protein required for DNA demethylation in Arabidopsis
Zheng, X., Pontes, O., Zhu, J., Miki, D., Zhang, F., Li, W.-X., Iida, K., Kapoor, A., Pikaard, C. S., & Zhu, J. (2008) · Nature · doi:10.1038/nature07305 · Cited by 161
Gene Regulatory Network Inference: An Introductory Survey
Huynh‐Thu, V. A., & Sanguinetti, G. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-8882-2_1 · Cited by 163
Exercise for osteoporosis: A literature review of pathology and mechanism
Zhang, L., Zheng, Y.-L., Wang, R., Wang, X., & Zhang, H. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1005665 · Cited by 161
Modulation of DNMT1 activity by ADP-ribose polymers
Reale, A., MATTEIS, G. D., Galleazzi, G., Zampieri, M., & Caiafa, P. (2005) · Oncogene · doi:10.1038/sj.onc.1208005 · Cited by 161
L1 (LINE-1) retrotransposon diversity differs dramatically between mammals and fish
Furano, A. V. (2003) · Trends in Genetics · doi:10.1016/j.tig.2003.11.006 · Cited by 161
Epigenetic remodelling licences adult cholangiocytes for organoid formation and liver regeneration
Aloia, L., McKie, M. A., Vernaz, G., Cordero-Espinoza, L., Aleksieva, N., van den Ameele, J., Antonica, F., Font-Cunill, B., Raven, A., Aiese Cigliano, R., et al. (2019) · Nature Cell Biology · doi:10.1038/s41556-019-0402-6 · Cited by 160
Hidalgo, B., Irvin, M. R., Sha, J., Zhi, D., Aslibekyan, S., Absher, D., Tiwari, H. K., Kabagambe, E. K., Ordovas, J. M., & Arnett, D. K. (2014) · Diabetes · doi:10.2337/db13-1100 · Cited by 160
Epigenetic regulation of endometrium during the menstrual cycle
Munro, S. K., Farquhar, C. M., Mitchell, M. D., & Ponnampalam, A. P. (2010) · Molecular Human Reproduction · doi:10.1093/molehr/gaq010 · Cited by 160
Dynamic and static maintenance of epigenetic memory in pluripotent and somatic cells
Shipony, Z., Mukamel, Z., Cohen, N. M., Landan, G., Chomsky, E., Zeliger, S. R., Fried, Y. C., Ainbinder, E., Friedman, N., & Tanay, A. (2014) · Nature · doi:10.1038/nature13458 · Cited by 159
Sproul, D., Nestor, C., Culley, J., Dickson, J. H., Dixon, J. M., Harrison, D. J., Meehan, R. R., Sims, A. H., & Ramsahoye, B. H. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1013224108 · Cited by 159
Kozlenkov, A., Roussos, P., Timashpolsky, A., Barbu, M., Rudchenko, S., Bibikova, M. V., Klotzle, B., Byne, W. M., Lyddon, R., Narzo, A. F. D., et al. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt838 · Cited by 159
DNA methylation and microRNA biomarkers for noninvasive detection of gastric and colorectal cancer
Toiyama, Y., Okugawa, Y., & Goel, A. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.08.001 · Cited by 159
Epigenetic regulation in cancer progression
Baxter, E., Windloch, K., Gannon, F., & Lee, J. S. (2014) · Cell & Bioscience · doi:10.1186/2045-3701-4-45 · Cited by 159
Ming, X., Zhang, Z., Zou, Z., Lv, C., Dong, Q., He, Q., Yi, Y., Li, Y., Wang, H., & Zhu, B. (2020) · Cell Research · doi:10.1038/s41422-020-0359-9 · Cited by 159
DNA methyltransferase inhibitors: old and new drugs for an epigenetic cancer therapy
Brueckner, B., & Lyko, F. (2004) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2004.09.004 · Cited by 159
DNA methylation in the preimplantation embryo: the differing stories of the mouse and sheep
Young, L. E., & Beaujean, N. (2004) · Animal Reproduction Science · doi:10.1016/j.anireprosci.2004.05.020 · Cited by 159
Epigenomic replication: Linking epigenetics to DNA replication
McNairn, A. J., & Gilbert, D. M. (2003) · BioEssays · doi:10.1002/bies.10305 · Cited by 159
Molecular mechanism for USP7-mediated DNMT1 stabilization by acetylation.
Cheng, J., Yang, H., Fang, J., Ma, L., Gong, R., Wang, P., Li, Z., & Xu, Y. (2015) · Nature Communications · doi:10.1038/ncomms8023 · Cited by 158
Epigenetics and airways disease
Adcock, I. M., Ford, P., Ito, K., & Barnes, P. J. (2006) · Respiratory Research · doi:10.1186/1465-9921-7-21 · Cited by 158
Queirós, A. C., Villamor, N., Clot, G., Martínez‐Trillos, A., Kulis, M., Navarro, A., Penas, E. M. M., Jayne, S., Majid, A., Richter, J., et al. (2014) · Leukemia · doi:10.1038/leu.2014.252 · Cited by 158
Ramos-Rodríguez, M., Raurell‐Vila, H., Colli, M. L., Alvelos, M. I., Subirana-Granés, M., Juan‐Mateu, J., Norris, R., Turatsinze, J., Nakayasu, E. S., Webb‐Robertson, B., et al. (2019) · Nature Genetics · doi:10.1038/s41588-019-0524-6 · Cited by 158
HLA-G gene repression is reversed by demethylation
Moreau, P., Mouillot, G., Rousseau, P., Marcou, C., Dausset, J. B., & Carosella, E. D. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0337539100 · Cited by 158
Multifactorial Etiology of Gastric Cancer
Zabaleta, J. (2012) · Methods in molecular biology · doi:10.1007/978-1-61779-612-8_26 · Cited by 157
Wu, H., Wu, X., Shen, L., & Zhang, Y. (2014) · Nature Biotechnology · doi:10.1038/nbt.3073 · Cited by 157
Birthweight, Maternal Weight Trajectories and Global DNA Methylation of LINE-1 Repetitive Elements
Michels, K. B., Harris, H. R., & Barault, L. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025254 · Cited by 157
Ghoshal, K., Datta, J., Majumder, S., Bai, S., Dong, X. C., Parthun, M. R., & Jacob, S. T. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.23.8302-8319.2002 · Cited by 157
Hackett, J. A., Reddington, J. P., Nestor, C. E., Dunican, D. S., Branco, M. R., Reichmann, J., Reik, W., Surani, M. A., Adams, I. R., & Meehan, R. R. (2012) · Development · doi:10.1242/dev.081661 · Cited by 157
Lam, P., Cheung, F., Tan, H., Wang, N., Yuen, M., & Feng, Y. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17040465 · Cited by 156
Goel, A., Mathupala, S. P., & Pedersen, P. L. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m300608200 · Cited by 155
Epigenetic regulation of the honey bee transcriptome: unravelling the nature of methylated genes
Forêt, S., Kucharski, R., Pittelkow, Y., Lockett, G. A., & Maleszka, R. (2009) · BMC Genomics · doi:10.1186/1471-2164-10-472 · Cited by 155
Genome-wide loss of 5-hmC is a novel epigenetic feature of Huntington's disease
Wang, F., Yang, Y., Lin, X., Wang, J.-Q., Yong-sheng, W., Xie, W., Wang, D., Zhu, S., Liao, Y.-Q., Sun, Q., et al. (2013) · Human Molecular Genetics · doi:10.1093/hmg/ddt214 · Cited by 155
Epigenetic regulation mechanisms of microRNA expression
Morales, S., Monzó, M., & Navarro, A. (2017) · BioMolecular Concepts · doi:10.1515/bmc-2017-0024 · Cited by 159
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Zhou, F., Balaraman, Y., Teng, M., Liu, Y., Singh, R. P., & Nephew, K. P. (2011) · Alcoholism Clinical and Experimental Research · doi:10.1111/j.1530-0277.2010.01391.x · Cited by 154
Prediction of genome-wide DNA methylation in repetitive elements
Zheng, Y., Joyce, B. T., Liu, L., Zhang, Z., Kibbe, W. A., Zhang, W., & Hou, L. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx587 · Cited by 154
Reid, G., Métivier, R., Lin, C., Denger, S., Ibberson, D., Ivacevic, T., Brand, H., Beneš, V., Liu, E. T., & Gannon, F. (2005) · Oncogene · doi:10.1038/sj.onc.1208662 · Cited by 154
Interplay Between Different Epigenetic Modifications and Mechanisms
Murr, R. (2010) · Advances in genetics · doi:10.1016/b978-0-12-380866-0.60005-8 · Cited by 154
Detection and Quantification of Methylation in DNA using Solid-State Nanopores
Shim, J., Humphreys, G. I., Venkatesan, B. M., Munz, J. M. A., Zou, X., Sathe, C., Schulten, K. J., Kosari, F., Nardulli, A. M., Vasmatzis, G., et al. (2013) · Scientific Reports · doi:10.1038/srep01389 · Cited by 153
Matsumoto, Y., Buemio, A., Chu, R. A., Vafaee, M., & Crews, D. P. (2013) · PLoS ONE · doi:10.1371/journal.pone.0063599 · Cited by 153
The epigenetic mechanism of mechanically induced osteogenic differentiation
Arnsdorf, E. J., Tummala, P., Castillo, A. B., Zhang, F., & Jacobs, C. R. (2010) · Journal of Biomechanics · doi:10.1016/j.jbiomech.2010.07.033 · Cited by 153
Development of histone deacetylase inhibitors for cancer treatment
Marchion, D. C., & Münster, P. N. (2007) · Expert Review of Anticancer Therapy · doi:10.1586/14737140.7.4.583 · Cited by 153
DNA methylation and chromatin structure: The puzzling CpG islands
Caiafa, P., & Zampieri, M. (2004) · Journal of Cellular Biochemistry · doi:10.1002/jcb.20325 · Cited by 153
Hashimoto, K., Otero, M., Imagawa, K., de Andrés, M. C., Coico, J. M., Roach, H. I., Oreffo, R. O. C., Marcu, K. B., & Goldring, M. B. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.421156 · Cited by 152
Transcriptional control of the glucocorticoid receptor: CpG islands, epigenetics and more
Turner, J. D., Alt, S. R., Cao, L., Vernocchi, S., Trifonova, S. T., Battello, N., & Muller, C. P. (2010) · Biochemical Pharmacology · doi:10.1016/j.bcp.2010.06.037 · Cited by 152
Houde, A.-A., Légaré, C., Biron, S., Lescelleur, O., Biertho, L. D., Marceau, S., Tchernof, A., Vohl, M., Hivert, M., & Bouchard, L. (2015) · BMC Medical Genetics · doi:10.1186/s12881-015-0174-1 · Cited by 152
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Harris, K. M., & McDade, T. W. (2018) · RSF The Russell Sage Foundation Journal of the Social Sciences · doi:10.7758/rsf.2018.4.4.01 · Cited by 152
Li, Y., Zheng, H., Wang, Q., Zhou, C., Wei, L., Liu, X., Zhang, W., Zhang, Y., Du, Z., Wang, X., et al. (2018) · Genome biology · doi:10.1186/s13059-018-1390-8 · Cited by 152
Miyamoto, K., Asada, K., Fukutomi, T., Okochi, E., Yagi, Y., Hasegawa, T., Asahara, T., Sügimura, T., & Ushijima, T. (2003) · Oncogene · doi:10.1038/sj.onc.1206146 · Cited by 152
Li, F., Papworth, M. A., Minczuk, M. A., Rohde, C., Zhang, Y., Ragozin, S., & Jeltsch, A. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl1035 · Cited by 152
Mechanical Regulation of Nuclear Structure and Function
Martins, R. P., Finan, J. D., Guilak, F., & Lee, D. A. (2012) · Annual Review of Biomedical Engineering · doi:10.1146/annurev-bioeng-071910-124638 · Cited by 151
Tissue- and Expression Level–Specific Chromatin Looping at Maizeb1Epialleles
Louwers, M., Bader, R., Haring, M., DRIEL, R. V., de Laat, W. L., & Stam, M. E. (2009) · The Plant Cell · doi:10.1105/tpc.108.064329 · Cited by 151
DNA methylation‐mediated epigenetic control
Rottach, A., Leonhardt, H., & Spada, F. (2009) · Journal of Cellular Biochemistry · doi:10.1002/jcb.22253 · Cited by 150
Epigenomics: Genome-Wide Study of Methylation Phenomena
(2002) · Current Issues in Molecular Biology · doi:10.21775/cimb.004.111 · Cited by 150
The Nonspecific Lethal Complex Is a Transcriptional Regulator in Drosophila
Raja, S. J., Charapitsa, I., Conrad, T., Vaquerizas, J. M., Gebhardt, P., Holz, H., Kadlec, J., Fraterman, S., Luscombe, N. M., & Akhtar, A. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.05.021 · Cited by 149
Two means of transcriptional reactivation within heterochromatin
Probst, A. V., Fransz, P. F., Paszkowski, J., & Scheid, O. M. (2003) · The Plant Journal · doi:10.1046/j.1365-313x.2003.01667.x · Cited by 149
Cortese, R., Lu, L., Yu, Y., Ruden, D., & Claud, E. C. (2016) · Epigenetics · doi:10.1080/15592294.2016.1155011 · Cited by 148
Dannenberg, L. O., & Edenberg, H. J. (2006) · BMC Genomics · doi:10.1186/1471-2164-7-181 · Cited by 148
Vogt, G. (2015) · Journal of Biosciences · doi:10.1007/s12038-015-9506-8 · Cited by 148
Forensic DNA methylation profiling—Potential opportunities and challenges
Vidaki, A., Daniel, B. E., & Court, D. S. (2013) · Forensic Science International Genetics · doi:10.1016/j.fsigen.2013.05.004 · Cited by 148
Gravina, G. L., Festuccia, C., Marampon, F., Popov, V. M., Pestell, R. G., ZANI, B. M., & Tombolini, V. (2010) · Molecular Cancer · doi:10.1186/1476-4598-9-305 · Cited by 148
An evaluation of methods correcting for cell-type heterogeneity in DNA methylation studies
McGregor, K., Bernatsky, S., Colmegna, I., Hudson, M., Pastinen, T., Labbe, A., & Greenwood, C. M. T. (2016) · Genome biology · doi:10.1186/s13059-016-0935-y · Cited by 148
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Mascolo, M., Siano, M., Ilardi, G., Russo, D., Merolla, F., Rosa, G. D., & Staibano, S. (2012) · International Journal of Molecular Sciences · doi:10.3390/ijms13022331 · Cited by 148
Lsh, an epigenetic guardian of repetitive elements
Huang, J. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh821 · Cited by 148
Rosmarin, A. G., Yang, Z., & Resendes, K. K. (2005) · Experimental Hematology · doi:10.1016/j.exphem.2004.08.015 · Cited by 121
Noer, A., Sørensen, A. L., Boquest, A. C., & Collas, P. (2006) · Molecular Biology of the Cell · doi:10.1091/mbc.e06-04-0322 · Cited by 147
DNA methylation profiles of CpG islands for cellular differentiation and development in mammals
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Ghosh, R. P., Horowitz-Scherer, R. A., Tv, N., Shlyakhtenko, L. S., & Woodcock, C. L. F. (2010) · Molecular and Cellular Biology · doi:10.1128/mcb.00379-10 · Cited by 150
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Makar, K. W., Pérez‐Melgosa, M., Shnyreva, M., Weaver, W. M., Fitzpatrick, D. R., & Wilson, C. B. (2003) · Nature Immunology · doi:10.1038/ni1004 · Cited by 147
Hughes, J. R., Cheng, J., Ventress, N., Prabhakar, S., Clark, K., Anguita, E., Gobbi, M. D., de Jong, P., Rubin, E., & Higgs, D. R. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0503401102 · Cited by 147
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Feng, F., Wang, H., Han, L., & Wang, S. (2008) · Journal of the American Chemical Society · doi:10.1021/ja8011963 · Cited by 146
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Derks, S., Lentjes, M. H. F. M., Hellebrekers, D. M. E. I., de Bruı̈ne, A. P., Herman, J. G., & van Engeland, M. (2004) · Analytical Cellular Pathology · doi:10.1155/2004/370301 · Cited by 146
Gene silencing by DNA methylation in haematological malignancies
Boultwood, J., & Wainscoat, J. S. (2007) · British Journal of Haematology · doi:10.1111/j.1365-2141.2007.06604.x · Cited by 146
Spotswood, H. T., & Turner, B. M. (2002) · Journal of Clinical Investigation · doi:10.1172/jci16547 · Cited by 146
Epigenetic regulation: a new research area for melatonin?
Korkmaz, A., & Reiter, R. J. (2007) · Journal of Pineal Research · doi:10.1111/j.1600-079x.2007.00509.x · Cited by 146
Heterochromatin?many flavours, common themes
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Siedlecki, P. S., Boy, R. G., Musch, T., Brueckner, B., Suhai, S., Lyko, F., & Zielenkiewicz, P. (2005) · Journal of Medicinal Chemistry · doi:10.1021/jm050844z · Cited by 146
Watanabe, Y., & Maekawa, M. (2010) · Advances in clinical chemistry · doi:10.1016/s0065-2423(10)52006-7 · Cited by 145
Novikova, S. I., He, F., Bai, J., Cutrufello, N. J., Lidow, M. S., & Undieh, A. S. (2008) · PLoS ONE · doi:10.1371/journal.pone.0001919 · Cited by 145
Rondelet, G., Maso, T. D., Willems, L., & Wouters, J. (2016) · Journal of Structural Biology · doi:10.1016/j.jsb.2016.03.013 · Cited by 145
DNA methylation aberrancies as a guide for surveillance and treatment of human cancers
Liang, G., & Weisenberger, D. J. (2017) · Epigenetics · doi:10.1080/15592294.2017.1311434 · Cited by 145
Means, mechanisms and consequences of adenine methylation in DNA
Boulias, K., & Greer, E. L. (2022) · Nature Reviews Genetics · doi:10.1038/s41576-022-00456-x · Cited by 145
Holz-Schietinger, C., Matje, D. M., & Reich, N. O. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.366625 · Cited by 145
Transcriptional Repression and Heterochromatin Formation by MBD1 and MCAF/AM Family Proteins
Ichimura, T., Watanabe, S., Sakamoto, Y., Aoto, T., Fujita, N., & Nakao, M. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m413654200 · Cited by 145
Velasco, G., Hubé, F., Rollin, J., Neuillet, D., Philippe, C., Bouzinba-Ségard, H., Galvani, A., Viégas-Pèquignot, E., & Francastel, C. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1000473107 · Cited by 144
Quantitative reconstruction of leukocyte subsets using DNA methylation
Accomando, W. P., Wiencke, J. K., Houseman, E. A., Nelson, H. H., & Kelsey, K. T. (2014) · Genome biology · doi:10.1186/gb-2014-15-3-r50 · Cited by 144
Adaptation to environmental stress at different timescales
Kristensen, T. N., Ketola, T., & Kronholm, I. (2018) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13974 · Cited by 144
PCNA Modifications for Regulation of Post-Replication Repair Pathways
Lee, K., & Myung, K. (2008) · Molecules and Cells · doi:10.1016/s1016-8478(23)13956-2 · Cited by 144
Genomic mechanisms and measurement of structural and numerical instability in cancer cells
Bayani, J., Selvarajah, S., Maire, G., Vukovic, B., Al-Romaih, K. I., Zieleńska, M., & Squire, J. A. (2006) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2006.10.006 · Cited by 144
Geiman, T. M., Sankpal, U. T., Robertson, A. K., Zhao, Y., Zhao, Y., & Robertson, K. D. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.04.058 · Cited by 144
Stancheva, I., Collins, A. L., den Veyver, I. B. V., Zoghbi, H. Y., & Meehan, R. R. (2016) · Molecular Cell · doi:10.1016/j.molcel.2016.06.007 · Cited by 144
Differential methylation of genes and repeats in land plantsPreprint
Rabinowicz, P. D., Citek, R. W., Budiman, M. A., Nunberg, A. N., Bedell, J. A., Lakey, N. D., O'Shaughnessy, A. L., Nascimento, L. U., McCombie, W. R., & Martienssen, R. A. (2005) · Genome Research · doi:10.1101/gr.4100405 · Cited by 144
Human ribosomal RNA gene arrays display a broad range of palindromic structures
Caburet, S., Conti, C., Schurra, C., Lebofsky, R., Edelstein, S. J., & Bensimon, A. (2005) · Genome Research · doi:10.1101/gr.3970105 · Cited by 143
Yohn, N. L., Bartolomei, M. S., & Blendy, J. A. (2015) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2015.03.002 · Cited by 143
Deng, H., Guo, Y., Song, H., Xiao, B., Sun, W., Liu, Z., Yu, X., Xia, T., Cui, L., & Guo, J. (2013) · Gene · doi:10.1016/j.gene.2012.12.103 · Cited by 143
Metadata
- Authors
- Bird, A.
- Affiliations
- Wellcome Centre for Cell Biology (GB)
- Corresponding author
- Bird, Adrian
- ORCID
- Bird, Adrian
- Venue
- Genes & Development
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2002-01-01
- Volume
- 16
- Issue
- 1
- Pages
- 6-21
- ISSN
- 0890-9369 (ISSN-L)
- 1549-5477
- OpenAlex
- W2121417064
- Cited by
- 7,124
- References
- 208
- Citations by year
- 2026: 178 · 2025: 199 · 2024: 247 · 2023: 222 · 2022: 284 · 2021: 327 · 2020: 318 · 2019: 328 · 2018: 327 · 2017: 426 · 2016: 408 · 2015: 416 · 2014: 415 · 2013: 409 · 2012: 382
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Genes & Development (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Wellcome Trust
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Syndromes and Imprinting
- Keywords
- epigenetic memory, genomic imprinting, Polycomb group proteins, Trithorax group proteins, transcriptional repression, epigenetic reprogramming, mammalian development, gene silencing, histone modifications, somatic cell nuclear transfer, epigenetic inheritance
- MeSH terms
- Animals, Embryonic and Fetal Development, Humans, Transcription, Genetic, Gene Expression Regulation, Developmental, DNA Methylation, Gene Silencing
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