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Methyl-CpG-Binding Domain Proteins: Readers of the Epigenome
Open accessAbstract
How DNA methylation is interpreted and influences genome regulation remains largely unknown. Proteins of the methyl-CpG-binding domain (MBD) family are primary candidates for the readout of DNA methylation as they recruit chromatin remodelers, histone deacetylases and methylases to methylated DNA associated with gene repression. MBD protein binding requires both functional MBD domains and methyl-CpGs; however, some MBD proteins also bind unmethylated DNA and active regulatory regions via alternative regulatory domains or interaction with the nucleosome remodeling deacetylase (NuRD/Mi-2) complex members. Mutations within MBD domains occur in many diseases, including neurological disorders and cancers, leading to loss of MBD binding specificity to methylated sites and gene deregulation. Here, we summarize the current state of knowledge about MBD proteins and their role as readers of the epigenome.
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“5mC readers including proteins containing a methyl-CpG-binding domain such as MECP2 or MBD proteins can recognize 5mC and recruit co-regulators to methylated DNA (25).”
From Dynamic DNA methylation: In the right place at the right time (2018) · cites this paper as [25]
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1 retracted
Sarraf, S. A., & Stancheva, I. (2004) · Molecular Cell · doi:10.1016/j.molcel.2004.06.043 · Cited by 501
RetractedCerami, E., Gao, J., Dogrusoz, U., Gross, B. E., Sumer, S. O., Aksoy, B. A., Jacobsen, A., Byrne, C. J., Heuer, M. L., Larsson, E., et al. (2012) · Cancer Discovery · doi:10.1158/2159-8290.cd-12-0095 · Cited by 17,455
Integrative Analysis of Complex Cancer Genomics and Clinical Profiles Using the cBioPortal
Gao, J., Aksoy, B. A., Dogrusoz, U., Dresdner, G., Gross, B., Sumer, S. O., Sun, Y., Jacobsen, A., Sinha, R., Larsson, E., et al. (2013) · Science Signaling · doi:10.1126/scisignal.2004088 · Cited by 15,160
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
Nan, X., Ng, H.-H., Johnson, C. A., Laherty, C. D., Turner, B. M., Eisenman, R. N., & Bird, A. (1998) · Nature · doi:10.1038/30764 · Cited by 3,440
CpG Islands in vertebrate genomes
Gardiner‐Garden, M., & Frommer, M. (1987) · Journal of Molecular Biology · doi:10.1016/0022-2836(87)90689-9 · Cited by 3,417
Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription
Jones, P. L., Veenstra, G. J. C., Wade, P. A., Vermaak, D., Kass, S. U., Landsberger, N., Strouboulis, J., & Wolffe, A. P. (1998) · Nature Genetics · doi:10.1038/561 · Cited by 2,791
Linking DNA methylation and histone modification: patterns and paradigms
Cedar, H., & Bergman, Y. (2009) · Nature Reviews Genetics · doi:10.1038/nrg2540 · Cited by 2,267
Cloning and characterization of a family of novel mammalian DNA (cytosine-5) methyltransferases
Okano, M., Xie, S., & Li, E. (1998) · Nature Genetics · doi:10.1038/890 · Cited by 1,643
Identification and Characterization of a Family of Mammalian Methyl-CpG Binding Proteins
Hendrich, B., & Bird, A. P. (1998) · Molecular and Cellular Biology · doi:10.1128/mcb.18.11.6538 · Cited by 1,386
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Pandey, S., Simmons, G. E., Jr., Malyarchuk, S., Calhoun, T. N., & Pruitt, K. (2015) · Genes & Cancer · doi:10.18632/genesandcancer.84 · Cited by 34
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Qiu, Y., Xu, Q., Xie, P., He, C., Li, Q., Yao, X., Mao, Y. H., Wu, X., & Zhang, T. (2024) · Pharmacological Research · doi:10.1016/j.phrs.2024.107546 · Cited by 33
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Brandt, B., Rashidiani, S., Bán, Á., & Rauch, T. A. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20225646 · Cited by 35
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Ong, L. T. C., Booth, D. R., & Parnell, G. P. (2020) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202000437 · Cited by 33
DNA methylation and histone variants in aging and cancer
Mangelinck, A., & Mann, C. (2021) · International review of cytology · doi:10.1016/bs.ircmb.2021.06.002 · Cited by 35
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 36
Uppala, S. N., Tryphena, K. P., Naren, P., Srivastava, S., Singh, S. B., & Khatri, D. K. (2023) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2023.111826 · Cited by 32
Buchmuller, B. C., Kosel, B., & Summerer, D. (2020) · Scientific Reports · doi:10.1038/s41598-020-61030-1 · Cited by 32
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Kumar, S., & Kim, Y. (2017) · Scientific Reports · doi:10.1038/srep43287 · Cited by 31
Myxosporea (Myxozoa, Cnidaria) Lack DNA Cytosine Methylation
Kyger, R., Luzuriaga-Neira, A., Layman, T. S., Sandberg, T. O. M., Singh, D., Huchon, D., Peri, S., Atkinson, S. D., Bartholomew, J. L., Yi, S. V., et al. (2020) · Molecular Biology and Evolution · doi:10.1093/molbev/msaa214 · Cited by 31
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Seethy, A. A., Pethusamy, K., Chattopadhyay, I., Sah, R., Chopra, A., Dhar, R., & Karmakar, S. (2021) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-021-03537-5 · Cited by 31
Lopez, M., Gilbert, J., Contreras, J., Halby, L., & Arimondo, P. B. (2022) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-11454-0_17 · Cited by 32
MBD2-mediated Th17 differentiation in severe asthma is associated with impaired SOCS3 expression
Sun, W., Xiao, B., Jia, A., Qiu, L., Zeng, Q., Liu, D., Yuan, Y. L., Jia, J., Zhang, X., & Xiang, X. (2018) · Experimental Cell Research · doi:10.1016/j.yexcr.2018.08.010 · Cited by 30
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Seo, K. W., & Kleiner, R. E. (2020) · Biopolymers · doi:10.1002/bip.23403 · Cited by 32
Batsché, É., Yi, J., Mauger, O., Kornobis, É., Hopkins, B., Hanmer-Lloyd, C., & Muchardt, C. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkab437 · Cited by 31
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Tian, M., Xia, P., Lu, Y., Gou, X., Giesy, J. P., Dai, J., Yu, H., & Zhang, X. (2022) · Environmental Science & Technology · doi:10.1021/acs.est.1c07945 · Cited by 30
Chen, L., Zhou, A. S., & West, A. E. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00067.2017 · Cited by 35
MTA1 expression in human cancers – Clinical and pharmacological significance
Malisetty, V. L., Penugurti, V., Panta, P., Chitta, S. K., & Manavathi, B. (2017) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2017.09.025 · Cited by 30
Dhat, R., Mongad, D., Raji, S., Arkat, S., Mahapatra, N. R., Singhal, N., & Sitasawad, S. L. (2023) · Epigenetics & Chromatin · doi:10.1186/s13072-023-00489-4 · Cited by 33
Epigenomics-Guided Drug Development: Recent Advances in Solving the Cancer Treatment “jigsaw puzzle”
Dzobo, K. (2019) · OMICS A Journal of Integrative Biology · doi:10.1089/omi.2018.0206 · Cited by 29
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Grimanelli, D., & Ingouff, M. (2020) · Journal of Molecular Biology · doi:10.1016/j.jmb.2019.12.043 · Cited by 31
Trnkova, L., Buociková, V., Mego, M., Čumová, A., Buríková, M., Boháč, M., Miklikova, S., Cihova, M., & Smolková, B. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116559 · Cited by 29
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Jin, Y., Liu, T., Luo, H., Liu, Y., & Liu, D. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.848221 · Cited by 28
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Turpin, M., & Salbert, G. (2022) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2022.976862 · Cited by 31
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Wu, W.-F., Lin, J.-T., Qiu, Y.-K., Dong, W., Wan, J., Li, S., Zheng, H., & Wu, Y.-Q. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.101983 · Cited by 28
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Jiang, P., Wang, H., Zheng, J., Han, Y., Huang, H., & Qian, P. (2019) · Blood Science · doi:10.1097/bs9.0000000000000018 · Cited by 29
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Dong, A., Yang, Y., Liu, S., Zenda, T., Liu, X., Wang, Y., Li, J., & Duan, H. (2020) · Biotechnology & Biotechnological Equipment · doi:10.1080/13102818.2020.1805015 · Cited by 27
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Stachecka, J., Lemanska, W., Noak, M., & Szczerbal, I. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.11.175 · Cited by 26
Methylation dynamics during folliculogenesis and early embryo development in sheep
Masala, L., Burrai, G. P., Bellu, E., Ariu, F., Bogliolo, L., Ledda, S., & Bebbere, D. (2017) · Reproduction · doi:10.1530/rep-16-0644 · Cited by 26
Awamleh, Z., Chater‐Diehl, E., Choufani, S., Wei, E. Y., Kianmahd, R. R., Yu, A., Chad, L., Costain, G., Tan, W., Scherer, S. W., et al. (2022) · European Journal of Human Genetics · doi:10.1038/s41431-022-01083-0 · Cited by 26
Structural analyses reveal that MBD 3 is a methylated CG binder
Liu, K., Lei, M., Wu, Z., Gan, B. S., Cheng, H., Li, Y., & Min, J. (2019) · FEBS Journal · doi:10.1111/febs.14850 · Cited by 26
Qu, M., Zhang, Z., Liang, T., Niu, P., Wu, M., Chi, W., Chen, Z., Chen, Z., Zhang, S., & Chen, S. (2021) · BMC Plant Biology · doi:10.1186/s12870-021-02880-3 · Cited by 25
Romanelli, M. N., Borgonetti, V., & Galeotti, N. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105901 · Cited by 25
Kouter, K., Zupanc, T., & Paska, A. V. (2022) · The World Journal of Biological Psychiatry · doi:10.1080/15622975.2022.2046291 · Cited by 26
Lagos, C., Carvajal, P., Castro, I., Jara, D., González, S., Aguilera, S., Barrera, M., Quest, A. F. G., Bahamondes, V., Molina, C., et al. (2018) · Clinical Immunology · doi:10.1016/j.clim.2018.06.002 · Cited by 25
MiR-520b inhibits the development of glioma by directly targeting MBD2.
Cui, S., Liu, L., Wan, T., Jiang, L., Shi, Y., & Luo, L. (2017) · PubMed Central · Cited by 25
Methyl-CpG binding domain 2 (Mbd2) is an epigenetic regulator of autism-risk genes and cognition
Lax, E., Carmo, S. D., Enuka, Y., Sapozhnikov, D. M., Welikovitch, L. A., Mahmood, N., Rabbani, S. A., Wang, L., Britt, J. P., Hancock, W. W., et al. (2023) · Translational Psychiatry · doi:10.1038/s41398-023-02561-9 · Cited by 25
Pathogenesis and biomarkers of colorectal cancer by epigenetic alteration
Oh, C. K., & Cho, Y. (2024) · Intestinal Research · doi:10.5217/ir.2023.00115 · Cited by 24
Geyer, K. K., Munshi, S. E., Whiteland, H., Fernández‐Fuentes, N., Phillips, D. W., & Hoffmann, K. F. (2018) · PLoS Pathogens · doi:10.1371/journal.ppat.1007107 · Cited by 23
Vaidergorn, M. D. M., Emery, F. D. S., & Ganesan, A. (2021) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.1c00787 · Cited by 23
Sui, J., Qiao, W., Xiang, X., & Luo, Y. (2022) · Pharmacological Research · doi:10.1016/j.phrs.2022.106195 · Cited by 24
Duan, W., Huang, J., Wasti, B., Chen, Z., Yuan, Y. L., He, Y., Li, D., Jia, J., Liu, S., Liu, Y., et al. (2023) · Clinical and Experimental Medicine · doi:10.1007/s10238-023-01033-0 · Cited by 23
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Ramesh, R. P. G., Yasmin, H., Ponnachan, P., al-Ramadi, B. K., Kishore, U., & Joseph, A. M. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1573522 · Cited by 22
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Coelho, A. A., Bastos, S., Gobira, P. H., & Lisboa, S. F. D. S. (2023) · Neuronal Signaling · doi:10.1042/ns20220034 · Cited by 22
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Maurer, S., Gieß, M., Koch, O., & Summerer, D. (2016) · ACS Chemical Biology · doi:10.1021/acschembio.6b00627 · Cited by 22
Kawarai, Y., Jang, S. H., Lee, S., Millecamps, M., Kang, H., Grégoire, S., Suzuki, M., Ohtori, S., & Stone, L. S. (2021) · The Spine Journal · doi:10.1016/j.spinee.2021.06.002 · Cited by 22
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Dietary Restriction and Epigenetics: Part I.
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Im, H., Song, Y., Jung, Y. H., Kim, J. K., Park, D., Kim, H., Kim, H., & Shin, J.-O. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26031382 · Cited by 20
Shi, R., Zhang, J., Li, J., Wang, K., Jia, H., Zhang, L., Wang, P., Yin, J., Meng, F., & Li, Y. (2016) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2016.08.024 · Cited by 19
Epigenomic alterations in cancer: mechanisms and therapeutic potential
Gray, J. S., Wani, S. A., & Campbell, M. J. (2022) · Clinical Science · doi:10.1042/cs20210449 · Cited by 19
Fritz, A. J., Dika, M. E., Toor, R. H., Rodriguez, P. D., Foley, S. J., Ullah, R., Nie, D., Banerjee, B., Lohese, D., Tracy, K. M., et al. (2022) · Results and problems in cell differentiation · doi:10.1007/978-3-031-06573-6_12 · Cited by 23
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Sarathy, A., Athreya, N. B. M., Varshney, L. R., & Leburton, J. (2018) · The Journal of Physical Chemistry Letters · doi:10.1021/acs.jpclett.8b02200 · Cited by 19
Weidner, M. T., Lardenoije, R., Eijssen, L., Mogavero, F., de Groodt, L., Popp, S., Palme, R., Förstner, K. U., Strekalova, T. V., Steinbusch, H. W. M., et al. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00460 · Cited by 19
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Wasti, B., Chen, Z., He, Y., Duan, W., Liu, S., & Xiang, X. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/7097797 · Cited by 18
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Hao, Y., Zhou, Z., Liu, R., Shen, S., Liu, H., Zhou, Y., Sun, Y., Mao, Q., Zhang, T., Li, S., et al. (2024) · Nature Chemical Biology · doi:10.1038/s41589-024-01776-1 · Cited by 18
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Zhou, M., Zhou, K., Cheng, L., Chen, X., Wang, J., Wang, X., Zhang, Y., Yu, Q., Zhang, S., Wang, D., et al. (2018) · Cancer Research · doi:10.1158/0008-5472.can-17-1434 · Cited by 18
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Hu, J., Ding, R., Liu, S., Wang, J., Li, J., & Shang, Y. (2023) · iScience · doi:10.1016/j.isci.2023.107503 · Cited by 17
Palei, S., Buchmuller, B. C., Wolffgramm, J., Muñoz‐López, Á., Jung, S., Czodrowski, P., & Summerer, D. (2020) · Journal of the American Chemical Society · doi:10.1021/jacs.0c01193 · Cited by 17
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Wu, Z., Chen, S., Zhou, M., Jia, L., Li, Z., Zhang, X., Min, J., & Liu, K. (2021) · Journal of Molecular Biology · doi:10.1016/j.jmb.2021.167404 · Cited by 17
Zhang, Y., Yang, Y., Zhang, F.-L., Liao, X.-H., Shao, Z., & Li, D. (2018) · Cancer Medicine · doi:10.1002/cam4.1324 · Cited by 17
5-Hydroxymethylcytosine: a key epigenetic mark in cancer and chemotherapy response
Kharat, S. S., & Sharan, S. K. (2025) · Epigenetics & Chromatin · doi:10.1186/s13072-025-00636-z · Cited by 16
Ghosh, K. K., Chatterjee, B., Nalla, K., Behera, B., Mukherjee, A. K., & Kanade, S. R. (2022) · Chemosphere · doi:10.1016/j.chemosphere.2022.133569 · Cited by 17
Wang, S., Dong, J., Zhao, X., Song, X., Long, Y., & Xing, Z. (2023) · BMC Genomics · doi:10.1186/s12864-023-09191-x · Cited by 16
Hashimoto, J. G., Gavin, D. P., Wiren, K. M., Crabbe, J. C., & Guizzetti, M. (2017) · Alcohol · doi:10.1016/j.alcohol.2017.01.010 · Cited by 17
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Metadata
- Authors
- Du, Q., Luu, P.-L., Stirzaker, C., & Clark, S. J.
- Affiliations
- Garvan Institute of Medical Research (AU)
- Venue
- Epigenomics
- Publisher
- Informa UK Limited
- Published
- 2015-04-30
- Volume
- 7
- Issue
- 6
- Pages
- 1051-1073
- ISSN
- 1750-1911 (ISSN-L)
- 1750-192X
- OpenAlex
- W2040875973
- Cited by
- 544
- References
- 191
- Citations by year
- 2026: 34 · 2025: 61 · 2024: 55 · 2023: 53 · 2022: 74 · 2021: 72 · 2020: 43 · 2019: 47 · 2018: 34 · 2017: 35 · 2016: 23 · 2015: 5
- FWCI
- 3.13
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Epigenomics (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Funders
- NHMRC Fellowship and NHMRC (1088144)
- Stirzaker and P-L Luu by NHMRC (1088144)
- 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 › Cancer-related gene regulation
- Keywords
- methyl-CpG binding domain proteins, DNA methylation, epigenetic reader protein, chromatin remodeling, histone deacetylase, gene repression, neurological disorders, cancer, gene expression regulation
- MeSH terms
- Animals, Binding Sites, Cell Differentiation, DNA-Binding Proteins, Gene Expression Regulation, Multigene Family, Humans, Mutation, Neoplasms, Protein Binding, Down-Regulation, CpG Islands, DNA Methylation, Genetic Predisposition to Disease, Gene Silencing, Epigenesis, Genetic, Protein Interaction Domains and Motifs, Cellular Reprogramming
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