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The Nuclear DNA Base 5-Hydroxymethylcytosine Is Present in Purkinje Neurons and the Brain
Open accessAbstract
Despite the importance of epigenetic regulation in neurological disorders, little is known about neuronal chromatin. Cerebellar Purkinje neurons have large and euchromatic nuclei, whereas granule cell nuclei are small and have a more typical heterochromatin distribution. While comparing the abundance of 5-methylcytosine in Purkinje and granule cell nuclei, we detected the presence of an unusual DNA nucleotide. Using thin-layer chromatography, high-pressure liquid chromatography, and mass spectrometry, we identified the nucleotide as 5-hydroxymethyl-2'-deoxycytidine (hmdC). hmdC constitutes 0.6% of total nucleotides in Purkinje cells, 0.2% in granule cells, and is not present in cancer cell lines. hmdC is a constituent of nuclear DNA that is highly abundant in the brain, suggesting a role in epigenetic control of neuronal function.
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“5-hydroxymethylcytosine, which is produced by the addition of hydroxyl groups to 5-methylcytosine under the action of the ten-eleven translocation (TET) enzymes (Fig. 2).59,60”
From Epigenetic regulation in major depression and other stress-related disorders: molecular mechanisms, clinical relevance and therapeutic potential (2023) · cites this paper as [60]
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“This enables FANS purification of target nuclei for assessment of DNA, nascent RNA transcription in the specific cell-type of interest, as well as proteomic analysis of histone modifications or transcription factor binding120,121.”
From Decoding neuroproteomics: integrating the genome, translatome and functional anatomy (2014) · cites this paper as [121]
In the citing paper
“First, neurons have high levels of hydroxymethylcytosine (hmC), a derivative of mC that may have distinct functional roles (Kriaucionis and Heintz, 2009; Mellén et al., 2017).”
From Single-Cell Sequencing of Brain Cell Transcriptomes and Epigenomes (2021) · cites this paper as Kriaucionis and Heintz, 2009
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Cites
A translational profiling approach for the molecular characterization of CNS cell types
Heiman, M., Schaefer, A., Gong, S., Peterson, J. D., Day, M., Ramsey, K. E., Suárez-Fariñas, M., Schwarz, C., Stephan, D. A., Surmeier, D. J., et al. (2008) · Cell · doi:10.1016/j.cell.2008.10.028 · Cited by 1,134
Self-citationApplication of a translational profiling approach for the comparative analysis of CNS cell types
Doyle, J. P., Dougherty, J. D., Heiman, M., Schmidt, E. F., Stevens, T. R., Ma, G., Bupp, S., Shrestha, P., Shah, R. D., Doughty, M. L., et al. (2008) · Cell · doi:10.1016/j.cell.2008.10.029 · Cited by 912
Self-citationValinluck, V. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh739 · Cited by 756
Wyatt, G. R., & Cohen, S. (1953) · Biochemical Journal · doi:10.1042/bj0550774 · Cited by 608
The Colorful History of Active DNA Demethylation
Ooi, S. K. T., & Bestor, T. H. (2008) · Cell · doi:10.1016/j.cell.2008.06.009 · Cited by 537
The presence of 5-hydroxymethylcytosine in animal deoxyribonucleic acid
Penn, N. W., SUWALSKI, R. T., O'Riley, C., Bojanowski, K., & Yura, R. (1972) · Biochemical Journal · doi:10.1042/bj1260781 · Cited by 280
Gommers-Ampt, J., & Borst, P. (1995) · The FASEB Journal · doi:10.1096/fasebj.9.11.7649402 · Cited by 126
Tardy-Planechaud, S. (1997) · Nucleic Acids Research · doi:10.1093/nar/25.3.553 · Cited by 88
Oxidative damage to 5-methylcytosine in DNA
Zuo, S., Boorstein, R. J., & Teebor, G. W. (1995) · Nucleic Acids Research · doi:10.1093/nar/23.16.3239 · Cited by 87
Reaction of bisulfite with the 5-hydroxymethyl group in pyrimidines and in phage DNAs
Hayatsu, H., & Shiragami, M. (1979) · Biochemistry · doi:10.1021/bi00571a013 · Cited by 85
Flagged first, then by citations
Research works printed but not linked: 1
- Ramsahoye B. H., Methods Mol. Biol. 200, 9 (2002).Medline
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Epigenetic mechanisms underlying nervous system diseases
Qureshi, I., & Mehler, M. F. (2018) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63233-3.00005-1 · Cited by 70
Methods for detection of cytosine and thymine modifications in DNA
Berney, M., & McGouran, J. F. (2018) · Nature Reviews Chemistry · doi:10.1038/s41570-018-0044-4 · Cited by 69
Suppression of TET1-Dependent DNA Demethylation Is Essential for KRAS-Mediated Transformation
Wu, B.-K., & Brenner, C. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.10.063 · Cited by 69
Epigenetics in Neurodevelopment: Emerging Role of Circular RNA
Meng, S., Zhou, H., Feng, Z., Xu, Z., Tang, Y., & Wu, M. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00327 · Cited by 71
“Brain DNA has one of the highest levels of m5Cs in human organs (Kriaucionis and Heintz, 2009; LaSalle et al., 2013), and DNA methylation is required for neuronal differentiation in mammals (Takizawa et al., 2001; Mohn et al., 2008).”
BackgroundNew themes in the biological functions of 5‐methylcytosine and 5‐hydroxymethylcytosine
Moen, E. L., Mariani, C. J., Zullow, H. J., Jeff‐Eke, M., Litwin, E., Nikitas, J. N., & Godley, L. A. (2014) · Immunological Reviews · doi:10.1111/imr.12242 · Cited by 66
Renčiuk, D., Blacque, O., Vorlı́čková, M., & Spingler, B. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt738 · Cited by 67
MBD2 and MBD3: elusive functions and mechanisms
Menafra, R., & Stunnenberg, H. G. (2014) · Frontiers in Genetics · doi:10.3389/fgene.2014.00428 · Cited by 67
Binding Analysis of Methyl-CpG Binding Domain of MeCP2 and Rett Syndrome Mutations
Yang, Y., Kucukkal, T. G., Li, J., Alexov, E., & Cao, W. (2016) · ACS Chemical Biology · doi:10.1021/acschembio.6b00450 · Cited by 67
Narne, P., Pandey, V., & Phanithi, P. B. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1141-6 · Cited by 71
“among the congeners of active DNA demethylation in the brain [88, 89].”
BackgroundSui, C., Wang, T., Zhou, Y., Yin, H., Meng, X., Zhang, S., Waterhouse, G. I. N., Xu, Q. H., Zhuge, Y., & Ai, S. (2018) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2018.11.054 · Cited by 68
Porcellini, E., Laprovitera, N., Riefolo, M., Ravaioli, M., Garajova, I., & Ferracin, M. (2018) · Cancer Letters · doi:10.1016/j.canlet.2018.01.049 · Cited by 66
N 6-Hydroxymethyladenine: a hydroxylation derivative of N6-methyladenine in genomic DNA of mammals
Xiong, J., Ye, T.-T., Ma, C.-J., Cheng, Q.-Y., Yuan, B., & Feng, Y. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky1218 · Cited by 67
DNA Modification Readers and Writers and Their Interplay
Rausch, C., Hastert, F. D., & Cardoso, M. C. (2019) · Journal of Molecular Biology · doi:10.1016/j.jmb.2019.12.018 · Cited by 67
Sen, A., Cingolani, P., Senut, M., Land, S. J., Mercado‐García, A., Téllez‐Rojo, M. M., Baccarelli, A., Wright, R. O., & Ruden, D. M. (2015) · Epigenetics · doi:10.1080/15592294.2015.1050172 · Cited by 69
Ten Eleven Translocation Enzymes and 5-Hydroxymethylation in Mammalian Development and Cancer
Kinney, S. R. M., & Pradhan, S. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-9967-2_3 · Cited by 68
DNA methylation dynamics in muscle development and disease
Carrió, E. (2015) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2015.00019 · Cited by 67
Causes and Consequences of Age-Related Changes in DNA Methylation: A Role for ROS?
Rang, F. J., & Boonstra, J. (2014) · Biology · doi:10.3390/biology3020403 · Cited by 65
Epigenetic control of adult skeletal muscle stem cell functions
Segalés, J., Perdiguero, E., & Muñoz‐Cánoves, P. (2014) · FEBS Journal · doi:10.1111/febs.13065 · Cited by 66
Insights into DNA hydroxymethylation in the honeybee from in-depth analyses of TET dioxygenase
Wojciechowski, M., Rafalski, D., Kucharski, R., Misztal, K., Maleszka, J., Bochtler, M., & Maleszka, R. (2014) · Open Biology · doi:10.1098/rsob.140110 · Cited by 73
Walker, D. L., Bhagwate, A. V., Baheti, S., Smalley, R. L., Hilker, C. A., Sun, Z., & Cunningham, J. M. (2015) · Epigenomics · doi:10.2217/epi.15.64 · Cited by 69
DNA-Methylation: Master or Slave of Neural Fate Decisions?
Stricker, S. H., & Götz, M. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00005 · Cited by 66
“The first of these 5mC oxidation products to be reported was 5hmC (C5-hydroxymethylcytosine) (Kriaucionis and Heintz, 2009; Tahiliani et al., 2009); 5fC (C5-formylcytosine), and 5caC (C5-carboxylcytosine) followed later.”
BackgroundBAC Transgenic Mice and the GENSAT Database of Engineered Mouse StrainsPreprint
Schmidt, E. F., Kus, L., Gong, S., & Heintz, N. (2013) · Cold Spring Harbor Protocols · doi:10.1101/pdb.top073692 · Cited by 65
Self-citationThe potential of DNA methylation as a biomarker for obesity and smoking
Heikkinen, A., Bollepalli, S., & Ollikainen, M. (2022) · Journal of Internal Medicine · doi:10.1111/joim.13496 · Cited by 70
Epigenetic changes in the developing brain: Effects on behavior
Keverne, E. B., Pfaff, D. W., & Tabansky, I. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1501482112 · Cited by 68
Mitochondria in health, aging and diseases: the epigenetic perspective
D’Aquila, P., Bellizzi, D., & Passarino, G. (2015) · Biogerontology · doi:10.1007/s10522-015-9562-3 · Cited by 66
DNA Methylation Dynamics in Neurogenesis
Wang, Z., Tang, B., He, Y., & Jin, P. (2016) · Epigenomics · doi:10.2217/epi.15.119 · Cited by 69
Lin, I., Chen, Y., & Hsu, M. (2017) · PLoS ONE · doi:10.1371/journal.pone.0170779 · Cited by 69
Neuroepigenetic mechanisms in disease
Christopher, M. A., Kyle, S. M., & Katz, D. J. (2017) · Epigenetics & Chromatin · doi:10.1186/s13072-017-0150-4 · Cited by 69
Decoding neuroproteomics: integrating the genome, translatome and functional anatomy
Kitchen, R. R., Rozowsky, J. S., Gerstein, M. B., & Nairn, A. C. (2014) · Nature Neuroscience · doi:10.1038/nn.3829 · Cited by 63
Ontogeny, distribution and potential roles of 5-hydroxymethylcytosine in human liver function
Ivanov, M., Kals, M., Kacevska, M., Barragán, I., Kasuga, K., Rane, A., Metspalu, A., Milani, L. A., & Ingelman‐Sundberg, M. (2013) · Genome biology · doi:10.1186/gb-2013-14-8-r83 · Cited by 65
Interindividual Variability in Stress Susceptibility: A Role for Epigenetic Mechanisms in PTSD
Zovkic, I. B., Meadows, J. P., Kaas, G. A., & Sweatt, J. D. (2013) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2013.00060 · Cited by 66
Epigenetics of Memory and Plasticity
Woldemichael, B. T., Bohacek, J., Gapp, K., & Mansuy, I. M. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-420170-5.00011-8 · Cited by 66
Cisternas, C. D., Cortes, L. R., Bruggeman, E. C., Yao, B., & Forger, N. G. (2019) · Epigenetics · doi:10.1080/15592294.2019.1649528 · Cited by 69
“5hmC is highly enriched in neurons [22], and the global level of 5hmC is approximately ten-fold higher in the central nervous system than in somatic tissues [23,24].”
BackgroundThe epigenomic interface between genome and environment in common complex diseases
Bell, C. G., & Beck, S. (2010) · Briefings in Functional Genomics · doi:10.1093/bfgp/elq026 · Cited by 64
Deciphering nucleic acid modifications by chemical derivatization-mass spectrometry analysis
Lan, M., Yuan, B., & Feng, Y. (2018) · Chinese Chemical Letters · doi:10.1016/j.cclet.2018.04.021 · Cited by 66
Udali, S., Guarini, P., Moruzzi, S., Ruzzenente, A., Tammen, S. A., Guglielmi, A., Conci, S., Pattini, P., Olivieri, O., Corrocher, R., et al. (2015) · Hepatology · doi:10.1002/hep.27823 · Cited by 64
Progress in mitochondrial epigenetics
Manev, H., & Dzitoyeva, S. (2013) · BioMolecular Concepts · doi:10.1515/bmc-2013-0005 · Cited by 64
Li, W., Gong, L., & Bayley, H. (2013) · Angewandte Chemie International Edition · doi:10.1002/anie.201300413 · Cited by 65
Diede, S. J., Guenthoer, J., Geng, L. N., Mahoney, S. E., Marotta, M. L., Olson, J. M., Tanaka, H., & Tapscott, S. J. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0907606106 · Cited by 64
The Dynamic Nature of DNA Methylation: A Role in Response to Social and Seasonal Variation
Alvarado, S. G., Fernald, R. D., Storey, K. B., & Szyf, M. (2014) · Integrative and Comparative Biology · doi:10.1093/icb/icu034 · Cited by 67
Weaver, I. C. G., Korgan, A. C., Lee, K., Wheeler, R. V., Hundert, A. S., & Goguen, D. (2017) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2017.00041 · Cited by 69
“…in compensatory upregulation of Tet2, Tet3 and other genes required for demethylation (e.g., Gadd45b, Smug1, Apobec1, Tdg; Jarome et al., 2015; Kumar et al., 2015), overexpression of TET1 protein (Kaas et al., 2013) and DNA methylation inhibition (Telese et al., 2015; Halder et al., 2016)…”
BackgroundEpigenetic regulation of intestinal stem cells by Tet1-mediated DNA hydroxymethylationPreprint
Kim, R., Sheaffer, K. L., Choi, I., Won, K., & Kaestner, K. H. (2016) · Genes & Development · doi:10.1101/gad.288035.116 · Cited by 62
“Recently, oxidation of 5mC to 5-hydroxymethylcytosine (5hmC) by the teneleven translocation (TET) gene family was proposed as a novel mechanism for removal of 5mC (Kriaucionis and Heintz 2009; Tahiliani et al. 2009).”
BackgroundChowdhury, B., Cho, I., Hahn, N. M., & Irudayaraj, J. (2014) · Analytica Chimica Acta · doi:10.1016/j.aca.2014.09.020 · Cited by 64
The role of epigenetic mechanisms and processes in autoimmune disorders
Greer, J. M., & McCombe, P. (2012) · Biologics · doi:10.2147/btt.s24067 · Cited by 68
Global hypomethylation and promoter methylation in small intestinal neuroendocrine tumors
Fotouhi, O., Fahmideh, M. A., Kjellman, M., Sulaiman, L. R., Höög, A., Zedenius, J., Hashemi, J., & Larsson, C. (2014) · Epigenetics · doi:10.4161/epi.28936 · Cited by 64
Pull-down of 5-hydroxymethylcytosine DNA using JBP1-coated magnetic beads
Robertson, A. B., Dahl, J. A., Ougland, R., & Klungland, A. (2012) · Nature Protocols · doi:10.1038/nprot.2011.443 · Cited by 63
Fneich, S., Dheilly, N. M., Adema, C. M., Rognon, A., Reichelt, M., Bulla, J., Grunau, C., & Cosseau, C. (2013) · Parasites & Vectors · doi:10.1186/1756-3305-6-167 · Cited by 67
Active DNA demethylation by oxidation and repair
Gong, Z., & Zhu, J. (2011) · Cell Research · doi:10.1038/cr.2011.140 · Cited by 62
Direct Decarboxylation of 5-Carboxylcytosine by DNA C5- Methyltransferases
Liutkevičiūtė, Z., Kriukienė, E., Ličytė, J., Narmontė, M., Urbanavičiūtė, G., & Klimašauskas, S. (2014) · Journal of the American Chemical Society · doi:10.1021/ja5019223 · Cited by 63
Epigenetics, microbiota, and intraocular inflammation: New paradigms of immune regulation in the eye
Wen, X., Hu, X., Li, M., Ge, X., Deng, Y., Bible, P. W., & Wei, L. (2018) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2018.01.001 · Cited by 65
“…of iron-dependent oxygenases, mediates a process that combines deamination and oxidation of 5-methyl-cytosine to form 5-hydroxymethyl-cytosine (Kriaucionis and Heintz, 2009; Tahiliani et al., 2009), 5-formylcytosine, and 5-carboxylcytosine (He et al., 2011; Ito et al., 2011), sequentially…”
Nutrient-driven O-GlcNAc cycling – think globally but act locally
Harwood, K. R., & Hanover, J. A. (2014) · Journal of Cell Science · doi:10.1242/jcs.113233 · Cited by 63
TET-Mediated Epigenetic Regulation in Immune Cell Development and Disease
Tsiouplis, N. J., Bailey, D. W., Chiou, L. F., Wissink, F. J., & Tsagaratou, A. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.623948 · Cited by 63
“It is most abundant in Purkinje neurons, where it comprises ∼40% of 5mC levels (Kriaucionis and Heintz, 2009).”
BackgroundKuehner, J. N., Chen, J., Bruggeman, E. C., Wang, F., Li, Y., Xu, C., McEachin, Z. T., Li, Z., Chen, L., Hales, C. M., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109042 · Cited by 60
“5hmC emerged as a key DNA modification in the nervous system due to its significant enrichment in the brain (Kriaucionis and Heintz, 2009) and its ability to regulate neuronal-Kuehner specific gene expression during neural progenitor cell differentiation (Li et al., 2017).”
Lyons, L. C., Vanrobaeys, Y. S., & Abel, T. G. (2023) · Journal of Neurochemistry · doi:10.1111/jnc.15787 · Cited by 69
“Hydroxymethylation has been associated with bidirectional gene regulation, with enhanced expression seen for some genes (Kriaucionis & Heintz, 2009; Li & Liu, 2011; Meng et al., 2015).”
BackgroundEpigenetic regulation of genomic imprinting from germ line to preimplantation
MacDonald, W. A., & Mann, M. R. W. (2013) · Molecular Reproduction and Development · doi:10.1002/mrd.22220 · Cited by 69
DNA methylation, the early-life social environment and behavioral disorders
Szyf, M. (2011) · Journal of Neurodevelopmental Disorders · doi:10.1007/s11689-011-9079-2 · Cited by 63
DNA unmethylome profiling by covalent capture of CpG sites
Kriukienė, E., Labrie, V., Khare, T., Urbanavičiūtė, G., Lapinaitė, A., Koncevičius, K., Li, D., Wang, T., Pai, S., Ptak, C., et al. (2013) · Nature Communications · doi:10.1038/ncomms3190 · Cited by 62
Epigenetic Mechanisms in Experience-Driven Memory Formation and Behavior
Puckett, R. E., & Lubin, F. D. (2011) · Epigenomics · doi:10.2217/epi.11.86 · Cited by 67
Anticancer Natural Compounds as Epigenetic Modulators of Gene Expression
Ratovitski, E. A. (2017) · Current Genomics · doi:10.2174/1389202917666160803165229 · Cited by 66
“In addition for being transcriptional repressor, the MBD2 protein exhibits demethylase activity in vitro [251-262].”
BackgroundHrit, J. A., Goodrich, L., Cheng, L., Wang, B.-A., Nie, J., Cui, X., Martin, E. A., Simental, E., Fernandez, J. A., Liu, M. Y., et al. (2018) · eLife · doi:10.7554/elife.34870 · Cited by 63
Hypoxia, Epithelial-Mesenchymal Transition, and TET-Mediated Epigenetic Changes
Kao, S.-H., Wu, K., & Lee, W. (2016) · Journal of Clinical Medicine · doi:10.3390/jcm5020024 · Cited by 64
5‐Formylcytosine Could Be a Semipermanent Base in Specific Genome Sites
Su, M., Kirchner, A., Stazzoni, S., Müller, M., Wagner, M., Schröder, A. S., & Carell, T. (2016) · Angewandte Chemie International Edition · doi:10.1002/anie.201605994 · Cited by 62
Third‐Generation Sequencing of Epigenetic DNA
Searle, B., Müller, M., Carell, T., & Kellett, A. (2022) · Angewandte Chemie International Edition · doi:10.1002/anie.202215704 · Cited by 64
An epigenetic hypothesis for the genomic memory of pain
Alvarado, S. G., Tajerian, M., Suderman, M. J., Machnes, Z. M., Pierfelice, S., Millecamps, M., Stone, L. S., & Szyf, M. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00088 · Cited by 63
TET-catalyzed 5-methylcytosine hydroxylation is dynamically regulated by metabolites
Yang, H., Lin, H., Xu, H., Zhang, L., Cheng, L., Wen, B., Shou, J., Guan, K., Xiong, Y., & Ye, D. (2014) · Cell Research · doi:10.1038/cr.2014.81 · Cited by 61
Epigenetic Changes in Chronic Inflammatory Diseases
Fogel, O., Miceli‐Richard, C., & Tost, J. (2016) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2016.09.003 · Cited by 61
Pharmacoepigenetics and Toxicoepigenetics: Novel Mechanistic Insights and Therapeutic Opportunities
Lauschke, V. M., Barragán, I., & Ingelman‐Sundberg, M. (2017) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-010617-053021 · Cited by 63
Parp1 hyperactivity couples DNA breaks to aberrant neuronal calcium signalling and lethal seizures
Komulainen, E., Badman, J., Rey, S. A., Rulten, S. L., Ju, L., Fennell, K., Kalasová, I., Ilievová, K., McKinnon, P. J., Hanzlíková, H., et al. (2021) · EMBO Reports · doi:10.15252/embr.202051851 · Cited by 63
“In addition, the modified base 5’-hydrox-ymethylcytosine is highly enriched in brain and may generate SSBs as an obligate intermediate of DNA base excision repair, during epigenetic reprogramming (Kriaucionis & Heintz, 2009; Li & Liu, 2011).”
Dynamic reprogramming of 5-hydroxymethylcytosine during early porcine embryogenesis
Cao, Z., Zhou, N., Zhang, Y., Zhang, Y., Wu, R., Li, Y., Zhang, Y., & Li, N. (2013) · Theriogenology · doi:10.1016/j.theriogenology.2013.10.025 · Cited by 60
Terragni, J., Bitinaite, J., Zheng, Y., & Pradhan, S. (2012) · Biochemistry · doi:10.1021/bi2014739 · Cited by 60
Xu, B., Devi, G., & Shao, F. (2015) · Organic & Biomolecular Chemistry · doi:10.1039/c4ob02646b · Cited by 60
Gao, F., Xia, Y., Wang, J., Lin, Z., Ou, Y., Liu, X., Liu, W., Zhou, B., Luo, H., Zhou, B., et al. (2014) · Genome biology · doi:10.1186/s13059-014-0533-9 · Cited by 61
Role of DNA methylation in human age prediction
Goel, N., Karir, P., & Garg, V. K. (2017) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2017.08.012 · Cited by 64
Ing1 functions in DNA demethylation by directing Gadd45a to H3K4me3Preprint
Schäfer, A., Karaulanov, E., Stapf, U., Doederlein, G., & Niehrs, C. (2013) · Genes & Development · doi:10.1101/gad.186916.112 · Cited by 64
Chen, Y., Xu, M., Zhang, J., Ma, J., Gao, M., Zhang, Z., Xu, Y., & Liu, S. (2016) · Advanced Materials · doi:10.1002/adma.201604580 · Cited by 59
Selective and Sensitive Detection of Methylcytosine by Aerolysin Nanopore under Serum Condition
Yu, J., Cao, C., & Long, Y. (2017) · Analytical Chemistry · doi:10.1021/acs.analchem.7b03133 · Cited by 60
Ji, P., Wang, X., Xie, N., & Li, Y. (2018) · Stem Cells International · doi:10.1155/2018/3256524 · Cited by 62
Molecular mechanisms of psychiatric diseases
Blokhin, I. O., Khorkova, O., Saveanu, R. V., & Wahlestedt, C. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.105136 · Cited by 64
“DNA demethylation is carried out by the TET methylcytosine dioxygenases (71-74).”
The Application of Next Generation Sequencing in DNA Methylation Analysis
Zhang, Y., & Jeltsch, A. (2010) · Genes · doi:10.3390/genes1010085 · Cited by 60
Chemistry of nucleic acids: impacts in multiple fields
Khakshoor, O., & Kool, E. T. (2011) · Chemical Communications · doi:10.1039/c1cc11021g · Cited by 59
Robertson, J., Robertson, A. B., & Klungland, A. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.06.077 · Cited by 59
Epigenetic mechanisms involved in developmental nutritional programming
Gabory, A. (2011) · World Journal of Diabetes · doi:10.4239/wjd.v2.i10.164 · Cited by 66
Environmental enrichment modulates 5-hydroxymethylcytosine dynamics in hippocampus
Irier, H. A., Street, R. C., Dave, R., Lin, L., Cai, C. W., Davis, T., Yao, B., Cheng, Y., & Jin, P. (2014) · Genomics · doi:10.1016/j.ygeno.2014.08.019 · Cited by 59
Goodman, J. I., Augustine, K. A., Cunnningham, M. L., Dixon, D., Dragan, Y. P., Falls, J. G., Rasoulpour, R. J., Sills, R. C., Storer, R. D., Wolf, D. C., et al. (2010) · Toxicological Sciences · doi:10.1093/toxsci/kfq133 · Cited by 59
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Shu, L., Sun, W., Li, L., Xu, Z., Lin, L., Xie, P., Shen, H., Huang, L., Xu, Q., Jin, P., et al. (2016) · BMC Genomics · doi:10.1186/s12864-016-2731-1 · Cited by 59
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Hoffmann, A., Sportelli, V., Ziller, M. J., & Spengler, D. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18081711 · Cited by 65
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Feng, J., Pena, C. J., Purushothaman, I., Engmann, O., Walker, D., Brown, A. N., Issler, O., Doyle, M., Harrigan, E., Mouzon, E., et al. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2017.6 · Cited by 58
Zhang, M., Wang, J., Zhang, K., Lu, G., Liu, Y., Ren, K., Wang, W., Xin, D. E., Xu, L., Mao, H., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-25353-5 · Cited by 61
Sultan, F. A., & Sweatt, J. D. (2013) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-8289-5_6 · Cited by 58
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Lister, R., & Mukamel, E. A. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00252 · Cited by 62
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Münzel, M., Globisch, D., Trindler, C., & Carell, T. (2010) · Organic Letters · doi:10.1021/ol102408t · Cited by 58
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Bird, A. P. (2011) · Journal of Molecular Biology · doi:10.1016/j.jmb.2011.01.056 · Cited by 60
Massart, R., Suderman, M. J., Provençal, N., Yi, C., Bennett, A. J., Suomi, S. J., & Szyf, M. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.03.021 · Cited by 58
Liu, S., Jiang, J., Li, L., Amato, N. J., Wang, Z., & Wang, Y. (2015) · Environmental Science & Technology · doi:10.1021/acs.est.5b03386 · Cited by 58
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Thomson, J. P., & Meehan, R. R. (2016) · Epigenomics · doi:10.2217/epi-2016-0122 · Cited by 60
Lv, H., Dao, F., Zhang, D., Yang, H. Q., & Lin, H. (2021) · Biotechnology and Bioengineering · doi:10.1002/bit.27911 · Cited by 60
Jordi, E., Heiman, M., Marion-Poll, L., Guermonprez, P., Cheng, S. K., Nairn, A. C., Greengard, P., & Girault, J.-A. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1307116110 · Cited by 57
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Fan, H., Zhang, H., Pascuzzi, P. E., & ANDRISANI, O. M. (2015) · Oncogene · doi:10.1038/onc.2015.122 · Cited by 57
Metadata
- Authors
- Kriaucionis, S., & Heintz, N.
- Affiliations
- Laboratory of Molecular Biology, Howard Hughes Medical Institute, The Rockefeller University, New York, NY 10065, USA.
- Howard Hughes Medical Institute (US)
- Corresponding author
- Heintz, Nathaniel
- ORCID
- Heintz, Nathaniel
- Venue
- Science
- Published
- 2009-05-15
- Volume
- 324
- Issue
- 5929
- Pages
- 929-930
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC3263819
- OpenAlex
- W2152451432
- Cited by
- 2,700
- References
- 14
- Citations by year
- 2026: 53 · 2025: 69 · 2024: 84 · 2023: 93 · 2022: 112 · 2021: 137 · 2020: 107 · 2019: 150 · 2018: 190 · 2017: 218 · 2016: 236 · 2015: 220 · 2014: 259 · 2013: 252 · 2012: 202
- FWCI
- 69.99
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Howard Hughes Medical Institute
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA modifications and cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA and Nucleic Acid Chemistry
- Keywords
- 5-hydroxymethylcytosine, Purkinje cells, cerebellar granule cells, DNA methylation, epigenetic regulation, brain DNA, nucleotide composition
- MeSH terms
- Animals, Brain Chemistry, Cell Line, Cerebellum, Chromatography, High Pressure Liquid, Chromatography, Thin Layer, Cytosine, Deoxycytidine, DNA, DNA Damage, Humans, Purkinje Cells, Mass Spectrometry, 5-Methylcytosine, Mice
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