The DOI matches its Crossref record; 206 of the 208 references it cites were found in a registry or an index.
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).
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“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
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
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
Flagged first, then by citations
2 of the 208 references couldn’t be matched to a known paper.
Research works printed but not linked: 3
- 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 401–500 of 1,038
The Human Dnmt2 Has Residual DNA-(Cytosine-C5) Methyltransferase Activity
Hermann, A., Schmitt, S., & Jeltsch, A. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m305448200 · Cited by 255
Reconfiguration of DNA methylation in aging
Zampieri, M., Ciccarone, F., Calabrese, R., Franceschi, C., Bürkle, A., & Caiafa, P. (2015) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2015.02.002 · Cited by 254
“Methylated cytosine, known as 5-methylcytosine (5mC), is considered the fifth base of DNA due to its non-random distribution in genome which introduces an epigenetic code (Bird, 2002; Jones and Takai, 2001; Suzuki and Bird, 2008; Takai and Jones, 2002).”
BackgroundKismeth: Analyzer of plant methylation states through bisulfite sequencing
Gruntman, E., Qi, Y., Slotkin, R. K., Roeder, T., Martienssen, R. A., & Sachidanandam, R. (2008) · BMC Bioinformatics · doi:10.1186/1471-2105-9-371 · Cited by 254
Lee, J. H., Khor, T. O., Shu, L., Su, Z., Fuentes, F., & Kong, A. T. (2012) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2012.09.008 · Cited by 254
NMDA hypofunction as a convergence point for progression and symptoms of schizophrenia
Snyder, M. A., & Gao, W. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00031 · Cited by 254
Akiyama, Y., Watkins, N., Suzuki, H., Jair, K.-W., van Engeland, M., Esteller, M., Sakai, H., Ren, C.-Y., Yuasa, Y., Herman, J. G., et al. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.23.8429-8439.2003 · Cited by 253
A Dnmt2-like protein mediates DNA methylation inDrosophila
Kunert, N., Marhold, J., Stanke, J., Stach, D., & Lyko, F. (2003) · Development · doi:10.1242/dev.00716 · Cited by 253
Weber, A. R., Krawczyk, C., Robertson, A. B., Kuśnierczyk, A., Vågbø, C. B., Schuermann, D., Klungland, A., & Schär, P. (2016) · Nature Communications · doi:10.1038/ncomms10806 · Cited by 252
Rational Therapeutic Combinations with Histone Deacetylase Inhibitors for the Treatment of Cancer
Thurn, K. T., Thomas, S., Moore, A. P., & Münster, P. N. (2011) · Future Oncology · doi:10.2217/fon.11.2 · Cited by 251
Fan, M., Yan, P. S., Hartman-Frey, C., Chen, L., Paik, H. H.-I., Oyer, S. L., Salisbury, J. D., Cheng, A. S. L., Li, L., Abbosh, P. H., et al. (2006) · Cancer Research · doi:10.1158/0008-5472.can-06-1666 · Cited by 251
The thrifty epigenotype: An acquired and heritable predisposition for obesity and diabetes?
Stöger, R. J. (2008) · BioEssays · doi:10.1002/bies.20700 · Cited by 251
Molecular Biology of Lung Cancer: Clinical Implications
Larsen, J. E., & Minna, J. D. (2011) · Clinics in Chest Medicine · doi:10.1016/j.ccm.2011.08.003 · Cited by 251
Dimethyl Sulfoxide Has an Impact on Epigenetic Profile in Mouse Embryoid Body
Iwatani, M., Ikegami, K., Kremenska, Y., Hattori, N., Tanaka, S., Yagi, S., & Shiota, K. (2006) · Stem Cells · doi:10.1634/stemcells.2005-0427 · Cited by 250
Functional Analysis of Promoter CPG-Methylation using a CpG-Free Luciferase Reporter Vector
Klug, M., & Rehli, M. (2006) · Epigenetics · doi:10.4161/epi.1.3.3327 · Cited by 250
The methylated component of the Neurospora crassa genome
Selker, E. U., Tountas, N. A., Cross, S. H., Margolin, B. S., Murphy, J. G., Bird, A. P., & Freitag, M. (2003) · Nature · doi:10.1038/nature01564 · Cited by 250
Self-citationDistinct regulation of histone H3 methylation at lysines 27 and 9 by CpG methylation in Arabidopsis
Mathieu, O., Probst, A. V., & Paszkowski, J. (2005) · The EMBO Journal · doi:10.1038/sj.emboj.7600743 · Cited by 250
Epigenetics and environment: a complex relationship
Aguilera, O., Fernández, A. F., Múñoz, A., & Fraga, M. F. (2010) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00068.2010 · Cited by 249
Grath, S., & Parsch, J. (2016) · Annual Review of Genetics · doi:10.1146/annurev-genet-120215-035429 · Cited by 249
Bouchard, L., RABASA-LHORET, R. P. R., Faraj, M., Lavoie, M.-È., Mill, J. S., Përusse, L., & Vohl, M. (2009) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.2009.28085 · Cited by 248
Schermelleh, L., Haemmer, A., Spada, F., Rösing, N., Meilinger, D., Rothbauer, U., Cardoso, M. C., & Leonhardt, H. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm432 · Cited by 247
Histones: At the Crossroads of Peptide and Protein Chemistry
Müller, M. M., & Muir, T. W. (2015) · Chemical Reviews · doi:10.1021/cr5003529 · Cited by 247
Oncogenic roles of DNA hypomethylation through the activation of cancer-germline genes
Tongelen, A. V., Loriot, A. E., & Smet, C. D. (2017) · Cancer Letters · doi:10.1016/j.canlet.2017.03.029 · Cited by 247
REST, a master transcriptional regulator in neurodegenerative disease
Hwang, J.-Y., & Zukin, R. S. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.12.008 · Cited by 247
Roth, T. L., & David Sweatt, J. (2011) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2010.02282.x · Cited by 246
Li, J., Pu, M., Hirasawa, R., Li, B.-Z., Huang, Y.-N., Zeng, R., Jing, N.-H., Chen, T., Li, E., Sasaki, H., et al. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.01380-07 · Cited by 246
Regional copy number–independent deregulation of transcription in cancer
Stransky, N., Vallot, C., Reyal, F., Bernard‐Pierrot, I., de Medina, S. G. D., Segraves, R., Rycke, Y. D., Elvin, P., Cassidy, A., Spraggon, C., et al. (2006) · Nature Genetics · doi:10.1038/ng1923 · Cited by 246
Machine learning and clinical epigenetics: a review of challenges for diagnosis and classification
Rauschert, S., Raubenheimer, K., Melton, P. E., & Huang, R. (2020) · Clinical Epigenetics · doi:10.1186/s13148-020-00842-4 · Cited by 248
Berghe, W. V. (2012) · Pharmacological Research · doi:10.1016/j.phrs.2012.03.007 · Cited by 245
Leptin Gene Epigenetic Adaptation to Impaired Glucose Metabolism During Pregnancy
Bouchard, L., Thibault, S., Guay, S., Santuré, M., Monpetit, A., St‐Pierre, J., Perron, P., & Brisson, D. (2010) · Diabetes Care · doi:10.2337/dc10-1024 · Cited by 245
Fujiki, K., Kano, F., Shiota, K., & Murata, M. (2009) · BMC Biology · doi:10.1186/1741-7007-7-38 · Cited by 244
González-Alzaga, B., Lacasaña, M., Aguilar-Garduño, C., Rodríguez‐Barranco, M., Ballester, F., Rebagliato, M., & Hernández, A. F. (2013) · Toxicology Letters · doi:10.1016/j.toxlet.2013.11.019 · Cited by 244
Kohl, P. K., Crampin, E. J., Quinn, T. A., & Noble, D. (2010) · Clinical Pharmacology & Therapeutics · doi:10.1038/clpt.2010.92 · Cited by 242
Transcription Factors Drive Tet2-Mediated Enhancer Demethylation to Reprogram Cell Fate
Sardina, J. L., Collombet, S., Tian, T. V., Gómez, A., Stefano, B. D., Berenguer, C., Brumbaugh, J., Stadhouders, R., Segura-Morales, C., Gut, M., et al. (2018) · Cell stem cell · doi:10.1016/j.stem.2018.08.016 · Cited by 242
Nutritional programming of disease: unravelling the mechanism
Langley‐Evans, S. C. (2008) · Journal of Anatomy · doi:10.1111/j.1469-7580.2008.00977.x · Cited by 241
Albuquerque, D., Stice, E. M., Rodríguez‐López, R., Manco, L., & Nóbrega, C. (2015) · Molecular Genetics and Genomics · doi:10.1007/s00438-015-1015-9 · Cited by 240
Mecp2 deficiency leads to delayed maturation and altered gene expression in hippocampal neurons
Smrt, R. D., Eaves-Egenes, J., Barkho, B. Z., Santistevan, N. J., Zhao, C., Aimone, J. B., Gage, F. H., & Zhao, X. (2007) · Neurobiology of Disease · doi:10.1016/j.nbd.2007.04.005 · Cited by 239
Kinde, B., Gabel, H. W., Gilbert, C. S., Griffith, E. C., & Greenberg, M. E. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1411269112 · Cited by 236
DNA methylation disruption reshapes the hematopoietic differentiation landscape
Izzo, F., Lee, S. C., Poran, A., Chaligne, R., Gaiti, F., Gross, B., Murali, R. R., Deochand, S. D., Ang, C., Jones, P. W., et al. (2020) · Nature Genetics · doi:10.1038/s41588-020-0595-4 · Cited by 236
Lee, H.-S. (2015) · Nutrients · doi:10.3390/nu7115467 · Cited by 236
Active DNA demethylation at enhancers during the vertebrate phylotypic period
Bogdanović, O., Smits, A. H., de la Calle‐Mustienes, E., Tena, J. J., Ford, E., Williams, R. M., Senanayake, U., Schultz, M. D., Hontelez, S., van Kruijsbergen, I., et al. (2016) · Nature Genetics · doi:10.1038/ng.3522 · Cited by 236
Emerging roles of TET proteins and 5-hydroxymethylcytosines in active DNA demethylation and beyond
Guo, J. U., Su, Y., Zhong, C., Ming, G.-L., & Song, H. (2011) · Cell Cycle · doi:10.4161/cc.10.16.17093 · Cited by 235
Control ofArabidopsisflowering: the chill before the bloom
Henderson, I. R., & Dean, C. (2004) · Development · doi:10.1242/dev.01294 · Cited by 234
Methylenetetrahydrofolate (MTHFR), the One-Carbon Cycle, and Cardiovascular Risks
Raghubeer, S., & Matsha, T. E. (2021) · Nutrients · doi:10.3390/nu13124562 · Cited by 233
DNA methylation-based predictors of health: applications and statistical considerations
Yousefi, P., Suderman, M. J., Langdon, R., Whitehurst, O., Smith, G. D., & Relton, C. L. (2022) · Nature Reviews Genetics · doi:10.1038/s41576-022-00465-w · Cited by 233
Embryonic stem cell and induced pluripotent stem cell: an epigenetic perspective
Liang, G., & Zhang, Y. (2012) · Cell Research · doi:10.1038/cr.2012.175 · Cited by 232
Epigenetics of cervical cancer. An overview and therapeutic perspectives
Dueñas‐González, A., Lizano, M., Candelaria, M., Cetina, L., Arce, C., & Cervera, E. (2005) · Molecular Cancer · doi:10.1186/1476-4598-4-38 · Cited by 232
Accuracy of DNA methylation pattern preservation by the Dnmt1 methyltransferase
Goyal, R. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl002 · Cited by 231
Evolution of decitabine development
Jabbour, E. J., Issa, J. J., Garcia‐Manero, G., & Kantarjian, H. M. (2008) · Cancer · doi:10.1002/cncr.23463 · Cited by 231
Wilson, A. G. (2008) · Journal of Periodontology · doi:10.1902/jop.2008.080172 · Cited by 231
Epigenetic Regulation of Tumor Necrosis Factor Alpha
Sullivan, K. E., Reddy, A. B. M., Dietzmann, K., Suriano, A. R., Kocieda, V., Stewart, M., & Bhatia, M. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.02429-06 · Cited by 231
SIRT1 Deacetylates the DNA Methyltransferase 1 (DNMT1) Protein and Alters Its Activities
Peng, L., Yuan, Z., Ling, H., Fukasawa, K., Robertson, K. D., Olashaw, N., Koomen, J. M., Chen, J., Lane, W. S., & Seto, E. (2011) · Molecular and Cellular Biology · doi:10.1128/mcb.06147-11 · Cited by 230
Intragenic DNA methylation in transcriptional regulation, normal differentiation and cancer
Kulis, M., Queirós, A. C., Beekman, R., & Martín-Subero, J. I. (2013) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2013.08.001 · Cited by 230
The fundamental role of epigenetics in hematopoietic malignancies
Galm, O., Herman, J. G., & Baylin, S. B. (2005) · Blood Reviews · doi:10.1016/j.blre.2005.01.006 · Cited by 230
DNA methylation methods: Global DNA methylation and methylomic analyses
Li, S., & Tollefsbol, T. O. (2020) · Methods · doi:10.1016/j.ymeth.2020.10.002 · Cited by 230
Bridging the transgenerational gap with epigenetic memory
Lim, J. P., & Brunet, A. (2013) · Trends in Genetics · doi:10.1016/j.tig.2012.12.008 · Cited by 228
Beaujean, N., Taylor, J., Gardner, J., Wilmut, I., Meehan, R. R., & Young, L. E. (2004) · Biology of Reproduction · doi:10.1095/biolreprod.103.026559 · Cited by 228
Dynamics of dna methylation and its functions in plant growth and development
Kumar, S., & Mohapatra, T. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2021.596236 · Cited by 227
Phalke, S., Nickel, O., Walluscheck, D., Hortig, F., Onorati, M. C., & Reuter, G. (2009) · Nature Genetics · doi:10.1038/ng.360 · Cited by 226
Epigenetic reprogramming of cancer cells via targeted DNA methylation
Rivenbark, A. G., Stolzenburg, S., Beltrán, A. S., Yuan, X., Rots, M. G., Strahl, B. D., & Blancafort, P. (2012) · Epigenetics · doi:10.4161/epi.19507 · Cited by 226
Epigenetic Cross-Talk between DNA Methylation and Histone Modifications in Human Cancers
Kondo, Y. (2009) · Yonsei Medical Journal · doi:10.3349/ymj.2009.50.4.455 · Cited by 226
Rishi, V., Bhattacharya, P., Chatterjee, R., Rozenberg, J. M., Zhao, J., Glass, K., FitzGerald, P. C., & Vinson, C. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1008688107 · Cited by 225
Mediators of reprogramming: transcription factors and transitions through mitosis
Egli, D. M., Birkhoff, G., & Eggan, K. C. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2439 · Cited by 225
Kovacheva, V., Mellott, T. J., Davison, J. M., Wagner, N., G.‐Coviella, I. L., Schnitzler, A. C., & Blusztajn, J. K. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m705539200 · Cited by 225
Song, Y., Ji, D., Li, S., Wang, P., Li, Q., & Xiang, F. (2012) · PLoS ONE · doi:10.1371/journal.pone.0041274 · Cited by 225
Predictors of global methylation levels in blood DNA of healthy subjects: a combined analysis
Zhu, Z.-Z., Hou, L., Bollati, V., Tarantini, L., Marinelli, B., Cantone, L., Yang, A. S., Vokonas, P., Lissowska, J., Fustinoni, S., et al. (2010) · International Journal of Epidemiology · doi:10.1093/ije/dyq154 · Cited by 226
Adaptation to Global Change: A Transposable Element–Epigenetics Perspective
Rey, O., Danchin, É., Mirouze, M., Loot, C., & Blanchet, S. (2016) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2016.03.013 · Cited by 225
DNA Methylation Regulates Cocaine-Induced Behavioral Sensitization in Mice
Anier, K., Malinovskaja, K., Aonurm‐Helm, A., Zharkovsky, A., & Kalda, A. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2010.128 · Cited by 224
Review article: Epigenetic control of fetal gene expression
Nafee, T. M., Farrell, W., Carroll, W. D., Fryer, A. A., & Ismail, K. (2007) · BJOG An International Journal of Obstetrics & Gynaecology · doi:10.1111/j.1471-0528.2007.01528.x · Cited by 224
Epigenome in Early Mammalian Development: Inheritance, Reprogramming and Establishment
Xu, Q., & Xie, W. (2017) · Trends in Cell Biology · doi:10.1016/j.tcb.2017.10.008 · Cited by 224
Allegrucci, C., Thurston, A., Lucas, E. S., & Young, L. E. (2005) · Reproduction · doi:10.1530/rep.1.00360 · Cited by 223
Hofmeister, C. C., Zhang, J., Knight, K. L., Le, P. T., & Stiff, P. J. (2006) · Bone Marrow Transplantation · doi:10.1038/sj.bmt.1705538 · Cited by 223
A cross-package Bioconductor workflow for analysing methylation array data
Maksimovic, J., Phipson, B., & Oshlack, A. (2016) · F1000Research · doi:10.12688/f1000research.8839.3 · Cited by 224
Omole, A. E., & Fakoya, A. O. J. (2018) · PeerJ · doi:10.7717/peerj.4370 · Cited by 223
Targeting CDK9 Reactivates Epigenetically Silenced Genes in Cancer
Zhang, H., Pandey, S., Travers, M. E., Sun, H., Morton, G. C., Madžo, J., Chung, W., Khowsathit, J., Pérez, Ó. C., Barrero, C. A., et al. (2018) · Cell · doi:10.1016/j.cell.2018.09.051 · Cited by 223
Epigenetic Changes in Early Life and Future Risk of Obesity
Lillycrop, K. A., & Burdge, G. C. (2011) · International Journal of Obesity · doi:10.1038/ijo.2010.122 · Cited by 222
Bock, C., Paulsen, M., Tierling, S., Mikeska, T., Lengauer, T., & Walter, J. (2006) · PLoS Genetics · doi:10.1371/journal.pgen.0020026 · Cited by 222
The Role of DNA Methylation in Cardiovascular Risk and Disease
Zhong, J., Agha, G., & Baccarelli, A. (2016) · Circulation Research · doi:10.1161/circresaha.115.305206 · Cited by 222
Gene silencing in mammalian cells and the spread of DNA methylation
Turker, M. S. (2002) · Oncogene · doi:10.1038/sj.onc.1205599 · Cited by 222
Epigenetics of glioblastoma multiforme: From molecular mechanisms to therapeutic approaches
Uddin, M. S., Mamun, A. A., Alghamdi, B. S. A., Tewari, D., Jeandet, P., Sarwar, M. S., & Ashraf, G. M. (2020) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2020.12.015 · Cited by 224
Epigenetic control in rheumatoid arthritis synovial fibroblasts
Karouzakis, E., Gay, R. E., Gay, S., & Neidhart, M. (2009) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2009.55 · Cited by 220
Epigenetic alterations regulate estradiol-induced enhancement of memory consolidation
Zhao, Z., Fan, L., & Frick, K. M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0910578107 · Cited by 220
De novo CpG Island Methylation in Human Cancer Cells
Jair, K.-W., Bachman, K. E., Suzuki, H., Ting, A. H., Rhee, I. P., Yen, R.-W. C., Baylin, S. B., & Schuebel, K. E. (2006) · Cancer Research · doi:10.1158/0008-5472.can-05-1980 · Cited by 219
Majid, S., Dar, A. A., Ahmad, A. E., Hirata, H., Kawakami, K., Shahryari, V., Saini, S., Tanaka, Y., Dahiya, A. V., Khatri, G., et al. (2009) · Carcinogenesis · doi:10.1093/carcin/bgp042 · Cited by 219
Dnmt3L is a transcriptional repressor that recruits histone deacetylase
Deplus, R. (2002) · Nucleic Acids Research · doi:10.1093/nar/gkf509 · Cited by 218
Generic eukaryotic core promoter prediction using structural features of DNAPreprint
Abeel, T., Saeys, Y., Bonnet, É., Rouzé, P., & de Peer, Y. V. (2007) · Genome Research · doi:10.1101/gr.6991408 · Cited by 218
Gendrel, A.-V., Apedaile, A., Coker, H. A., Termanis, A., Zvetkova, I., Godwin, J., Tang, A., Huntley, D. M., Montana, G., Taylor, S., et al. (2012) · Developmental Cell · doi:10.1016/j.devcel.2012.06.011 · Cited by 217
Putnam, H. M., Davidson, J. M., & Gates, R. D. (2016) · Evolutionary Applications · doi:10.1111/eva.12408 · Cited by 218
Dynamic epigenomic landscapes during early lineage specification in mouse embryos
Zhang, Y., Xiang, Y., Yin, Q., Du, Z., Xu, P., Wang, Q., Fidalgo, M., Xia, W., Li, Y., Zhao, Z., et al. (2017) · Nature Genetics · doi:10.1038/s41588-017-0003-x · Cited by 217
Allele‐specific histone lysine methylation marks regulatory regions at imprinted mouse genes
Fournier, C., Goto, Y., Ballestar, E., Delaval, K., Hever, A. M., Esteller, M., & Feil, R. (2002) · The EMBO Journal · doi:10.1093/emboj/cdf655 · Cited by 217
Hardy, T., Zeybel, M., Day, C. P., Dipper, C., Masson, S., McPherson, S., Henderson, E., Tiniakos, D., White, S., French, J., et al. (2017) · Gut · doi:10.1136/gutjnl-2016-311526 · Cited by 216
Abdolmaleky, H. M., Smith, C. L., Faraone, S. V., Shafa, R., Stone, W., Glatt, S. J., & Tsuang, M. T. (2004) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.20142 · Cited by 216
Epigenetic Regulation in Human Brain—Focus on Histone Lysine Methylation
Akbarian, S., & Huang, H. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.08.015 · Cited by 216
High-throughput bisulfite sequencing in mammalian genomes
Smith, Z. D., Gu, H., Bock, C., Gnirke, A., & Meissner, A. (2009) · Methods · doi:10.1016/j.ymeth.2009.05.003 · Cited by 216
Epialleles via DNA methylation: consequences for plant evolution
Kalisz, S., & Purugganan, M. D. (2004) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2004.03.034 · Cited by 216
Urea cycle dysregulation in non-alcoholic fatty liver disease
Chiara, F. D., Heebøll, S., Marrone, G., Montoliu, C., Hamilton-Dutoit, S. J., Ferrandez, A., Andreola, F., Rombouts, K., Grønbæk, H., Felipo, V., et al. (2018) · Journal of Hepatology · doi:10.1016/j.jhep.2018.06.023 · Cited by 216
Epigenetics in cancer therapy and nanomedicine
Roberti, A., Valdes, A. F., Torrecillas, R., Fraga, M. F., & Fernández, A. F. (2019) · Clinical Epigenetics · doi:10.1186/s13148-019-0675-4 · Cited by 216
Molecular analysis of PRC2 recruitment to DNA in chromatin and its inhibition by RNA
Wang, X., Paucek, R. D., Gooding, A. R., Brown, Z. Z., Ge, E. J., Muir, T. W., & Cech, T. R. (2017) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.3487 · Cited by 215
Wang, D., Szyf, M., Benkelfat, C., Provençal, N., Turecki, G., Caramaschi, D., Côté, S. M., Vitaro, F., Tremblay, R. E., & Booij, L. (2012) · PLoS ONE · doi:10.1371/journal.pone.0039501 · Cited by 214
Terranova, R., Agherbi, H., Boned, A., Méresse, S., & Djabali, M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0507425103 · Cited by 214
DNA methylation-based forensic tissue identification
Frumkin, D., Wasserstrom, A., Budowle, B., & Davidson, A. (2011) · Forensic Science International Genetics · doi:10.1016/j.fsigen.2010.12.001 · Cited by 214
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
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