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Impact of cytosine methylation on DNA binding specificities of human transcription factors
Open accessAbstract
Positives and negatives of methylated CpG: When the DNA bases cytosine and guanine are next to each other, a methyl group is generally added to the pyrimidine, generating a mCpG dinucleotide. This modification alters DNA structure but can also affect function by inhibiting transcription factor (TF) binding. Yin et al. systematically analyzed the effect of CpG methylation on the binding of 542 human TFs (see the Perspective by Hughes and Lambert). In addition to inhibiting binding of some TFs, they found that mCpGs can promote binding of others, particularly TFs involved in development, such as homeodomain proteins. Science , this issue p. eaaj2239 ; see also p. 489
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“Of interest, the HNF4A binding motif does not contain a CG which can be methylated, thus making it a methylation-insensitive TF (11, 17).”
From Hepatocyte Nuclear Factor 4‐Alpha Is Essential for the Active Epigenetic State at Enhancers in Mouse Liver (2019) · cites this paper as [17]
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“Although many TF, including several members of the ETS family, display reduced binding affinities to DNA motifs containing methylated cytosine residues (44)”
From PU.1-Dependent Enhancer Inhibition Separates Tet2 -Deficient Hematopoiesis from Malignant Transformation (2022) · cites this paper as [44]
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“Given that the affinity of many transcription factors, including CTCF31, is negatively impacted by methylation of their binding sites32, it is possible that hypermethylation of DMR_394 disrupts binding of regulatory proteins and adversely affects the organization and regulation of genes nearby.”
From Integrated analysis of behavioral, epigenetic, and gut microbiome analyses in AppNL-G-F, AppNL-F, and wild type mice (2021) · cites this paper as [32]
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“DNA methylation (5-methylcytosine or 5mC) is associated with gene repression (16) and can disrupt the binding of many TFs (17, 18).”
From Hepatocyte Nuclear Factor 4‐Alpha Is Essential for the Active Epigenetic State at Enhancers in Mouse Liver (2019) · cites this paper as [17]
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“These studies unexpectedly uncovered that certain interactions between TFs and low affinity binding sites can be enhanced by the presence of 5mC.”
From Dynamic DNA methylation: In the right place at the right time (2018) · cites this paper as [28]
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Cites
Fast and accurate short read alignment with Burrows-Wheeler transform
Li, H., & Durbin, R. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp324 · Cited by 58,607
Fast gapped-read alignment with Bowtie 2
Langmead, B., & Salzberg, S. L. (2012) · Nature Methods · doi:10.1038/nmeth.1923 · Cited by 56,400
Coot : model-building tools for molecular graphics
Emsley, P., & Cowtan, K. (2004) · Acta Crystallographica Section D Biological Crystallography · doi:10.1107/s0907444904019158 · Cited by 30,571
Features and development of Coot
Emsley, P., Lohkamp, B., Scott, W. G., & Cowtan, K. (2010) · Acta Crystallographica Section D Biological Crystallography · doi:10.1107/s0907444910007493 · Cited by 29,915
Takahashi, K., & Yamanaka, S. (2006) · Cell · doi:10.1016/j.cell.2006.07.024 · Cited by 26,673
PHENIX : a comprehensive Python-based system for macromolecular structure solution
Adams, P. D., Afonine, P. V., Bunkóczi, G., Chen, V. B., Davis, I. W., Echols, N., Headd, J. J., Hung, L.-W., Kapral, G. J., Grosse-Kunstleve, R. W., et al. (2010) · Acta Crystallographica Section D Biological Crystallography · doi:10.1107/s0907444909052925 · Cited by 23,716
Phaser crystallographic software
McCoy, A. J., Grosse-Kunstleve, R. W., Adams, P. D., Winn, M. D., Storoni, L. C., & Read, R. J. (2007) · Journal of Applied Crystallography · doi:10.1107/s0021889807021206 · Cited by 20,612
Model-based Analysis of ChIP-Seq (MACS)
Zhang, Y., Liu, T., Meyer, C. A., Eeckhoute, J., Johnson, D. S., Bernstein, B. E., Nusbaum, C., Myers, R. M., Brown, M., Li, W., et al. (2008) · Genome Biology · doi:10.1186/gb-2008-9-9-r137 · Cited by 18,386
Kabsch, W. (2010) · Acta Crystallographica Section D Biological Crystallography · doi:10.1107/s0907444909047337 · Cited by 16,463
Overview of the CCP 4 suite and current developments
Winn, M. D., Ballard, C. C., Cowtan, K. D., Dodson, E. J., Emsley, P., Evans, P. R., Keegan, R. M., Krissinel, E. B., Leslie, A. G. W., McCoy, A., et al. (2011) · Acta Crystallographica Section D Biological Crystallography · doi:10.1107/s0907444910045749 · Cited by 12,353
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Policarpi, C., Dabin, J., & Hackett, J. A. (2021) · BioEssays · doi:10.1002/bies.202000316 · Cited by 54
Zhong, F., Lin, Y., Zhao, L., Yang, C., Ye, Y., & Shen, Z. (2023) · British Journal of Cancer · doi:10.1038/s41416-023-02292-0 · Cited by 58
Self-citationWang, C., Li, J., Chen, J., Wang, Z., Zhu, G., Song, L., Wu, J., Li, C., Qiu, R., Chen, X., et al. (2025) · Nature Communications · doi:10.1038/s41467-024-55068-2 · Cited by 59
Yadav, D. K., Shrestha, S., Lillycrop, K. A., Joglekar, C. V., Pan, H., Holbrook, J. D., Fall, C. H. D., Yajnik, C. S., & Chandak, G. R. (2017) · Epigenomics · doi:10.2217/epi-2017-0102 · Cited by 57
Leung, K., Nguyen, A. N., Shi, T., Tang, L., Ni, X., Escoubet, L., MacBeth, K. J., DiMartino, J. F., & Wells, J. A. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1813666116 · Cited by 56
Tobi, E. W., van den Heuvel, J., Zwaan, B. J., Lumey, L. H., Heijmans, B. T., & Uller, T. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.11.023 · Cited by 58
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Novakovsky, G., Fornés, O., Saraswat, M., Mostafavi, S., & Wasserman, W. W. (2023) · Genome biology · doi:10.1186/s13059-023-02985-y · Cited by 64
Bogan, S. N., & Yi, S. V. (2024) · Genome Biology and Evolution · doi:10.1093/gbe/evae022 · Cited by 60
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Gonseth, S., Shaw, G. M., Roy, R., Segal, M. R., Asrani, K., Rine, J., Wiemels, J. L., & Marini, N. J. (2019) · Epigenetics · doi:10.1080/15592294.2019.1581591 · Cited by 52
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Achinger-Kawecka, J., Stirzaker, C., Portman, N., Campbell, E. M., Chia, K.-M., Du, Q., Laven‐Law, G., Nair, S. S., Yong, A., Wilkinson, A., et al. (2024) · Nature Structural & Molecular Biology · doi:10.1038/s41594-023-01181-7 · Cited by 46
TFBSshape: an expanded motif database for DNA shape features of transcription factor binding sites
Chiu, T.-P., Xin, B., Markarian, N., Wang, Y., & Rohs, R. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz970 · Cited by 41
EpiMethylTag: simultaneous detection of ATAC-seq or ChIP-seq signals with DNA methylation
Lhoumaud, P., Sethia, G., Izzo, F., Sakellaropoulos, T., Snetkova, V., Vidal, S. E., Badri, S., Cornwell, M., Giammartino, D. C. D., Kim, K., et al. (2019) · Genome biology · doi:10.1186/s13059-019-1853-6 · Cited by 41
Stevens, M. L., Zhang, Z., Johansson, E., Ray, S., Jagpal, A., Ruff, B. P., Kothari, A., He, H., Martin, L. J., Ji, H., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-17895-x · Cited by 41
The transcription factor code in iPSC reprogramming
Deng, W., Jacobson, E. C., Collier, A. J., & Plath, K. (2021) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2021.06.003 · Cited by 43
Lemma, R. B., Fleischer, T., Martinsen, E., Ledsaak, M., Kristensen, V. N., Eskeland, R., Gabrielsen, O. S., & Mathelier, A. (2022) · Epigenetics & Chromatin · doi:10.1186/s13072-022-00444-9 · Cited by 47
DNA Methylation Atlas of the Mouse Brain at Single-Cell Resolution
Liu, H., Zhou, J., Tian, W., Luo, C., Bartlett, A., Aldridge, A., Lucero, J., Osteen, J. K., Nery, J. R., Chen, H., et al. (2020) · doi:10.1101/2020.04.30.069377 · Cited by 290
The epigenetics of animal personality
van Oers, K., van den Heuvel, K., & Sepers, B. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105194 · Cited by 41
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Koijam, A. S., Singh, K. D., Singh, N. B., Haobam, R., & Rajashekar, Y. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115951 · Cited by 45
Rowland, T. J., Bonham, A. J., & Cech, T. R. (2020) · Molecular Oncology · doi:10.1002/1878-0261.12786 · Cited by 41
The methylation landscape and its role in domestication and gene regulation in the chicken
Höglund, A., Henriksen, R., Fogelholm, J., Churcher, A. M., Guerrero‐Bosagna, C., Barrio, Á. M., Johnsson, M., Jensen, P., & Wright, D. (2020) · Nature Ecology & Evolution · doi:10.1038/s41559-020-01310-1 · Cited by 41
Detection of Circulating Tumor DNA Methylation in Diagnosis of Colorectal Cancer
Xu, F., Yu, S., Han, J., Zong, M., Tan, Q., Zeng, X. Y., & Fan, L. (2021) · Clinical and Translational Gastroenterology · doi:10.14309/ctg.0000000000000386 · Cited by 40
Zhang, W., Young, J. I., Gomez, L., Schmidt, M. A., Lukacsovich, D., Varma, A., Chen, X. S., Martin, E. R., & Wang, L. (2023) · Alzheimer s Research & Therapy · doi:10.1186/s13195-023-01216-7 · Cited by 38
Rimoldi, M., Wang, N., Zhang, J., Villar, D., Odom, D. T., Taipale, J., Flicek, P., & Roller, M. (2024) · Genome biology · doi:10.1186/s13059-024-03218-6 · Cited by 42
Self-citationZhao, T., Guan, X., Hu, Y., Zhang, Z., Yang, H., Shi, X., Han, J., Mei, H., Wang, L., Shao, L., et al. (2024) · Cell Research · doi:10.1038/s41422-024-01027-x · Cited by 47
Spatial joint profiling of DNA methylome and transcriptome in tissues
Lee, C. N., Fu, H., Cardilla, A., Zhou, W., & Deng, Y. (2025) · Nature · doi:10.1038/s41586-025-09478-x · Cited by 42
Wallace, R. G., Twomey, L. C., Custaud, M., Turner, J. D., Moyna, N. M., Cummins, P. M., & Murphy, R. P. (2017) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2017.11.013 · Cited by 40
Gatev, E., Inkster, A. M., Negri, G. L., Konwar, C., Lussier, A. A., Skakkebaek, A. H., Sokolowski, M. B., Gravholt, C. H., Dunn, E. C., Kobor, M. S., et al. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkab682 · Cited by 41
Charvin, M., Halter, T., Blanc‐Mathieu, R., Barraud, P., Nicaise, M., Parcy, F., & Navarro, L. (2023) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiad069 · Cited by 39
Roles of the CSE1L-mediated nuclear import pathway in epigenetic silencing
Dong, Q., Li, X., Wang, C., Xu, S., Yuan, G., Shao, W., Liu, B., Zheng, Y., Wang, H., Lei, X., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1800505115 · Cited by 38
Chromatin loops are an ancestral hallmark of the animal regulatory genome
Kim, I. V., Navarrete, C., Grau‐Bové, X., Iglesias, M., Elek, A., Zolotarov, G., Bykov, N. S., Montgomery, S. A., Księżopolska, E., Cañas-Armenteros, D., et al. (2025) · Nature · doi:10.1038/s41586-025-08960-w · Cited by 43
Metadata
- Authors
- Yin, Y., Morgunova, E., Jolma, A., Kaasinen, E., Sahu, B., Khund-Sayeed, S., Das, P. K., Kivioja, T., Dave, K., Zhong, F., Nitta, K. R., Taipale, M., Popov, A., Ginno, P. A., Domcke, S., Yan, J., Schübeler, D., Vinson, C., & Taipale, J.
- Affiliations
- Karolinska Institutet (SE)
- University of Helsinki (FI)
- National Institutes of Health (US)
- European Synchrotron Radiation Facility (FR)
- Friedrich Miescher Institute (CH)
- University of Basel (CH)
- Corresponding author
- Taipale, Jussi
- ORCID
- Venue
- Science
- Published
- 2017-05-05
- Volume
- 356
- Issue
- 6337
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC8009048
- OpenAlex
- W2610903912
- Cited by
- 1,257
- References
- 97
- Citations by year
- 2026: 92 · 2025: 138 · 2024: 148 · 2023: 159 · 2022: 166 · 2021: 150 · 2020: 125 · 2019: 125 · 2018: 113 · 2017: 37
- FWCI
- 44.66
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Academy of Finland Center of Excellence in Cancer Genetics
- European Research Area SynBio
- Center for Innovative Medicine at Karolinska Institutet
- Knut and Alice Wallenberg Foundation
- Göran Gustafsson Foundation
- Vetenskapsrådet
- 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 › Molecular Biology › DNA and Nucleic Acid Chemistry
- Keywords
- cytosine methylation, CpG methylation, transcription factor binding specificity, DNA methylation, homeodomain transcription factor, 5-methylcytosine, hydrophobic interactions, epigenetic regulation, gene regulatory elements
- MeSH terms
- Protein Domains, Cytosine, DNA, Humans, Protein Binding, Transcription Factors, Dinucleoside Phosphates, Genome, Human, CpG Islands, DNA Methylation, Epigenesis, Genetic, SELEX Aptamer Technique
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