In vivo targeting of de novo DNA methylation by histone modifications in yeast and mouse
Open accessAbstract
Methylation of cytosines (5meC) is a widespread heritable DNA modification. During mammalian development, two global demethylation events are followed by waves of de novo DNA methylation. In vivo mechanisms of DNA methylation establishment are largely uncharacterized. Here, we use Saccharomyces cerevisiae as a system lacking DNA methylation to define the chromatin features influencing the activity of the murine DNMT3B. Our data demonstrate that DNMT3B and H3K4 methylation are mutually exclusive and that DNMT3B is co-localized with H3K36 methylated regions. In support of this observation, DNA methylation analysis in yeast strains without Set1 and Set2 shows an increase of relative 5meC levels at the transcription start site and a decrease in the gene-body, respectively. We extend our observation to the murine male germline, where H3K4me3 is strongly anti-correlated while H3K36me3 correlates with accelerated DNA methylation. These results show the importance of H3K36 methylation for gene-body DNA methylation in vivo.
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
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?
Patterns of DNA methyltransferase localization, DNA methylation, and actively transcribed gene bodies may be specified by histone modifications.
“studies have suggested that the patterns of DNA methyltransferase localization, DNA methylation, and actively transcribed gene bodies may be specified by histone modifications.113,114”
From Epigenetic regulation in major depression and other stress-related disorders: molecular mechanisms, clinical relevance and therapeutic potential (2023) · cites this paper as [114]
Establishment of intragenic 5mC is a controlled process carried out by DNMT3B and the co-transcriptionally regulated histone modification H3K36me.
“Studies with mESC and a heterologous yeast system found that the establishment of intragenic 5mC is a controlled process carried out by de novo DNA methyltransferase DNMT3B and co-transcriptionally regulated histone modification H3K36me (32, 33).”
From Dynamic DNA methylation: In the right place at the right time (2018) · cites this paper as [33]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
STAR: ultrafast universal RNA-seq aligner
Dobin, A., Davis, C. A., Schlesinger, F., Drenkow, J., Zaleski, C., Jha, S., Batut, P., Chaisson, M., & Gingeras, T. R. (2013) · Bioinformatics · doi:10.1093/bioinformatics/bts635 · Cited by 51,709 · see citing works
Analyzing real-time PCR data by the comparative CT method
Schmittgen, T. D., & Livak, K. J. (2008) · Nature Protocols · doi:10.1038/nprot.2008.73 · Cited by 26,190 · see citing works
Ultrafast and memory-efficient alignment of short DNA sequences to the human genome.
Langmead, B., Trapnell, C., Pop, M., & Salzberg, S. L. (2009) · Genome Biology · doi:10.1186/gb-2009-10-3-r25 · Cited by 21,849 · cited 2× · see citing works
“8 (Langmead et al., 2009) against the sacCer3 genome assembly, allowing up to two mismatches.”
BackgroundMethodDifferential expression analysis for sequence count data
Anders, S., & Huber, W. (2010) · Genome Biology · doi:10.1186/gb-2010-11-10-r106 · Cited by 15,581 · see citing works
Human DNA methylomes at base resolution show widespread epigenomic differences
Lister, R., Pelizzola, M., Dowen, R. H., Hawkins, R. D., Hon, G., Tonti-Filippini, J., Nery, J. R., Lee, L., Ye, Z., Ngo, Q.-M., et al. (2009) · Nature · doi:10.1038/nature08514 · Cited by 4,673 · see citing works
Establishing, maintaining and modifying DNA methylation patterns in plants and animals
Law, J. A., & Jacobsen, S. E. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2719 · Cited by 3,868 · see citing works
Self-citationDNA methylation: roles in mammalian development
Smith, Z. D., & Meissner, A. (2013) · Nature Reviews Genetics · doi:10.1038/nrg3354 · Cited by 3,045 · see citing works
High-efficiency yeast transformation using the LiAc/SS carrier DNA/PEG method
Gietz, R. D., & Schiestl, R. H. (2007) · Nature Protocols · doi:10.1038/nprot.2007.13 · Cited by 2,785 · see citing works
In vitro reprogramming of fibroblasts into a pluripotent ES-cell-like state
Wernig, M., Meissner, A., Foreman, R. K., Brambrink, T., Ku, M., Hochedlinger, K., Bernstein, B., & Jaenisch, R. (2007) · Nature · doi:10.1038/nature05944 · Cited by 2,669 · cited 1× · see citing works
“Mice Mice homozygous for a characterized Oct4-IRES-GFP allele (Wernig et al., 2007) were used for murine H3K36me3 ChIP.”
MethodDNMT3L connects unmethylated lysine 4 of histone H3 to de novo methylation of DNA
Ooi, S. K. T., Qiu, C., Bernstein, E., Li, K., Jia, D., Yang, Z., Erdjument‐Bromage, H., Tempst, P., Lin, S., Allis, C. D., et al. (2007) · Nature · doi:10.1038/nature05987 · Cited by 1,558 · see citing works
Chromosomal Instability and Tumors Promoted by DNA Hypomethylation
Eden, A., Gaudet, F., Waghmare, A., & Jaenisch, R. (2003) · Science · doi:10.1126/science.1083557 · Cited by 1,401 · see citing works
Conservation and divergence of methylation patterning in plants and animals
Feng, S., Cokus, S. J., Zhang, X., Chen, P.-Y., Bostick, M., Goll, M. G., Hetzel, J., Jain, J., Strauss, S. H., Halpern, M. E., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1002720107 · Cited by 1,285 · cited 1× · see citing works
“Preferential methylation of gene bodies over intergenic regions is observed for invertebrates such as honey bees (Apis mellifera), sea squirts (Ciona intestinalis), sea anemones (Nematostella vectensis) (Zemach and Grafi, 2003; Feng et al., 2010).”
BackgroundSelf-citationCancer Genetics and Epigenetics: Two Sides of the Same Coin?
You, J. S., & Jones, P. A. (2012) · Cancer Cell · doi:10.1016/j.ccr.2012.06.008 · Cited by 1,163 · see citing works
The Dynamics of Genome-wide DNA Methylation Reprogramming in Mouse Primordial Germ Cells
Seisenberger, S., Andrews, S., Krueger, F., Arand, J., Walter, J., Santos, F., Popp, C., Thienpont, B., Dean, W., & Reik, W. (2012) · Molecular Cell · doi:10.1016/j.molcel.2012.11.001 · Cited by 973 · cited 5× · see citing works
“5 DNA methylation data from published sources (Seisenberger et al., 2012).”
BackgroundMethodInfluentialUnderstanding the language of Lys36 methylation at histone H3
Wagner, E. J., & Carpenter, P. B. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3274 · Cited by 933 · see citing works
TETonic shift: biological roles of TET proteins in DNA demethylation and transcription
Pastor, W. A., Aravind, L., & Rao, A. (2013) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3589 · Cited by 897 · see citing works
Self-citationGenome-wide erasure of DNA methylation in mouse primordial germ cells is affected by AID deficiency
Popp, C., Dean, W., Feng, S., Cokus, S. J., Andrews, S., Pellegrini, M. A., Jacobsen, S. E., & Reik, W. (2010) · Nature · doi:10.1038/nature08829 · Cited by 860 · cited 1× · see citing works
“5, almost all DNA methylation has been lost (Popp et al., 2010; Seisenberger et al., 2012).”
BackgroundSelf-citationVermeulen, M., Eberl, H. C., Matarese, F., Marks, H., Denissov, S., Butter, F., Lee, K. K., Olsen, J. V., Hyman, A. A., Stunnenberg, H. G., et al. (2010) · Cell · doi:10.1016/j.cell.2010.08.020 · Cited by 806 · see citing works
Gene Body-Specific Methylation on the Active X Chromosome
Hellman, A., & Chess, A. J. (2007) · Science · doi:10.1126/science.1136352 · Cited by 732 · cited 1× · see citing works
“In mammalian soma, inactive X-chromosome shows higher promoter methylation, consistent with its silent state, but markedly lower intragenic methylation (Hellman and Chess, 2007).”
BackgroundGenomic profiling of DNA methyltransferases reveals a role for DNMT3B in genic methylation
Baubec, T., Colombo, D. F., Wirbelauer, C., Schmidt, J., Burger, L., Krebs, A. R., Akalin, A., & Schübeler, D. (2015) · Nature · doi:10.1038/nature14176 · Cited by 705 · see citing works
Dynamic CpG island methylation landscape in oocytes and preimplantation embryos
Smallwood, S. A., Tomizawa, S.-I., Krueger, F., Ruf, N., Carli, N., Segonds-Pichon, A., Sato, S., Hata, K., Andrews, S., & Kelsey, G. (2011) · Nature Genetics · doi:10.1038/ng.864 · Cited by 701 · see citing works
Relationship between nucleosome positioning and DNA methylation
Chodavarapu, R. K., Feng, S., Bernatavichute, Y. V., Chen, P., Stroud, H., Yu, Y., Hetzel, J., Kuo, F., Kim, J., Cokus, S. J., et al. (2010) · Nature · doi:10.1038/nature09147 · Cited by 696 · see citing works
Self-citationChromatin modifiers and remodellers: regulators of cellular differentiation
Chen, T., & Dent, S. (2013) · Nature Reviews Genetics · doi:10.1038/nrg3607 · Cited by 613 · see citing works
The Dnmt3a PWWP Domain Reads Histone 3 Lysine 36 Trimethylation and Guides DNA Methylation
Dhayalan, A., Rajavelu, A., Rathert, P., Tamas, R., Jurkowska, R. Z., Ragozin, S., & Jeltsch, A. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.089433 · Cited by 560 · see citing works
Kobayashi, H., Sakurai, T., Imai, M., Takahashi, N., Fukuda, A., Obata, Y., Sato, S., Nakabayashi, K., Hata, K., Sotomaru, Y., et al. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002440 · Cited by 536 · cited 1× · see citing works
“5 PGCs, actively transcribed gene bodies have far higher levels of DNA methylation than less transcribed genes and intergenic regions (Smallwood et al., 2011; Kobayashi et al., 2012).”
BackgroundA map of nucleosome positions in yeast at base-pair resolution
Brogaard, K., Xi, L., Wang, J.-P., & Widom, J. (2012) · Nature · doi:10.1038/nature11142 · Cited by 452 · see citing works
Reprogramming DNA methylation in the mammalian life cycle: building and breaking epigenetic barriers
Seisenberger, S., Peat, J. R., Hore, T. A., Santos, F., Dean, W., & Reik, W. (2012) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2011.0330 · Cited by 452 · see citing works
Collart, M. A., & Oliviero, S. (1993) · Current Protocols in Molecular Biology · doi:10.1002/0471142727.mb1312s23 · Cited by 451 · cited 1× · see citing works
“Yeast RNA-seq libraries preparation RNA was collected from 5 OD of yeast cells (Collart and Oliviero, 2001).”
MethodThe role of genomic imprinting in biology and disease: an expanding view
Peters, J. (2014) · Nature Reviews Genetics · doi:10.1038/nrg3766 · Cited by 432 · see citing works
BS-Seeker2: a versatile aligning pipeline for bisulfite sequencing data
Guo, W., Fiziev, P. P., Yan, W., Cokus, S. J., Sun, X., Zhang, M. Q., Chen, P., & Pellegrini, M. A. (2013) · BMC Genomics · doi:10.1186/1471-2164-14-774 · Cited by 422 · cited 1× · see citing works
“3 (Guo et al., 2013) against the sacCer3 and mm9 genome assemblies, respectively.”
BackgroundSelf-citationDANPOS: Dynamic analysis of nucleosome position and occupancy by sequencingPreprint
Chen, K.-F., Xi, Y., Pan, X.-W., Li, Z.-Y., Kaestner, K., Tyler, J. K., Dent, S., He, X.-W., & Li, W. (2013) · Genome Research · doi:10.1101/gr.142067.112 · Cited by 415 · cited 1× · see citing works
“3 (Chen et al., 2013) subtracting the naked DNA-derived reads from the nucleosomal reads and using the ‘-k1 -e1’ parameters (Supplementary files 1B, 4).”
MethodZhang, Y., Jurkowska, R. Z., Soeroes, S., Rajavelu, A., Dhayalan, A., Bock, I., Rathert, P., Brandt, O., Reinhardt, R., Fischle, W., et al. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq147 · Cited by 405 · see citing works
Structural insight into autoinhibition and histone H3-induced activation of DNMT3A
Guo, X., Wang, L., Li, J., Ding, Z., Xiao, J., Yin, X., He, S., Shi, P., Dong, L., Li, G., et al. (2015) · Nature · doi:10.1038/nature13899 · Cited by 361 · see citing works
Maze, I. S., Noh, K., Soshnev, A. A., & Allis, C. D. (2014) · Nature Reviews Genetics · doi:10.1038/nrg3673 · Cited by 347 · see citing works
Transcription is required for establishment of germline methylation marks at imprinted genesPreprint
Chotalia, M., Smallwood, S. A., Ruf, N., Dawson, C., Lucifero, D., Frontera, M., James, K., Dean, W., & Kelsey, G. (2009) · Genes & Development · doi:10.1101/gad.495809 · Cited by 346 · cited 1× · see citing works
“Transcriptional read-through is a common feature of maternally imprinted loci (Weaver and Bartolomei, 2014) and ablation of an upstream promoter prevents proper methylation of the imprinted Gnas locus (Chotalia et al., 2009).”
BackgroundLong noncoding RNAs: an emerging link between gene regulation and nuclear organization
Quinodoz, S. A., & Guttman, M. (2014) · Trends in Cell Biology · doi:10.1016/j.tcb.2014.08.009 · Cited by 316 · see citing works
Kobayashi, H., Sakurai, T., Miura, F., Imai, M., Mochiduki, K., Yanagisawa, E., Sakashita, A., Wakai, T., Suzuki, Y., Ito, T., et al. (2013) · Genome Research · doi:10.1101/gr.148023.112 · Cited by 273 · see citing works
Identification of functional cooperative mutations of SETD2 in human acute leukemia
Zhu, X., He, F., Zeng, H., Ling, S., Chen, A., Wang, Y., Yan, X., Wei, W., Pang, Y., Cheng, H., et al. (2014) · Nature Genetics · doi:10.1038/ng.2894 · Cited by 248 · cited 1× · see citing works
“Setd2 is also a tumor suppressor mutated frequently in leukemia (Zhu et al., 2014).”
BackgroundNatural History of Eukaryotic DNA Methylation Systems
Iyer, L. M., Abhiman, S., & Aravind, L. (2011) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-387685-0.00002-0 · Cited by 227 · see citing works
Histone H3 lysine 36 methyltransferase Hypb/Setd2 is required for embryonic vascular remodeling
Hu, M., Sun, X., Zhang, Y.-L., Kuang, Y., Hu, C.-Q., Wu, W., Shen, S.-H., Du, T., Li, H., He, F., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0915033107 · Cited by 183 · cited 1× · see citing works
“5 (Hu et al., 2010), while Setd2 are defective for differentiation toward endoderm (Zhang et al.”
BackgroundThe helical periodicity of DNA on the nucleosome
Klug, A., & Lutter, L. C. (1981) · Nucleic Acids Research · doi:10.1093/nar/9.17.4267 · Cited by 166 · see citing works
Lesch, B. J., Dokshin, G. A., Young, R. A., McCarrey, J. R., & Page, D. C. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1315204110 · Cited by 161 · cited 1× · see citing works
“To test this hypothesis, we analyzed published H3K4me3 ChIP-seq data (Lesch et al., 2013) and performed H3K36me3 ChIP-seq on sorted germ cells of pooled E13.”
MethodMORC1 represses transposable elements in the mouse male germline
Pastor, W. A., Stroud, H., Nee, K., Liu, W., Pezić, D., Manakov, S. A., Lee, S. A., Moissiard, G., Zamudio, N., Bourc’his, D., et al. (2014) · Nature Communications · doi:10.1038/ncomms6795 · Cited by 148 · cited 8× · see citing works
“Mouse germ cells purification for ChIP Collection of embryonic testes was performed following institutional approval for appropriate care and use of laboratory animals, according to published protocols (Pastor et al., 2014).”
BackgroundMethodInfluentialSelf-citationAnnotation Transfer for Genomics: Measuring Functional Divergence in Multi-Domain ProteinsPreprint
Hegyi, H., & Gerstein, M. (2001) · Genome Research · doi:10.1101/gr.183801 · Cited by 135 · see citing works
In Vivo Epigenomic Profiling of Germ Cells Reveals Germ Cell Molecular Signatures
Ng, J.-H., Kumar, V., Muratani, M., Kraus, P., Yeo, J.-C., Yaw, L. P., Xue, K., Lufkin, T., Prabhakar, S., & Ng, H. (2013) · Developmental Cell · doi:10.1016/j.devcel.2012.12.011 · Cited by 125 · see citing works
De novo methylation of MMLV provirus in embryonic stem cells: CpG versus non-CpG methylation
Dodge, J. E., Ramsahoye, B. H., Wo, Z. G., Okano, M., & Li, E. (2002) · Gene · doi:10.1016/s0378-1119(02)00469-9 · Cited by 120 · see citing works
Characterization of Arabidopsis thaliana methyl‐CpG‐binding domain (MBD) proteins
Zemach, A., & Grafi, G. (2003) · The Plant Journal · doi:10.1046/j.1365-313x.2003.01756.x · Cited by 119 · cited 2× · see citing works
“Preferential methylation of gene bodies over intergenic regions is observed for invertebrates such as honey bees (Apis mellifera), sea squirts (Ciona intestinalis), sea anemones (Nematostella vectensis) (Zemach and Grafi, 2003; Feng et al., 2010).”
BackgroundHoffman, C. S. (1997) · Current Protocols in Molecular Biology · doi:10.1002/0471142727.mb1311s39 · Cited by 111 · see citing works
The N-terminus of histone H3 is required for de novo DNA methylation in chromatin
Hu, J.-L., Zhou, B. O., Zhang, R.-R., Zhang, K., Zhou, J., & Xu, G.-L. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0905767106 · Cited by 110 · see citing works
Jin, B., Ernst, J., Tiedemann, R. L., Xu, H., Sureshchandra, S., Kellis, M., Dalton, S., Liu, C., Choi, J.-H., & Robertson, K. D. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.10.017 · Cited by 101 · cited 1× · see citing works
“Transcriptional elongation is also correlated with DNA methylation in tumor cells (Jin et al., 2012).”
BackgroundZhang, Y., Xie, S., Zhou, Y., Xie, Y., Liu, P., Sun, M., Xiao, H., Jin, Y., Sun, X., Zhu, C. H., et al. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.08.031 · Cited by 81 · see citing works
Mechanism for epigenetic variegation of gene expression at yeast telomeric heterochromatinPreprint
Kitada, T., Kuryan, B. G., Tran, N., Song, C., Xue, Y., Carey, M., & Grunstein, M. R. (2012) · Genes & Development · doi:10.1101/gad.201095.112 · Cited by 71 · cited 1× · see citing works
“Yeast ChIP-seq libraries preparation Chromatin immunoprecipitation experiments were conducted according to Kitada et al. (2012), with minor modifications.”
MethodReorganization of the host epigenome by a viral oncogenePreprint
Ferrari, R., Su, T., Li, B., Bonora, G., Oberai, A., Chan, Y. Y., Sasidharan, R., Berk, A. J., Pellegrini, M. A., & Kurdistani, S. K. (2012) · Genome Research · doi:10.1101/gr.132308.111 · Cited by 71 · cited 1× · see citing works
“, 2009), then aligned reads were processed according to Ferrari et al. (2012).”
MethodSelf-citationSingh, P., Li, A. X., Tran, D. A., Oates, N., Kang, E.-R., Wu, X., & Szabó, P. E. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.06.004 · Cited by 68 · cited 2× · see citing works
“This is consistent with the observation that genomic regions bearing H3K4 methylation are generally depleted of 5C (Singh et al., 2013).”
BackgroundNanty, L., Carbajosa, G., Heap, G., Ratnieks, F. L. W., van Heel, D. A., Down, T. A., & Rakyan, V. K. (2011) · Genome Research · doi:10.1101/gr.121640.111 · Cited by 65 · cited 1× · see citing works
“across these species, there is a strong correlation between gene-body H3K36me3 in Drosophila melanogaster genes and DNA methylation of homologous gene bodies in other invertebrates (Nanty et al., 2011).”
BackgroundAnsanay, V., Dequin, S., Camarasa, C., Schaeffer, V. H., Grivet, J. P., Blondin, B., Salmon, J.-M., & Barre, P. (1996) · Yeast · doi:10.1002/(sici)1097-0061(19960315)12:3 · Cited by 53 · see citing works
Chromatin regulators of genomic imprinting
Weaver, J. R., & Bartolomei, M. S. (2013) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2013.12.002 · Cited by 48 · see citing works
Genome-Wide Mapping of Nucleosomes in Yeast
Rando, O. J. (2010) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(10)70005-7 · Cited by 40 · see citing works
Vincent, J. J., Li, Z., Lee, S. A., Liu, X., Etter, M. O., Diaz-Perez, S. V., Taylor, S. K., Gkountela, S., Lindgren, A., & Clark, A. T. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028960 · Cited by 30 · cited 1× · see citing works
“Embryonic male germ cells express the GFP marker and can be sorted efficiently (Vincent et al., 2011; Pastor et al., 2014).”
BackgroundSelf-citation
Flagged first, then by citations
Cited by
Sorted by citations
The DNA methyltransferase family: a versatile toolkit for epigenetic regulation
Lyko, F. (2017) · Nature Reviews Genetics · doi:10.1038/nrg.2017.80 · Cited by 1,475 · see citing works
DNA methylation pathways and their crosstalk with histone methylation
Du, J., Johnson, L. M., Jacobsen, S. E., & Patel, D. J. (2015) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm4043 · Cited by 1,000 · see citing works
Self-citationIntragenic DNA methylation prevents spurious transcription initiation
Neri, F., Rapelli, S., Krepelova, A., Incarnato, D., Parlato, C., Basile, G., Maldotti, M., Anselmi, F., & Oliviero, S. (2017) · Nature · doi:10.1038/nature21373 · Cited by 739 · see citing works
Dynamic DNA methylation: In the right place at the right time
Luo, C., Hajkova, P., & Ecker, J. R. (2018) · Science · doi:10.1126/science.aat6806 · Cited by 668 · see citing works
The histone mark H3K36me2 recruits DNMT3A and shapes the intergenic DNA methylation landscape
Weinberg, D. N., Papillon-Cavanagh, S., Chen, H., Yue, Y., Chen, X., Rajagopalan, K. N., Horth, C., McGuire, J. T., Xu, X., Nikbakht, H., et al. (2019) · Nature · doi:10.1038/s41586-019-1534-3 · Cited by 524 · see citing works
Overview of Histone Modification
Zhang, Y., Sun, Z., Jia, J., Du, T., Zhang, N., Tang, Y., Fang, Y., & Fang, D. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-981-15-8104-5_1 · Cited by 495 · see citing works
Efficient targeted DNA methylation with chimeric dCas9–Dnmt3a–Dnmt3L methyltransferase
Stepper, P., Kungulovski, G., Jurkowska, R. Z., Chandra, T., Krueger, F., Reinhardt, R., Reik, W., Jeltsch, A., & Jurkowski, T. P. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw1112 · Cited by 326 · see citing works
Prenatal stress and epigenetics
Cao-Lei, L., de Rooij, S. R., King, S., Matthews, S. G., Metz, G. A. S., Roseboom, T. J., & Szyf, M. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.05.016 · Cited by 230 · see citing works
Yuan, M., Yang, B., Rothschild, G., Mann, J. J., Sanford, L. D., Tang, X., Huang, C., Wang, C., & Zhang, W. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01519-z · Cited by 246 · see citing works
“113,114 Histone acetylation in stress response and neuroplasticity Histone acetylation at lysine residues (mainly including K9, K14, K18, K23, and K27), is commonly linked to the activation of gene transcription.”
BackgroundThe interplay between DNA and histone methylation: molecular mechanisms and disease implications
Li, Y., Chen, X., & Lu, C. (2021) · The EMBO Reports · doi:10.15252/embr.202051803 · Cited by 223 · see citing works
“Similarly, in SETD2-deficient oocytes and NSD1-deficient sperms, in addition to abnormal CpG methylation there is also an “invasion” of H3K27me3 into former H3K36me2/3 territories (Xu et al , 2019; Shirane et al , 2020).”
InfluentialDynamic changes in histone modifications precede de novo DNA methylation in oocytesPreprint
Stewart-Morgan, K. R., Veselovska, L., Kim, J., Huang, J., Saadeh, H., Tomizawa, S.-I., Smallwood, S. A., Chen, T., & Kelsey, G. (2015) · Genes & Development · doi:10.1101/gad.271353.115 · Cited by 209 · see citing works
Allosteric control of mammalian DNA methyltransferases – a new regulatory paradigm
Jeltsch, A., & Jurkowska, R. Z. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw723 · Cited by 200 · see citing works
Dnmt3a and Dnmt3b Associate with Enhancers to Regulate Human Epidermal Stem Cell Homeostasis
Rinaldi, L., Datta, D., Serrat, J., Morey, L., Solanas, G., Avgustinova, A., Blanco, E., Pons, J., Matallanas, D., von Kriegsheim, A., et al. (2016) · Cell stem cell · doi:10.1016/j.stem.2016.06.020 · Cited by 194 · see citing works
Establishment and Functions of DNA Methylation in the Germline
Stewart-Morgan, K. R., Veselovska, L., & Kelsey, G. (2016) · Epigenomics · doi:10.2217/epi-2016-0056 · Cited by 185 · see citing works
Epigenetic Control of Stem Cell Potential during Homeostasis, Aging, and Disease
Beerman, I., & Rossi, D. J. (2015) · Cell stem cell · doi:10.1016/j.stem.2015.05.009 · Cited by 178 · see citing works
“In contrast to the largely antagonistic relationship of H3K27 and H3K4 methylation with DNAmethylation, H3K36me3, a hallmark of transcriptional elongation, appears to directly recruit and interact with de novo DNA methyltransferases (Dhayalan et al., 2010; Morselli et al., 2015).”
Histone Marks in the ‘Driver’s Seat’: Functional Roles in Steering the Transcription Cycle
Gates, L. A., Foulds, C. E., & O’Malley, B. W. (2017) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2017.10.004 · Cited by 169 · see citing works
Tug of war: adding and removing histone lysine methylation in Arabidopsis
Xiao, J. Y., Lee, U.-S., & Wagner, D. (2016) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2016.08.002 · Cited by 176 · see citing works
“SETD2 physically interacts with the elongating (Ser-2 phosphorylated, Ser2P) form of RNA polymerase II [4,39] and is thus recruited co-transcriptionally.”
BackgroundEvolution of DNA Methylome Diversity in Eukaryotes
de Mendoza, A., Lister, R., & Bogdanović, O. (2019) · Journal of Molecular Biology · doi:10.1016/j.jmb.2019.11.003 · Cited by 165 · see citing works
Impact of DNA methylation on 3D genome structure
Buitrago, D., Labrador, M., Arcon, J. P., Lema, R., Flores, O., Esteve‐Codina, A., Blanc, J. M., Villegas, N., Bellido, D., Gut, M. O., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-23142-8 · Cited by 165 · see citing works
SETD2: an epigenetic modifier with tumor suppressor functionality
Li, J., Duns, G., Westers, H., Sijmons, R. H., van den Berg, A., & Kok, K. (2016) · Oncotarget · doi:10.18632/oncotarget.9368 · Cited by 158 · see citing works
Duymich, C. E., Charlet, J., Yang, X., Jones, P. A., & Liang, G. (2016) · Nature Communications · doi:10.1038/ncomms11453 · Cited by 159 · see citing works
Choi, J., Lyons, D. B., Kim, M. Y., Moore, J. D., & Zilberman, D. (2019) · Molecular Cell · doi:10.1016/j.molcel.2019.10.011 · Cited by 152 · see citing works
Human TFIIH Kinase CDK7 Regulates Transcription-Associated Chromatin Modifications
Ebmeier, C. C., Erickson, B., Allen, B. L., Allen, M. A., Kim, H., Fong, N., Jacobsen, J. R., Liang, K., Shilatifard, A., Dowell, R. D., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.07.021 · Cited by 157 · see citing works
Diversity of cytosine methylation across the fungal tree of life
Bewick, A. J., Hofmeister, B. T., Powers, R. A., Mondo, S. J., Grigoriev, I. V., James, T. Y., Stajich, J., & Schmitz, R. J. (2019) · Nature Ecology & Evolution · doi:10.1038/s41559-019-0810-9 · Cited by 146 · see citing works
Shirane, K., Miura, F., Ito, T., & Lorincz, M. C. (2020) · Nature Genetics · doi:10.1038/s41588-020-0689-z · Cited by 157 · see citing works
Understanding the interplay between CpG island-associated gene promoters and H3K4 methylation
Hughes, A. L., Kelley, J. R., & Klose, R. J. (2020) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2020.194567 · Cited by 139 · see citing works
The preconception environment and sperm epigenetics
Marcho, C., Oluwayiose, O. A., & Pilsner, J. R. (2020) · Andrology · doi:10.1111/andr.12753 · Cited by 147 · see citing works
Interplay between chromatin marks in development and disease
Janssen, S. M., & Lorincz, M. C. (2021) · Nature Reviews Genetics · doi:10.1038/s41576-021-00416-x · Cited by 141 · see citing works
TET Enzymes and 5hmC in Adaptive and Innate Immune Systems
Lio, C. J., & Rao, A. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00210 · Cited by 139 · see citing works
The essential and multifunctional TFIIH complex
Rimel, J. K., & Taatjes, D. J. (2018) · Protein Science · doi:10.1002/pro.3424 · Cited by 137 · see citing works
Rondelet, G., Maso, T. D., Willems, L., & Wouters, J. (2016) · Journal of Structural Biology · doi:10.1016/j.jsb.2016.03.013 · Cited by 137 · see citing works
Shaping the cellular landscape with Set2/SETD2 methylation
McDaniel, S. L., & Strahl, B. D. (2017) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2517-x · Cited by 125 · see citing works
“In the absence of SETD2, DNA methylation is not properly targeted to transcribed regions in the genome, which has been attributed primarily to the loss of DNMT3b targeting by H3K36me3 [112, 113, 148].”
Protection of CpG islands from DNA methylation is DNA-encoded and evolutionarily conserved
Long, H. K., King, H. W., Patient, R. K., Odom, D. T., & Klose, R. J. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw258 · Cited by 128 · see citing works
The role and mechanisms of DNA methylation in the oocyte
Sendžikaitė, G., & Kelsey, G. (2019) · Essays in Biochemistry · doi:10.1042/ebc20190043 · Cited by 129 · see citing works
King, A., Huang, K. Y., Rubbi, L., Liu, S., Wang, C., Wang, Y., Pellegrini, M. A., & Fan, G. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.08.083 · Cited by 119 · see citing works
Self-citationLewis, S. H., Ross, L., Bain, S. A., Pahita, E., Smith, S. A., Cordaux, R., Miska, E. A., Lenhard, B., Jiggins, F. M., & Sarkies, P. (2020) · PLoS Genetics · doi:10.1371/journal.pgen.1008864 · Cited by 103 · see citing works
DNMT3B Functions: Novel Insights From Human Disease
Gagliardi, M., Strazzullo, M., & Matarazzo, M. R. (2018) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2018.00140 · Cited by 107 · see citing works
A DNMT3A PWWP mutation leads to methylation of bivalent chromatin and growth retardation in mice
Sendžikaitė, G., Hanna, C. W., Stewart-Morgan, K. R., Ivanova, E., & Kelsey, G. (2019) · Nature Communications · doi:10.1038/s41467-019-09713-w · Cited by 109 · see citing works
Developmental windows of susceptibility for epigenetic inheritance through the male germline
Ly, L., Chan, D., & Trasler, J. M. (2015) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2015.07.006 · Cited by 106 · see citing works
“A recent study provides evidence for an interaction between DNMT3b and H3K36me3 in male germ cells, suggesting that this histone mark may target DNA me thylation to specific regions (52).”
A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients
Guéant, J.-L., Chéry, C., Oussalah, A., Nadaf, J., Coelho, D., Josse, T., Flayac, J., Robert, A., Koscinski, I., Gastin, I., et al. (2018) · Nature Communications · doi:10.1038/s41467-017-02306-5 · Cited by 93 · see citing works
“5 testes 29 .”
Gene body DNA methylation conspires with H3K36me3 to preclude aberrant transcription
Teissandier, A., & Bourc’his, D. (2017) · The EMBO Journal · doi:10.15252/embj.201796812 · Cited by 89 · see citing works
“Abrogation of this cross-talk — either by deleting the PWWP domain of DNMT3 or by preventing H3K36me3 deposition through SETD2 depletion — specifically impairs gene body DNA methylation (Baubec et al , 2015; Morselli et al , 2015).”
Epigenetic reprogramming during spermatogenesis and male factor infertility
McSwiggin, H., & O’Doherty, A. (2018) · Reproduction · doi:10.1530/rep-18-0009 · Cited by 84 · see citing works
Epigenetic memory marks determine epiallele stability at loci targeted by de novo DNA methylation
Li, J., Yang, D., Huang, H., Zhang, G., He, L. S., Pang, J., Lozano‐Durán, R., Lang, Z., & Zhu, J. (2020) · Nature Plants · doi:10.1038/s41477-020-0671-x · Cited by 84 · see citing works
A cis-acting mechanism mediates transcriptional memory at Polycomb target genes in mammals
Holoch, D., Wassef, M. A., Lövkvist, C., Zielinski, D., Aflaki, S., Lombard, B., Héry, T., Loew, D., Howard, M., & Margueron, R. (2021) · Nature Genetics · doi:10.1038/s41588-021-00964-2 · Cited by 79 · see citing works
Chen, P., Chu, A., Liao, W., Rubbi, L., Janzen, C., Hsu, F., Thamotharan, S., Ganguly, A., Lam, L., Montoya, D. J., et al. (2017) · Reproductive Sciences · doi:10.1177/1933719117716779 · Cited by 75 · see citing works
“It was also shown that DNMT3b and 5meC are strongly reciprocally correlated with H3K4me3 and positively correlated with H3K36me3.”
BackgroundSelf-citationNucleosome positioning: resources and tools online
Teif, V. B. (2015) · Briefings Bioinform. · doi:10.1093/bib/bbv086 · Cited by 66 · see citing works
Human epigenetic ageing is logarithmic with time across the entire lifespan
Snir, S., Farrell, C. P., & Pellegrini, M. A. (2019) · Epigenetics · doi:10.1080/15592294.2019.1623634 · Cited by 70 · see citing works
Self-citationFu, K., Bonora, G., & Pellegrini, M. A. (2019) · Epigenetics · doi:10.1080/15592294.2019.1666649 · Cited by 69 · see citing works
Self-citationRecurrent acquisition of cytosine methyltransferases into eukaryotic retrotransposons
de Mendoza, A., Bonnet, A., Vargas-Landín, D. B., Ji, N., Li, H., Yang, X., Li, L., Hori, K., Pflueger, J., Buckberry, S., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-03724-9 · Cited by 64 · see citing works
DNA methylation in disease: Immunodeficiency, Centromeric instability, Facial anomalies syndrome
Vukić, M., & Daxinger, L. (2019) · Essays in Biochemistry · doi:10.1042/ebc20190035 · Cited by 64 · see citing works
Dunican, D. S., Mjoseng, H. K., Duthie, L., Flyamer, I. M., Bickmore, W. A., & Meehan, R. R. (2020) · BMC Biology · doi:10.1186/s12915-020-0752-3 · Cited by 66 · see citing works
Setd2 deficiency impairs hematopoietic stem cell self-renewal and causes malignant transformation
Zhang, Y.-L., Sun, J.-W., Xie, Y.-Y., Zhou, Y., Liu, P., Song, J.-C., Xu, C., Wang, L., Liu, D., Xu, A., et al. (2018) · Cell Research · doi:10.1038/s41422-018-0015-9 · Cited by 64 · see citing works
Enzymology of Mammalian DNA Methyltransferases
Jurkowska, R. Z., & Jeltsch, A. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-43624-1_5 · Cited by 56 · see citing works
Rinaldi, L., Avgustinova, A., Martı́n, M., Datta, D., Solanas, G., Prats, N., & Benitah, S. A. (2017) · eLife · doi:10.7554/elife.21697 · Cited by 54 · see citing works
“For instance, Dnmt3b associates with and methylates the gene bodies of actively transcribed genes in murine embryonic SCs and human embryonic carcinoma cells (Baubec et al., 2015; Jin et al., 2012; Morselli et al., 2015).”
BackgroundDevelopmental underpinnings of spermatogonial stem cell establishment
Law, N. C., & Oatley, J. M. (2020) · Andrology · doi:10.1111/andr.12810 · Cited by 55 · see citing works
The role of histone H3K36me3 writers, readers and erasers in maintaining genome stability
Sharda, A., & Humphrey, T. C. (2022) · DNA repair · doi:10.1016/j.dnarep.2022.103407 · Cited by 55 · see citing works
Identification of DNA motifs that regulate DNA methylation
Wang, M., Zhang, K., Ngo, V., Liu, C., Fan, S., Whitaker, J. W., Chen, Y., Ai, R., Chen, Z., Wang, J., et al. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz483 · Cited by 54 · see citing works
Mechanisms of DNA Methylation Regulatory Function and Crosstalk with Histone Lysine Methylation
Tibben, B. M., & Rothbart, S. B. (2023) · Journal of Molecular Biology · doi:10.1016/j.jmb.2023.168394 · Cited by 55 · see citing works
Target specificity of mammalian DNA methylation and demethylation machinery
Ravichandran, M., Jurkowska, R. Z., & Jurkowski, T. P. (2017) · Organic & Biomolecular Chemistry · doi:10.1039/c7ob02574b · Cited by 54 · see citing works
Sun, L., Song, G., Guo, W., Wang, W., HongKun, Z., Gao, T., Lv, Q., Yang, X., Xu, F., Dong, Y., et al. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.01031 · Cited by 54 · see citing works
Epigenetic factors in the regulation of prospermatogonia and spermatogonial stem cells
Tseng, Y., Liao, H., Yu, C.-Y., Mo, C.-F., & Lin, S. (2015) · Reproduction · doi:10.1530/rep-14-0679 · Cited by 53 · see citing works
“5 prospermatogonia, coinciding with redistributing the active marks of H3K4me2/3 and H3K36me3 in prospermatogonia (Singh et al. 2013, Morselli et al. 2015).”
DNMT3A reads and connects histone H3K36me2 to DNA methylation
Xu, W., Li, J., Rong, B., Zhao, B., Wang, M., Dai, R., Chen, Q., Liu, H., Gu, Z., Liu, S., et al. (2019) · Protein & Cell · doi:10.1007/s13238-019-00672-y · Cited by 51 · see citing works
Fine-tuning of gene expression through the Mettl3-Mettl14-Dnmt1 axis controls ESC differentiation
Quarto, G., Li Greci, A., Bizet, M., Penning, A., Primac, I., Murisier, F., Garcia-Martinez, L., Borges, R. L., Gao, Q., Cingaram, P. K. R., et al. (2025) · Cell · doi:10.1016/j.cell.2024.12.009 · Cited by 50 · see citing works
Lanciano, S., Philippe, C., Sarkar, A., Pratella, D., Domrane, C., Doucet, A. J., van Essen, D., Saccani, S., Ferry, L., Defossez, P., et al. (2024) · Cell Genomics · doi:10.1016/j.xgen.2024.100498 · Cited by 50 · see citing works
Switching between Epigenetic States at Pericentromeric Heterochromatin
Déjardin, J. (2015) · Trends in Genetics · doi:10.1016/j.tig.2015.09.003 · Cited by 47 · see citing works
Chromatin-dependent allosteric regulation of DNMT3A activity by MeCP2
Rajavelu, A., Lungu, C., Emperle, M., Dukatz, M., Bröhm, A., Broche, J., Hanelt, I., Parsa, E., Schiffers, S., Karnik, R., et al. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky715 · Cited by 45 · see citing works
Leung, C. S., Douglass, S. M., Morselli, M., Obusan, M. B., Pavlyukov, M. S., Pellegrini, M. A., & Johnson, T. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.05.100 · Cited by 45 · see citing works
Self-citationEpigenetic regulation of prostate cancer: the theories and the clinical implications
Xu, K., & Liao, Y. (2018) · Asian Journal of Andrology · doi:10.4103/aja.aja_53_18 · Cited by 44 · see citing works
Tompkins, J. D., Jung, M., Chen, C.-Y., Lin, Z., Ye, J., Godatha, S., Lizhar, E. M., Wu, X., Hsu, D. S., Couture, L. A., et al. (2016) · EBioMedicine · doi:10.1016/j.ebiom.2016.01.021 · Cited by 44 · see citing works
Setd2 supports GATA3+ST2+ thymic-derived Treg cells and suppresses intestinal inflammation
Ding, Z., Cai, T., Tang, J., Sun, H., Qi, X., Zhang, Y., Ji, Y., Yuan, L., Chang, H., Ma, Y., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-35250-0 · Cited by 41 · see citing works
H3K36 Methylation in Neural Development and Associated Diseases
Zaghi, M., Broccoli, V., & Sessa, A. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2019.01291 · Cited by 41 · see citing works
“Recent work has demonstrated how the process of DNA methylation is tightly regulated and linked with both H3K36me2 and me3 (Baubec et al., 2015; Morselli et al., 2015; Weinberg et al., 2019).”
PHF14 enhances DNA methylation of SMAD7 gene to promote TGF-β-driven lung adenocarcinoma metastasis
Tian, H., Liu, C., Yu, J., Han, J., Du, J., Liang, S., Wang, W., Liu, Q., Lian, R., Zhu, T., et al. (2023) · Cell Discovery · doi:10.1038/s41421-023-00528-0 · Cited by 35 · see citing works
Epigenetic Signaling and Crosstalk in Regulation of Gene Expression and Disease Progression
Manna, S., Mishra, J., Baral, T., Kirtana, R., Nandi, P., Roy, A., Chakraborty, S., Niharika, N., & Patra, S. K. (2023) · Epigenomics · doi:10.2217/epi-2023-0235 · Cited by 33 · see citing works
KRAB zinc finger protein diversification drives mammalian interindividual methylation variability
Bertozzi, T. M., Elmer, J. L., Macfarlan, T. S., & Ferguson‐Smith, A. C. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2017053117 · Cited by 33 · see citing works
Transposon-associated epigenetic silencing during Pleurotus ostreatus life cycle
Borgognone, A., Castanera, R., Morselli, M., López-Varas, L., Rubbi, L., Pisabarro, A. G., Pellegrini, M. A., & Ramı́rez, L. (2018) · DNA Research · doi:10.1093/dnares/dsy016 · Cited by 32 · see citing works
“Whole genome bisulphite (WGBS) libraries were prepared as described in Morselli et al. 39 Briefly, genomic DNA (gDNA) from the fungal samples was extracted using an E.Z.N.A Fungal DNA Mini Kit (Omega Bio-Tek, Norcross, GA).”
Self-citationInsight into origins, mechanisms, and utility of DNA methylation in B-cell malignancies
Oakes, C. C., & Martín-Subero, J. I. (2018) · Blood · doi:10.1182/blood-2018-02-692970 · Cited by 32 · see citing works
Remodeling the epigenome and (epi)cytoskeleton: a new paradigm for co-regulation by methylation
Walker, C. L., & Burggren, W. W. (2020) · Journal of Experimental Biology · doi:10.1242/jeb.220632 · Cited by 31 · see citing works
Misregulation of the expression and activity of DNA methyltransferases in cancer
Mensah, I. K., Norvil, A. B., AlAbdi, L., McGovern, S. E., Petell, C. J., He, M., & Gowher, H. (2021) · NAR Cancer · doi:10.1093/narcan/zcab045 · Cited by 33 · see citing works
Wong, C. H., Li, C. H., TONG, J. H. M., Zheng, D., Qi-fang, H., Luo, Z., Lou, U. K., Wang, J., To, K., & Chen, Y. (2022) · Molecular Therapy · doi:10.1016/j.ymthe.2022.01.038 · Cited by 30 · see citing works
Fetal testis organ culture reproduces the dynamics of epigenetic reprogramming in rat gonocytes
Rwigemera, A., Joao, F., & Delbès, G. (2017) · Epigenetics & Chromatin · doi:10.1186/s13072-017-0127-3 · Cited by 29 · see citing works
Fain, J. S., Loriot, A. E., Diacofotaki, A., Tongelen, A. V., & Smet, C. D. (2021) · Scientific Reports · doi:10.1038/s41598-021-96844-0 · Cited by 29 · see citing works
Perinatal stress and epigenetics.
(2021) · Handbook of Clinical Neurology · doi:10.1016/b978-0-12-820107-7.00008-2 · Cited by 28 · see citing works
Flanking sequence preference modulates de novo DNA methylation in the mouse genome
Mallona, I., Ilie, I. M., Karemaker, I. D., Butz, S., Manzo, M., Caflisch, A., & Baubec, T. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa1168 · Cited by 28 · see citing works
Do social insects support Haig's kin theory for the evolution of genomic imprinting?
Pegoraro, M., Marshall, H., Lonsdale, Z. N., & Mallon, E. B. (2017) · Epigenetics · doi:10.1080/15592294.2017.1348445 · Cited by 26 · see citing works
Maintaining memory of silencing at imprinted differentially methylated regions
Voon, H. P. J., & Gibbons, R. J. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2157-6 · Cited by 27 · see citing works
Toubiana, S., Gagliardi, M., Papa, M., Manco, R., Tzukerman, M., Matarazzo, M. R., & Selig, S. (2019) · eLife · doi:10.7554/elife.47859 · Cited by 25 · see citing works
Methylation-Demethylation Dynamics: Implications of Changes in Acute Kidney Injury
Chakraborty, A., & Viswanathan, P. (2018) · Analytical Cellular Pathology · doi:10.1155/2018/8764384 · Cited by 25 · see citing works
“[100] showed that in Saccharomyces cerevisiae that expressed a heterologous DNMT3b or in mouse ES cells, DNMT3b is specifically enriched at H3K36me3 sites and that recruitment is based on binding affinity.”
BackgroundSeparovich, R. J., & Wilkins, M. R. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.100939 · Cited by 25 · see citing works
ZMYM2 is essential for methylation of germline genes and active transposons in embryonic development
Graham-Paquin, A.-L., Saini, D., Sirois, J., Hossain, I., Katz, M. S., Zhuang, Q. K.-W., Kwon, S. Y., Yamanaka, Y., Bourque, G., Bouchard, M., et al. (2023) · Nucleic Acids Research · doi:10.1093/nar/gkad540 · Cited by 24 · see citing works
Self-citationEpigenetic Mechanisms Governing Female and Male Germline Development in Mammals
Shirane, K., & Lorincz, M. C. (2022) · Sexual Development · doi:10.1159/000529336 · Cited by 24 · see citing works
“5 [Morselli et al., 2015].”
Magwanga, R. O., Kirungu, J. N., Lu, P., Cai, X., Zhou, Z., Xu, Y., Hou, Y., Agong, S. G., Wang, K., & Liu, F. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20194953 · Cited by 22 · see citing works
Setd2 determines distinct properties of intestinal ILC3 subsets to regulate intestinal immunity
Chang, J., Ji, X., Deng, T., Qiu, J., Ding, Z., Li, Z., Ma, Y., Hu, X., Li, L., & Qiu, J. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110530 · Cited by 20 · see citing works
Finnegan, A., Kim, S., Jin, H., Gapinske, M., Woods, W. S., Pérez‐Piñera, P., & Song, J. S. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa161 · Cited by 20 · see citing works
Epigenetic and epitranscriptomic regulation of axon regeneration
Cheng, Y., Song, H., Ming, G., & Weng, Y. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02028-9 · Cited by 20 · see citing works
Recognition of cancer mutations in histone H3K36 by epigenetic writers and readers
Klein, B. J., Krajewski, K., Restrepo, S., Lewis, P. W., Strahl, B. D., & Kutateladze, T. G. (2018) · Epigenetics · doi:10.1080/15592294.2018.1503491 · Cited by 20 · see citing works
Liu, D.-J., Zhang, F., Chen, Y., Jin, Y., Zhang, Y., Chen, S.-B., Xie, Y., Huang, Q., Zhao, W., Wang, L., et al. (2020) · Cell Discovery · doi:10.1038/s41421-020-00203-8 · Cited by 19 · see citing works
The Absence of C-5 DNA Methylation in Leishmania donovani Allows DNA Enrichment from Complex Samples
Cuypers, B., Dumetz, F., Meysman, P., Laukens, K., Muylder, G. D., Dujardin, J., & Domagalska, M. A. (2020) · Microorganisms · doi:10.3390/microorganisms8081252 · Cited by 19 · see citing works
Lea, G., Doria-Borrell, P., Ferrero-Micó, A., Varma, A., Simon, C. S., Anderson, H., Biggins, L., Clercq, K. D., Andrews, S., Niakan, K. K., et al. (2025) · Cell stem cell · doi:10.1016/j.stem.2024.12.007 · Cited by 19 · see citing works
NSD3: Advances in cancer therapeutic potential and inhibitors research
Xiu, S., Chi, X., Jia, Z., Cheng, S., Zhang, X., Li, Q., Gao, T., Zhang, L., & Liu, Z. (2023) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2023.115440 · Cited by 18 · see citing works
Zhang, L., Rong, W., Ma, J., Li, H., Tang, X., Xu, S., Wang, L., Wan, L., Zhu, Q. C., Jiang, B., et al. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.827391 · Cited by 17 · see citing works
- Authors
- Morselli, M., Pastor, W. A., Montanini, B., Nee, K., Ferrari, R., Fu, K., Bonora, G., Rubbi, L., Clark, A. T., Ottonello, S., Jacobsen, S. E., & Pellegrini, M.
- Affiliations
- University of California, Los Angeles (US)
- University of Parma (IT)
- Howard Hughes Medical Institute (US)
- Corresponding author
- Morselli, Marco
- Jacobsen, Steven E
- Pellegrini, Matteo
- ORCID
- Venue
- eLife
- Publisher
- eLife Sciences Publications, Ltd
- Published
- 2015-04-07
- Volume
- 4
- Pages
- e06205-e06205
- ISSN
- 2050-084X (ISSN-L)
- PMC
- PMC4412109
- OpenAlex
- W2087785865
- Cited by
- 167
- References
- 59
- Citations by year
- 2026: 7 · 2025: 9 · 2024: 11 · 2023: 17 · 2022: 10 · 2021: 16 · 2020: 19 · 2019: 22 · 2018: 16 · 2017: 17 · 2016: 13 · 2015: 10
- FWCI
- 8.10
- Type
- journal article
- Language
- en
- Update notices
- correction (2017-08-31)
- Open access
- gold
- doi.org
- Licence
- Locations
- eLife (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Institutional Research Information System University of Ferrara (University of Ferrara) (submittedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- eScholarship (California Digital Library) (submittedVersion)
- eScholarship (California Digital Library) (submittedVersion, cc-by)
- Funders
- National Institutes of Health (NIH) (R01 GM095656-01A1, GM60398)
- National Institute of Child Health and Human Development (NICHD) (R01HD058047)
- Howard Hughes Medical Institute (HHMI)
- Jane Coffin Childs Memorial Fund for Medical Research
- Whitcome Fellowship
- 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
- de novo methylation, histone modifications, DNMT3B, H3K4 methylation, H3K36 methylation, Saccharomyces cerevisiae, Set1, Set2, gene body methylation, transcription start sites, male germline, chromatin
- MeSH terms
- DNA Methyltransferase 3B, Animals, Chromatin, Cytosine, DNA (Cytosine-5-)-Methyltransferases, Embryo, Mammalian, Genetic Vectors, Germ Cells, Histones, Male, Methyltransferases, Histone-Lysine N-Methyltransferase, Saccharomyces cerevisiae, Transformation, Genetic, Signal Transduction, Open Reading Frames, Gene Expression Regulation, Developmental, CpG Islands, DNA Methylation, Protein Isoforms, Transcription Initiation Site, Saccharomyces cerevisiae Proteins, Mice
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