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Epigenetic reprogramming in mouse pre-implantation development and primordial germ cells
Abstract
Epigenetic modifications are crucial for the identity and stability of cells, and, when aberrant, can lead to disease. During mouse development, the genome-wide epigenetic states of pre-implantation embryos and primordial germ cells (PGCs) undergo extensive reprogramming. An improved understanding of the epigenetic reprogramming mechanisms that occur in these cells should provide important new information about the regulation of the epigenetic state of a cell and the mechanisms of induced pluripotency. Here, we discuss recent findings about the potential mechanisms of epigenetic reprogramming, particularly genome-wide DNA demethylation, in pre-implantation mouse embryos and PGCs.
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Cites
Initial sequencing and analysis of the human genome
International Human Genome Sequencing Consortium, Whitehead Institute for Biomedical Research, C. F. G. R., Lander, E. S., Linton, L. M., Birren, B., Nusbaum, C., Zody, M. C., Baldwin, J., Devon, K., Dewar, K., et al. (2001) · Nature · doi:10.1038/35057062 · Cited by 24,216
Initial sequencing and comparative analysis of the mouse genome
Mouse Genome Sequencing Consortium (2002) · Nature · doi:10.1038/nature01262 · Cited by 7,187
High-Resolution Profiling of Histone Methylations in the Human Genome
Barski, A., Cuddapah, S., Cui, K., Roh, T.-Y., Schones, D. E., Wang, Z., Wei, G., Chepelev, I., & Zhao, K. (2007) · Cell · doi:10.1016/j.cell.2007.05.009 · Cited by 6,845
Okano, M., Bell, D. W., Haber, D. A., & Li, E. (1999) · Cell · doi:10.1016/s0092-8674(00)81656-6 · Cited by 6,143
Conversion of 5-Methylcytosine to 5-Hydroxymethylcytosine in Mammalian DNA by MLL Partner TET1
Tahiliani, M., Koh, K. P., Shen, Y., Pastor, W. A., Bandukwala, H., Brudno, Y., Agarwal, S., Iyer, L. M., Liu, D. R., Aravind, L., et al. (2009) · Science · doi:10.1126/science.1170116 · Cited by 5,836
A bivalent chromatin structure marks key developmental genes in embryonic stem cells
Bernstein, B. E., Mikkelsen, T. S., Xie, X., Kamal, M., Huebert, D. J., Cuff, J., Fry, B., Meissner, A., Wernig, M., Plath, K., et al. (2006) · Cell · doi:10.1016/j.cell.2006.02.041 · Cited by 5,361
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
Genome-wide maps of chromatin state in pluripotent and lineage-committed cells
Mikkelsen, T. S., Ku, M., Jaffe, D. B., Issac, B., Lieberman, E., Giannoukos, G., Alvarez, P., Brockman, W., Kim, T.-K., Koche, R. P., et al. (2007) · Nature · doi:10.1038/nature06008 · Cited by 4,129
Targeted mutation of the DNA methyltransferase gene results in embryonic lethality
Li, E., Bestor, T. H., & Jaenisch, R. (1992) · Cell · doi:10.1016/0092-8674(92)90611-f · Cited by 3,984
Muramatsu, M., Kinoshita, K., Fagarasan, S., Yamada, S., Shinkai, Y., & Honjo, T. (2000) · Cell · doi:10.1016/s0092-8674(00)00078-7 · Cited by 3,474
Tet proteins can convert 5-methylcytosine to 5-formylcytosine and 5-carboxylcytosine
Ito, S., Shen, L., Dai, Q., Wu, S. C., Collins, L. B., Swenberg, J. A., He, C., & Zhang, Y. (2011) · Science · doi:10.1126/science.1210597 · Cited by 3,451
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
Epigenetic Reprogramming in Mammalian Development
Reik, W., Dean, W., & Walter, J. (2001) · Science · doi:10.1126/science.1063443 · Cited by 3,078
DNA methylation landscapes: Provocative insights from epigenomics
Suzuki, M. M., & Bird, A. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2341 · Cited by 3,039
Bird, A. (2007) · Nature · doi:10.1038/nature05913 · Cited by 3,011
Tet-Mediated Formation of 5-Carboxylcytosine and Its Excision by TDG in Mammalian DNA
He, Y.-F., Li, B.-Z., Li, Z., Liu, P., Wang, Y., Tang, Q., Ding, J., Jia, Y., Chen, Z., Li, L., et al. (2011) · Science · doi:10.1126/science.1210944 · Cited by 2,770
Figueroa, M. E., Abdel-Wahab, O., Lu, C., Ward, P. S., Patel, J., Shih, A., Li, Y., Bhagwat, N., Vasanthakumar, A., Fernandez, H. F., et al. (2010) · Cancer Cell · doi:10.1016/j.ccr.2010.11.015 · Cited by 2,766
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 2,730
The Nuclear DNA Base 5-Hydroxymethylcytosine Is Present in Purkinje Neurons and the Brain
Kriaucionis, S., & Heintz, N. (2009) · Science · doi:10.1126/science.1169786 · Cited by 2,700
Highly Integrated Single-Base Resolution Maps of the Epigenome in Arabidopsis
Lister, R., O'Malley, R. C., Tonti-Filippini, J., Gregory, B. D., Berry, C. C., Millar, A. H., & Ecker, J. R. (2008) · Cell · doi:10.1016/j.cell.2008.03.029 · Cited by 2,418
Ito, S., D’Alessio, A. C., Taranova, O. V., Hong, K., Sowers, L. C., & Zhang, Y. (2010) · Nature · doi:10.1038/nature09303 · Cited by 2,373
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 · cited 1×
“5mC and histone modifications 5mC and histone modifications act in concert to form an appropriate epigenome during development and in adult cells (Cedar and Bergman, 2009).”
BackgroundShotgun bisulphite sequencing of the Arabidopsis genome reveals DNA methylation patterning
Cokus, S. J., Feng, S., Zhang, X., Chen, Z., Merriman, B., Haudenschild, C. D., Pradhan, S., Nelson, S. F., Pellegrini, M., & Jacobsen, S. E. (2008) · Nature · doi:10.1038/nature06745 · Cited by 2,256
Weber, M., Hellmann, I., Stadler, M. B., Ramos, L., Pääbo, S., Rebhan, M., & Schübeler, D. (2007) · Nature Genetics · doi:10.1038/ng1990 · Cited by 2,221
The Polycomb group protein EZH2 directly controls DNA methylation
Viré, E., Brenner, C., Deplus, R., Blanchon, L., Fraga, M., Didelot, C., Morey, L., Van Eynde, A., Bernard, D., Vanderwinden, J.-M., et al. (2006) · Nature · doi:10.1038/nature04431 · Cited by 2,204
Bernstein, B. E., Meissner, A., & Lander, E. S. (2007) · Cell · doi:10.1016/j.cell.2007.01.033 · Cited by 2,086
A Chromatin Landmark and Transcription Initiation at Most Promoters in Human Cells
Guenther, M. G., Levine, S. S., Boyer, L. A., Jaenisch, R., & Young, R. A. (2007) · Cell · doi:10.1016/j.cell.2007.05.042 · Cited by 1,944
Weber, M., Davies, J. J., Wittig, D., Oakeley, E. J., Haase, M., Lam, W. L., & Schübeler, D. (2005) · Nature Genetics · doi:10.1038/ng1598 · Cited by 1,754
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 1,651
Revy, P., Muto, T., Levy, Y., Geissmann, F., Plebani, A., Sanal, O., Catalan, N., Forveille, M., Dufourcq-Lagelouse, R., Gennery, A., et al. (2000) · Cell · doi:10.1016/s0092-8674(00)00079-9 · Cited by 1,647
DNMT3L 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.-P., Allis, C. D., et al. (2007) · Nature · doi:10.1038/nature05987 · Cited by 1,567
UHRF1 Plays a Role in Maintaining DNA Methylation in Mammalian Cells
Bostick, M., Kim, J. K., Estève, P.-O., Clark, A., Pradhan, S., & Jacobsen, S. E. (2007) · Science · doi:10.1126/science.1147939 · Cited by 1,455
Dnmt3L and the Establishment of Maternal Genomic Imprints
Bourc'his, D., Xu, G.-L., Lin, C.-S., Bollman, B., & Bestor, T. H. (2001) · Science · doi:10.1126/science.1065848 · Cited by 1,439
Saxonov, S., Berg, P., & Brutlag, D. L. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0510310103 · Cited by 1,401
Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting
Kaneda, M., Okano, M., Hata, K., Sado, T., Tsujimoto, N., Li, E., & Sasaki, H. (2004) · Nature · doi:10.1038/nature02633 · Cited by 1,387
Reconstitution of the Mouse Germ Cell Specification Pathway in Culture by Pluripotent Stem Cells
Hayashi, K., Ohta, H., Kurimoto, K., Aramaki, S., & Saitou, M. (2011) · Cell · doi:10.1016/j.cell.2011.06.052 · Cited by 1,379
Self-citationHydroxylation of 5-Methylcytosine by TET1 Promotes Active DNA Demethylation in the Adult Brain
Guo, J. U., Su, Y., Zhong, C., Ming, G.-L., & Song, H. (2011) · Cell · doi:10.1016/j.cell.2011.03.022 · Cited by 1,360
Tet2 loss leads to increased hematopoietic stem cell self-renewal and myeloid transformation
Moran-Crusio, K., Reavie, L., Shih, A., Abdel-Wahab, O., Ndiaye-Lobry, D., Lobry, C., Figueroa, M. E., Vasanthakumar, A., Patel, J., Zhao, X., et al. (2011) · Cancer Cell · doi:10.1016/j.ccr.2011.06.001 · Cited by 1,339
Demethylation of the zygotic paternal genome
Mayer, W., Niveleau, A., Walter, J., Fundele, R., & Haaf, T. (2000) · Nature · doi:10.1038/35000656 · Cited by 1,327
Bmp4 is required for the generation of primordial germ cells in the mouse embryo
Lawson, K. A., Dunn, N. R., Roelen, B. A. J., Zeinstra, L. M., Davis, A. M., Wright, C. V. E., Korving, J. P. W. F. M., & Hogan, B. L. M. (1999) · Genes & Development · doi:10.1101/gad.13.4.424 · Cited by 1,310
The SRA protein Np95 mediates epigenetic inheritance by recruiting Dnmt1 to methylated DNA
Sharif, J., Muto, M., Takebayashi, S.-I., Suetake, I., Iwamatsu, A., Endo, T. A., Shinga, J., Mizutani-Koseki, Y., Toyoda, T., Okamura, K., et al. (2007) · Nature · doi:10.1038/nature06397 · Cited by 1,304
Tachibana, M., Sugimoto, K., Nozaki, M., Ueda, J., Ohta, T., Ohki, M., Fukuda, M., Takeda, N., Niida, H., Kato, H., et al. (2002) · Genes & Development · doi:10.1101/gad.989402 · Cited by 1,253
Lehnertz, B., Ueda, Y., Derijck, A. A. H. A., Braunschweig, U., Perez-Burgos, L., Kubicek, S., Chen, T., Li, E., Jenuwein, T., & Peters, A. H. F. M. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00432-9 · Cited by 1,245
Reduced representation bisulfite sequencing for comparative high-resolution DNA methylation analysis
Meissner, A. (2005) · Nucleic Acids Research · doi:10.1093/nar/gki901 · Cited by 1,217
Impaired hydroxylation of 5-methylcytosine in myeloid cancers with mutant TET2
Ko, M., Huang, Y., Jankowska, A. M., Pape, U. J., Tahiliani, M., Bandukwala, H. S., An, J., Lamperti, E. D., Koh, K. P., Ganetzky, R., et al. (2010) · Nature · doi:10.1038/nature09586 · Cited by 1,213
Dynamic Reprogramming of DNA Methylation in the Early Mouse Embryo
Santos, F., Hendrich, B., Reik, W., & Dean, W. (2002) · Developmental Biology · doi:10.1006/dbio.2001.0501 · Cited by 1,212
Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L
Bourc'his, D., & Bestor, T. H. (2004) · Nature · doi:10.1038/nature02886 · Cited by 1,207
Epigenetic reprogramming in mouse primordial germ cells
Hajkova, P., Erhardt, S., Lane, N., Haaf, T., El-Maarri, O., Reik, W., Walter, J., & Surani, M. A. (2002) · Mechanisms of Development · doi:10.1016/s0925-4773(02)00181-8 · Cited by 1,191
Methylation of tRNA Asp by the DNA Methyltransferase Homolog Dnmt2
Goll, M. G., Kirpekar, F., Maggert, K. A., Yoder, J. A., Hsieh, C.-L., Zhang, X., Golic, K. G., Jacobsen, S. E., & Bestor, T. H. (2006) · Science · doi:10.1126/science.1120976 · Cited by 1,190
Muramatsu, M., Sankaranand, V. S., Anant, S., Sugai, M., Kinoshita, K., Davidson, N. O., & Honjo, T. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.26.18470 · Cited by 1,176
The role of Tet3 DNA dioxygenase in epigenetic reprogramming by oocytes
Gu, T.-P., Guo, F., Yang, H., Wu, H.-P., Xu, G.-F., Liu, W., Xie, Z.-G., Shi, L., He, X., Jin, S.-G., et al. (2011) · Nature · doi:10.1038/nature10443 · Cited by 1,139
Dynamic regulation of 5-hydroxymethylcytosine in mouse ES cells and during differentiation
Ficz, G., Branco, M. R., Seisenberger, S., Santos, F., Krueger, F., Hore, T. A., Marques, C. J., Andrews, S., & Reik, W. (2011) · Nature · doi:10.1038/nature10008 · Cited by 1,133
Molecular Mechanisms of Antibody Somatic Hypermutation
Di Noia, J. M., & Neuberger, M. S. (2007) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.76.061705.090740 · Cited by 1,106
Monk, M., Boubelik, M., & Lehnert, S. (1987) · Development · doi:10.1242/dev.99.3.371 · Cited by 1,094
Role of transposable elements in heterochromatin and epigenetic control
Lippman, Z., Gendrel, A.-V., Black, M., Vaughn, M. W., Dedhia, N., Richard McCombie, W., Lavine, K., Mittal, V., May, B., Kasschau, K. D., et al. (2004) · Nature · doi:10.1038/nature02651 · Cited by 1,065
Blimp1 is a critical determinant of the germ cell lineage in mice
Ohinata, Y., Payer, B., O'Carroll, D., Ancelin, K., Ono, Y., Sano, M., Barton, S. C., Obukhanych, T., Nussenzweig, M., Tarakhovsky, A., et al. (2005) · Nature · doi:10.1038/nature03813 · Cited by 1,046
Self-citationHata, K., Okano, M., Lei, H., & Li, E. (2002) · Development · doi:10.1242/dev.129.8.1983 · Cited by 1,039
TET1 and hydroxymethylcytosine in transcription and DNA methylation fidelity
Williams, K., Christensen, J., Pedersen, M. T., Johansen, J. V., Cloos, P. A. C., Rappsilber, J., & Helin, K. (2011) · Nature · doi:10.1038/nature10066 · Cited by 1,021
Primordial germ cells in the mouse embryo during gastrulation
Ginsburg, M., Snow, M. H. L., & McLaren, A. (1990) · Development · doi:10.1242/dev.110.2.521 · Cited by 1,004
Active demethylation of the paternal genome in the mouse zygote
Oswald, J., Engemann, S., Lane, N., Mayer, W., Olek, A., Fundele, R., Dean, W., Reik, W., & Walter, J. (2000) · Current Biology · doi:10.1016/s0960-9822(00)00448-6 · Cited by 981
Ramsahoye, B. H., Biniszkiewicz, D., Lyko, F., Clark, V., Bird, A. P., & Jaenisch, R. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.10.5237 · Cited by 970
Quivoron, C., Couronné, L., Della Valle, V., Lopez, C. K., Plo, I., Wagner-Ballon, O., Do Cruzeiro, M., Delhommeau, F., Arnulf, B., Stern, M.-H., et al. (2011) · Cancer Cell · doi:10.1016/j.ccr.2011.06.003 · Cited by 924
Neuronal Activity–Induced Gadd45b Promotes Epigenetic DNA Demethylation and Adult Neurogenesis
Ma, D. K., Jang, M.-H., Guo, J. U., Kitabatake, Y., Chang, M.-L., Pow-anpongkul, N., Flavell, R. A., Lu, B., Ming, G.-L., & Song, H. (2009) · Science · doi:10.1126/science.1166859 · Cited by 924
Mohn, F., Weber, M., Rebhan, M., Roloff, T. C., Richter, J., Stadler, M. B., Bibel, M., & Schübeler, D. (2008) · Molecular Cell · doi:10.1016/j.molcel.2008.05.007 · Cited by 917
Cloning and sequencing of a cDNA encoding DNA methyltransferase of mouse cells
Bestor, T., Laudano, A., Mattaliano, R., & Ingram, V. (1988) · Journal of Molecular Biology · doi:10.1016/0022-2836(88)90122-2 · Cited by 913
Molecular Signals of Epigenetic States
Bonasio, R., Tu, S., & Reinberg, D. (2010) · Science · doi:10.1126/science.1191078 · Cited by 912
A molecular programme for the specification of germ cell fate in mice
Saitou, M., Barton, S. C., & Surani, M. A. (2002) · Nature · doi:10.1038/nature00927 · Cited by 893
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., Jacobsen, S. E., & Reik, W. (2010) · Nature · doi:10.1038/nature08829 · Cited by 860
Tachibana, M., Ueda, J., Fukuda, M., Takeda, N., Ohta, T., Iwanari, H., Sakihama, T., Kodama, T., Hamakubo, T., & Shinkai, Y. (2005) · Genes & Development · doi:10.1101/gad.1284005 · Cited by 845
De novo DNA cytosine methyltransferase activities in mouse embryonic stem cells
Lei, H., Oh, S. P., Okano, M., Jüttermann, R., Goss, K. A., Jaenisch, R., & Li, E. (1996) · Development · doi:10.1242/dev.122.10.3195 · Cited by 816
Cortellino, S., Xu, J., Sannai, M., Moore, R., Caretti, E., Cigliano, A., Le Coz, M., Devarajan, K., Wessels, A., Soprano, D., et al. (2011) · Cell · doi:10.1016/j.cell.2011.06.020 · Cited by 809
Genome-wide mapping of 5-hydroxymethylcytosine in embryonic stem cells
Pastor, W. A., Pape, U. J., Huang, Y., Henderson, H. R., Lister, R., Ko, M., McLoughlin, E. M., Brudno, Y., Mahapatra, S., Kapranov, P., et al. (2011) · Nature · doi:10.1038/nature10102 · Cited by 804
Mutagenic deamination of cytosine residues in DNA
Duncan, B. K., & Miller, J. H. (1980) · Nature · doi:10.1038/287560a0 · Cited by 792
5-Hydroxymethylcytosine in the mammalian zygote is linked with epigenetic reprogramming
Wossidlo, M., Nakamura, T., Lepikhov, K., Marques, C. J., Zakhartchenko, V., Boiani, M., Arand, J., Nakano, T., Reik, W., & Walter, J. (2011) · Nature Communications · doi:10.1038/ncomms1240 · Cited by 792
Nuclear reprogramming to a pluripotent state by three approaches
Yamanaka, S., & Blau, H. M. (2010) · Nature · doi:10.1038/nature09229 · Cited by 776
Koh, K. P., Yabuuchi, A., Rao, S., Huang, Y., Cunniff, K., Nardone, J., Laiho, A., Tahiliani, M., Sommer, C. A., Mostoslavsky, G., et al. (2011) · Cell Stem Cell · doi:10.1016/j.stem.2011.01.008 · Cited by 776
The DNA methyltransferases associate with HP1 and the SUV39H1 histone methyltransferase
Fuks, F. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg332 · Cited by 760
Gadd45a promotes epigenetic gene activation by repair-mediated DNA demethylation
Barreto, G., Schäfer, A., Marhold, J., Stach, D., Swaminathan, S. K., Handa, V., Döderlein, G., Maltry, N., Wu, W., Lyko, F., et al. (2007) · Nature · doi:10.1038/nature05515 · Cited by 758
Valinluck, V. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh739 · Cited by 756
Chen, T., Ueda, Y., Dodge, J. E., Wang, Z., & Li, E. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.16.5594-5605.2003 · Cited by 751
Active DNA Demethylation Mediated by DNA Glycosylases
Zhu, J.-K. (2009) · Annual Review of Genetics · doi:10.1146/annurev-genet-102108-134205 · Cited by 745
Developmental pattern of gene-specific DNA methylation in the mouse embryo and germ line.
Kafri, T., Ariel, M., Brandeis, M., Shemer, R., Urven, L., McCarrey, J., Cedar, H., & Razin, A. (1992) · Genes & Development · doi:10.1101/gad.6.5.705 · Cited by 736
Whole-Genome Analysis of Histone H3 Lysine 4 and Lysine 27 Methylation in Human Embryonic Stem Cells
Pan, G., Tian, S., Nie, J., Yang, C., Ruotti, V., Wei, H., Jonsdottir, G. A., Stewart, R., & Thomson, J. A. (2007) · Cell Stem Cell · doi:10.1016/j.stem.2007.08.003 · Cited by 711
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. R., & Kelsey, G. (2011) · Nature Genetics · doi:10.1038/ng.864 · Cited by 699
Pluripotency and Cellular Reprogramming: Facts, Hypotheses, Unresolved Issues
Hanna, J. H., Saha, K., & Jaenisch, R. (2010) · Cell · doi:10.1016/j.cell.2010.10.008 · Cited by 698
Iqbal, K., Jin, S.-G., Pfeifer, G. P., & Szabó, P. E. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1014033108 · Cited by 692
Bransteitter, R., Pham, P., Scharff, M. D., & Goodman, M. F. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0730835100 · Cited by 680
Acquired mutations in TET2 are common in myelodysplastic syndromes
Langemeijer, S. M. C., Kuiper, R. P., Berends, M., Knops, R., Aslanyan, M. G., Massop, M., Stevens-Linders, E., van Hoogen, P., van Kessel, A. G., Raymakers, R. A. P., et al. (2009) · Nature Genetics · doi:10.1038/ng.391 · Cited by 680
Reprogramming towards pluripotency requires AID-dependent DNA demethylation
Bhutani, N., Brady, J. J., Damian, M., Sacco, A., Corbel, S. Y., & Blau, H. M. (2010) · Nature · doi:10.1038/nature08752 · Cited by 676
Lane, N., Dean, W., Erhardt, S., Hajkova, P., Surani, A., Walter, J., & Reik, W. (2003) · genesis · doi:10.1002/gene.10168 · Cited by 667
Chromatin dynamics during epigenetic reprogramming in the mouse germ line
Hajkova, P., Ancelin, K., Waldmann, T., Lacoste, N., Lange, U. C., Cesari, F., Lee, C., Almouzni, G., Schneider, R., & Surani, M. A. (2008) · Nature · doi:10.1038/nature06714 · Cited by 664
Genetic and Epigenetic Regulators of Pluripotency
Surani, M. A., Hayashi, K., & Hajkova, P. (2007) · Cell · doi:10.1016/j.cell.2007.02.010 · Cited by 658
DNA Demethylation in Zebrafish Involves the Coupling of a Deaminase, a Glycosylase, and Gadd45
Rai, K., Huggins, I. J., James, S. R., Karpf, A. R., Jones, D. A., & Cairns, B. R. (2008) · Cell · doi:10.1016/j.cell.2008.11.042 · Cited by 657
Genome-Wide Demethylation of Arabidopsis Endosperm
Hsieh, T.-F., Ibarra, C. A., Silva, P., Zemach, A., Eshed-Williams, L., Fischer, R. L., & Zilberman, D. (2009) · Science · doi:10.1126/science.1172417 · Cited by 650
A Bayesian deconvolution strategy for immunoprecipitation-based DNA methylome analysis
Down, T. A., Rakyan, V. K., Turner, D. J., Flicek, P., Li, H., Kulesha, E., Gräf, S., Johnson, N., Herrero, J., Tomazou, E. M., et al. (2008) · Nature Biotechnology · doi:10.1038/nbt1414 · Cited by 648
Dual functions of Tet1 in transcriptional regulation in mouse embryonic stem cells
Wu, H., D’Alessio, A. C., Ito, S., Xia, K., Wang, Z., Cui, K., Zhao, K., Eve Sun, Y., & Zhang, Y. (2011) · Nature · doi:10.1038/nature09934 · Cited by 646
Xu, Y., Wu, F., Tan, L., Kong, L., Xiong, L., Deng, J., Barbera, A. J., Zheng, L., Zhang, H., Huang, S., et al. (2011) · Molecular Cell · doi:10.1016/j.molcel.2011.04.005 · Cited by 632
Blastocyst lineage formation, early embryonic asymmetries and axis patterning in the mouse
Rossant, J., & Tam, P. P. L. (2009) · Development · doi:10.1242/dev.017178 · Cited by 631
CpG islands influence chromatin structure via the CpG-binding protein Cfp1
Thomson, J. P., Skene, P. J., Selfridge, J., Clouaire, T., Guy, J., Webb, S., Kerr, A. R. W., Deaton, A., Andrews, R., James, K. D., et al. (2010) · Nature · doi:10.1038/nature08924 · Cited by 625
Zhao, X. D., Han, X., Chew, J. L., Liu, J., Chiu, K. P., Choo, A., Orlov, Y. L., Sung, W.-K., Shahab, A., Kuznetsov, V. A., et al. (2007) · Cell Stem Cell · doi:10.1016/j.stem.2007.08.004 · Cited by 615
Wyatt, G. R., & Cohen, S. S. (1953) · Biochemical Journal · doi:10.1042/bj0550774 · Cited by 608
Targets and dynamics of promoter DNA methylation during early mouse development
Borgel, J., Guibert, S., Li, Y., Chiba, H., Schübeler, D., Sasaki, H., Forné, T., & Weber, M. (2010) · Nature Genetics · doi:10.1038/ng.708 · Cited by 601
Critical function of Prdm14 for the establishment of the germ cell lineage in mice
Yamaji, M., Seki, Y., Kurimoto, K., Yabuta, Y., Yuasa, M., Shigeta, M., Yamanaka, K., Ohinata, Y., & Saitou, M. (2008) · Nature Genetics · doi:10.1038/ng.186 · Cited by 581
Self-citationPGC7/Stella protects against DNA demethylation in early embryogenesis
Nakamura, T., Arai, Y., Umehara, H., Masuhara, M., Kimura, T., Taniguchi, H., Sekimoto, T., Ikawa, M., Yoneda, Y., Okabe, M., et al. (2007) · Nature Cell Biology · doi:10.1038/ncb1519 · Cited by 580
Extensive Demethylation of Repetitive Elements During Seed Development Underlies Gene Imprinting
Gehring, M., Bubb, K. L., & Henikoff, S. (2009) · Science · doi:10.1126/science.1171609 · Cited by 571
Cooperativity between DNA Methyltransferases in the Maintenance Methylation of Repetitive Elements
Liang, G., Chan, M. F., Tomigahara, Y., Tsai, Y. C., Gonzales, F. A., Li, E., Laird, P. W., & Jones, P. A. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.2.480-491.2002 · Cited by 569
A Signaling Principle for the Specification of the Germ Cell Lineage in Mice
Ohinata, Y., Ohta, H., Shigeta, M., Yamanaka, K., Wakayama, T., & Saitou, M. (2009) · Cell · doi:10.1016/j.cell.2009.03.014 · Cited by 555
Self-citationProliferation and migration of primordial germ cells during compensatory growth in mouse embryos
Tam, P. P. L., & Snow, M. H. L. (1981) · Development · doi:10.1242/dev.64.1.133 · Cited by 550
The AID/APOBEC family of nucleic acid mutators
Conticello, S. G. (2008) · Genome Biology · doi:10.1186/gb-2008-9-6-229 · Cited by 546
Seki, Y., Hayashi, K., Itoh, K., Mizugaki, M., Saitou, M., & Matsui, Y. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2004.11.025 · Cited by 544
Self-citationTsumura, A., Hayakawa, T., Kumaki, Y., Takebayashi, S., Sakaue, M., Matsuoka, C., Shimotohno, K., Ishikawa, F., Li, E., Ueda, H. R., et al. (2006) · Genes to Cells · doi:10.1111/j.1365-2443.2006.00984.x · Cited by 542
Molecular Cloning of an Apolipoprotein B Messenger RNA Editing Protein
Teng, B., Burant, C. F., & Davidson, N. O. (1993) · Science · doi:10.1126/science.8511591 · Cited by 536
Direct interaction between DNMT1 and G9a coordinates DNA and histone methylation during replication
Estève, P.-O., Chin, H. G., Smallwood, A., Feehery, G. R., Gangisetty, O., Karpf, A. R., Carey, M. F., & Pradhan, S. (2006) · Genes & Development · doi:10.1101/gad.1463706 · Cited by 536
X Chromosome Dosage Compensation: How Mammals Keep the Balance
Payer, B., & Lee, J. T. (2008) · Annual Review of Genetics · doi:10.1146/annurev.genet.42.110807.091711 · Cited by 521
Dawlaty, M. M., Ganz, K., Powell, B. E., Hu, Y.-C., Markoulaki, S., Cheng, A. W., Gao, Q., Kim, J., Choi, S.-W., Page, D. C., et al. (2011) · Cell stem cell · doi:10.1016/j.stem.2011.07.010 · Cited by 508
Valinluck, V., & Sowers, L. C. (2007) · Cancer Research · doi:10.1158/0008-5472.can-06-3123 · Cited by 501
Morgan, H. D., Dean, W., Coker, H. A., Reik, W., & Petersen-Mahrt, S. K. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m407695200 · Cited by 493
Hirasawa, R., Chiba, H., Kaneda, M., Tajima, S., Li, E., Jaenisch, R., & Sasaki, H. (2008) · Genes & Development · doi:10.1101/gad.1667008 · Cited by 489
The Discovery of 5‐Formylcytosine in Embryonic Stem Cell DNA
Pfaffeneder, T., Hackner, B., Truß, M., Münzel, M., Müller, M., Deiml, C. A., Hagemeier, C., & Carell, T. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201103899 · Cited by 483
Maternal control of early mouse development
Li, L., Zheng, P., & Dean, J. (2010) · Development · doi:10.1242/dev.039487 · Cited by 481
Epigenetic dynamics of stem cells and cell lineage commitment: digging Waddington's canal
Hemberger, M., Dean, W., & Reik, W. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2727 · Cited by 476
Genome-Wide Reprogramming in the Mouse Germ Line Entails the Base Excision Repair Pathway
Hajkova, P., Jeffries, S. J., Lee, C., Miller, N., Jackson, S. P., & Surani, M. A. (2010) · Science · doi:10.1126/science.1187945 · Cited by 473
Activation of mammalian DNA methyltransferase by cleavage of a Zn binding regulatory domain.
Bestor, T. H. (1992) · The EMBO Journal · doi:10.1002/j.1460-2075.1992.tb05326.x · Cited by 461
Seki, Y., Yamaji, M., Yabuta, Y., Sano, M., Shigeta, M., Matsui, Y., Saga, Y., Tachibana, M., Shinkai, Y., & Saitou, M. (2007) · Development · doi:10.1242/dev.005611 · Cited by 460
Self-citationComprehensive high-throughput arrays for relative methylation (CHARM)
Irizarry, R. A., Ladd-Acosta, C., Carvalho, B., Wu, H., Brandenburg, S. A., Jeddeloh, J. A., Wen, B., & Feinberg, A. P. (2008) · Genome Research · doi:10.1101/gr.7301508 · Cited by 433
Sensitive enzymatic quantification of 5-hydroxymethylcytosine in genomic DNA
Szwagierczak, A., Bultmann, S., Schmidt, C. S., Spada, F., & Leonhardt, H. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq684 · Cited by 432
G9a/GLP complexes independently mediate H3K9 and DNA methylation to silence transcription
Tachibana, M., Matsumura, Y., Fukuda, M., Kimura, H., & Shinkai, Y. (2008) · The EMBO Journal · doi:10.1038/emboj.2008.192 · Cited by 429
Chromosome methylation patterns during mammalian preimplantation development
Rougier, N., Bourc’his, D., Gomes, D. M., Niveleau, A., Plachot, M., Pàldi, A., & Viegas-Péquignot, E. (1998) · Genes & Development · doi:10.1101/gad.12.14.2108 · Cited by 428
Adenot, P. G., Mercier, Y., Renard, J.-P., & Thompson, E. M. (1997) · Development · doi:10.1242/dev.124.22.4615 · Cited by 427
Dnmt2 is not required for de novo and maintenance methylation of viral DNA in embryonic stem cells
Okano, M. (1998) · Nucleic Acids Research · doi:10.1093/nar/26.11.2536 · Cited by 423
Lee, J., Inoue, K., Ono, R., Ogonuki, N., Kohda, T., Kaneko-Ishino, T., Ogura, A., & Ishino, F. (2002) · Development · doi:10.1242/dev.129.8.1807 · Cited by 420
Epigenetic reprogramming during early development in mammals
Santos, F., & Dean, W. (2004) · Reproduction · doi:10.1530/rep.1.00221 · Cited by 411
Large-scale structure of genomic methylation patterns
Rollins, R. A., Haghighi, F., Edwards, J. R., Das, R., Zhang, M. Q., Ju, J., & Bestor, T. H. (2006) · Genome Research · doi:10.1101/gr.4362006 · Cited by 389
Embryonic lethal phenotype reveals a function of TDG in maintaining epigenetic stability
Cortázar, D., Kunz, C., Selfridge, J., Lettieri, T., Saito, Y., MacDougall, E., Wirz, A., Schuermann, D., Jacobs, A. L., Siegrist, F., et al. (2011) · Nature · doi:10.1038/nature09672 · Cited by 387
stella Is a Maternal Effect Gene Required for Normal Early Development in Mice
Payer, B., Saitou, M., Barton, S. C., Thresher, R., Dixon, J. P. C., Zahn, D., Colledge, W. H., Carlton, M. B. L., Nakano, T., & Surani, M. A. (2003) · Current Biology · doi:10.1016/j.cub.2003.11.026 · Cited by 372
Self-citationThe role of DNA methylation in setting up chromatin structure during development
Hashimshony, T., Zhang, J., Keshet, I., Bustin, M., & Cedar, H. (2003) · Nature Genetics · doi:10.1038/ng1158 · Cited by 359
Farthing, C. R., Ficz, G., Ng, R. K., Chan, C.-F., Andrews, S., Dean, W., Hemberger, M., & Reik, W. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.1000116 · Cited by 353
Li, H., Rauch, T., Chen, Z.-X., Szabó, P. E., Riggs, A. D., & Pfeifer, G. P. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m513249200 · Cited by 341
Kurimoto, K., Yabuta, Y., Ohinata, Y., Shigeta, M., Yamanaka, K., & Saitou, M. (2008) · Genes & Development · doi:10.1101/gad.1649908 · Cited by 341
Self-citationFunctional cooperation between HP1 and DNMT1 mediates gene silencing
Smallwood, A., Estève, P.-O., Pradhan, S., & Carey, M. (2007) · Genes & Development · doi:10.1101/gad.1536807 · Cited by 339
Vincent, S. D., Dunn, N. R., Sciammas, R., Shapiro-Shalef, M., Davis, M. M., Calame, K., Bikoff, E. K., & Robertson, E. J. (2005) · Development · doi:10.1242/dev.01711 · Cited by 337
Direct estimates of human per nucleotide mutation rates at 20 loci causing mendelian diseases
Kondrashov, A. S. (2003) · Human Mutation · doi:10.1002/humu.10147 · Cited by 336
Enhanced CpG Mutability and Tumorigenesis in MBD4-Deficient Mice
Millar, C. B., Guy, J., Sansom, O. J., Selfridge, J., MacDougall, E., Hendrich, B., Keightley, P. D., Bishop, S. M., Clarke, A. R., & Bird, A. (2002) · Science · doi:10.1126/science.1073354 · Cited by 328
Aapola, U., Shibuya, K., Scott, H. S., Ollila, J., Vihinen, M., Heino, M., Shintani, A., Kawasaki, K., Minoshima, S., Krohn, K., et al. (2000) · Genomics · doi:10.1006/geno.2000.6168 · Cited by 317
Methylation levels of maternal and paternal genomes during preimplantation development
HOWLETT, S. K., & REIK, W. (1991) · Development · doi:10.1242/dev.113.1.119 · Cited by 313
The p27 catalytic subunit of the apolipoprotein B mRNA editing enzyme is a cytidine deaminase.
Navaratnam, N., Morrison, J. R., Bhattacharya, S., Patel, D., Funahashi, T., Giannoni, F., Teng, B. B., Davidson, N. O., & Scott, J. (1993) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)36836-x · Cited by 293
Meiotic and epigenetic defects in Dnmt3L-knockout mouse spermatogenesis
Webster, K. E., O'Bryan, M. K., Fletcher, S., Crewther, P. E., Aapola, U., Craig, J., Harrison, D. K., Aung, H., Phutikanit, N., Lyle, R., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0500702102 · Cited by 290
A role for the elongator complex in zygotic paternal genome demethylation
Okada, Y., Yamagata, K., Hong, K., Wakayama, T., & Zhang, Y. (2010) · Nature · doi:10.1038/nature08732 · Cited by 266
Global hypomethylation of the genome in XX embryonic stem cells
Zvetkova, I., Apedaile, A., Ramsahoye, B., Mermoud, J. E., Crompton, L. A., John, R., Feil, R., & Brockdorff, N. (2005) · Nature Genetics · doi:10.1038/ng1663 · Cited by 247
Dynamic link of DNA demethylation, DNA strand breaks and repair in mouse zygotes
Wossidlo, M., Arand, J., Sebastiano, V., Lepikhov, K., Boiani, M., Reinhardt, R., Schöler, H., & Walter, J. (2010) · The EMBO Journal · doi:10.1038/emboj.2010.80 · Cited by 244
DNA methylation in ES cells requires the lysine methyltransferase G9a but not its catalytic activity
Dong, K. B., Maksakova, I. A., Mohn, F., Leung, D., Appanah, R., Lee, S., Yang, H. W., Lam, L. L., Mager, D. L., Schübeler, D., et al. (2008) · The EMBO Journal · doi:10.1038/emboj.2008.193 · Cited by 242
Tomizawa, S.-I., Kobayashi, H., Watanabe, T., Andrews, S., Hata, K., Kelsey, G., & Sasaki, H. (2011) · Development · doi:10.1242/dev.061416 · Cited by 241
TET Family Proteins and Their Role in Stem Cell Differentiation and Transformation
Cimmino, L., Abdel-Wahab, O., Levine, R. L., & Aifantis, I. (2011) · Cell Stem Cell · doi:10.1016/j.stem.2011.08.007 · Cited by 234
Evolution of imprinting mechanisms: the battle of the sexes begins in the zygote
Reik, W., & Walter, J. (2001) · Nature Genetics · doi:10.1038/85804 · Cited by 232
McrBC: a multisubunit GTP-dependent restriction endonuclease
Sutherland, E., Coe, L., & Raleigh, E. A. (1992) · Journal of Molecular Biology · doi:10.1016/0022-2836(92)90925-a · Cited by 223
X Chromosome Reactivation Initiates in Nascent Primordial Germ Cells in Mice
Sugimoto, M., & Abe, K. (2007) · PLoS Genetics · doi:10.1371/journal.pgen.0030116 · Cited by 214
UHRF1 binds G9a and participates in p21 transcriptional regulation in mammalian cells
Kim, J. K., Estève, P.-O., Jacobsen, S. E., & Pradhan, S. (2009) · Nucleic Acids Research · doi:10.1093/nar/gkn961 · Cited by 209
Meilinger, D., Fellinger, K., Bultmann, S., Rothbauer, U., Bonapace, I. M., Klinkert, W. E. F., Spada, F., & Leonhardt, H. (2009) · EMBO reports · doi:10.1038/embor.2009.201 · Cited by 194
Wylie, C. C. (1980) · Nature · doi:10.1038/283509a0 · Cited by 191
Recognition of 5-Hydroxymethylcytosine by the Uhrf1 SRA Domain
Frauer, C., Hoffmann, T., Bultmann, S., Casa, V., Cardoso, M. C., Antes, I., & Leonhardt, H. (2011) · PLoS ONE · doi:10.1371/journal.pone.0021306 · Cited by 180
Roles for Dnmt3b in mammalian development: a mouse model for the ICF syndrome
Ueda, Y., Okano, M., Williams, C., Chen, T., Georgopoulos, K., & Li, E. (2006) · Development · doi:10.1242/dev.02293 · Cited by 171
The multi-domain protein Np95 connects DNA methylation and histone modification
Rottach, A., Frauer, C., Pichler, G., Bonapace, I. M., Spada, F., & Leonhardt, H. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkp1152 · Cited by 164
Transgenerational epigenetic inheritance in health and disease
Whitelaw, N. C., & Whitelaw, E. (2008) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2008.07.001 · Cited by 164
Genome-Wide Profiling of DNA Methylation Reveals Transposon Targets of CHROMOMETHYLASE3
Tompa, R., McCallum, C. M., Delrow, J., Henikoff, J. G., van Steensel, B., & Henikoff, S. (2002) · Current Biology · doi:10.1016/s0960-9822(01)00622-4 · Cited by 161
GADD45A Does Not Promote DNA Demethylation
Jin, S.-G., Guo, C., & Pfeifer, G. P. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.1000013 · Cited by 161
Oda, M., Glass, J. L., Thompson, R. F., Mo, Y., Olivier, E. N., Figueroa, M. E., Selzer, R. R., Richmond, T., Zhang, X., Dannenberg, L. O., et al. (2009) · Nucleic Acids Research · doi:10.1093/nar/gkp260 · Cited by 157
Hirano, K., Young, S. G., Farese, R. V., Ng, J. K., Sande, E., Warburton, C., Powell-Braxton, L., & Davidson, N. O. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.17.9887 · Cited by 155
Heterochromatin establishment in the context of genome-wide epigenetic reprogramming
Probst, A. V., & Almouzni, G. (2011) · Trends in Genetics · doi:10.1016/j.tig.2011.02.002 · Cited by 153
Tam, P., Zhou, S. X., & Tan, S. (1994) · Development · doi:10.1242/dev.120.10.2925 · Cited by 126
Dnmt1 Expression in Pre- and Postimplantation Embryogenesis and the Maintenance of IAP Silencing
Gaudet, F., Rideout, W. M., Meissner, A., Dausman, J. A., Leonhardt, H., & Jaenisch, R. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.4.1640-1648.2004 · Cited by 121
Oda, M., Yamagiwa, A., Yamamoto, S., Nakayama, T., Tsumura, A., Sasaki, H., Nakao, K., Li, E., & Okano, M. (2006) · Genes & Development · doi:10.1101/gad.1470906 · Cited by 105
AID to overcome the limitations of genomic information
Honjo, T., Nagaoka, H., Shinkura, R., & Muramatsu, M. (2005) · Nature Immunology · doi:10.1038/ni1218 · Cited by 102
Fujimori, A., Matsuda, Y., Takemoto, Y., Hashimoto, Y., Kubo, E., Araki, R., Fukumura, R., Mita, K., Tatsumi, K., & Muto, M. (1998) · Mammalian Genome · doi:10.1007/s003359900920 · Cited by 96
Kobayashi, H., Suda, C., Abe, T., Kohara, Y., Ikemura, T., & Sasaki, H. (2006) · Cytogenetic and Genome Research · doi:10.1159/000090824 · Cited by 89
Resetting the Epigenome beyond Pluripotency in the Germline
Hayashi, K., & Surani, M. A. (2009) · Cell stem cell · doi:10.1016/j.stem.2009.05.007 · 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
Morrison, J. R., Pászty, C., Stevens, M. E., Hughes, S., Forte, T., Scott, J., & Rubin, E. M. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.14.7154 · Cited by 86
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 86
Conserved DNA methylation inGadd45a-/-mice
Engel, N., Tront, J. S., Erinle, T., Nguyen, N. H., Latham, K. E., Sapienza, C., Hoffman‐Liebermann, B., & Liebermann, D. A. (2009) · Epigenetics · doi:10.4161/epi.4.2.7858 · Cited by 86
Ziegler-Birling, C., Helmrich, A., Tora, L., & Torres‐Padilla, M. (2009) · The International Journal of Developmental Biology · doi:10.1387/ijdb.082707cz · Cited by 85
Methylation protects cytidines from AID-mediated deamination
Larijani, M., Frieder, D., Sonbuchner, T. M., Bransteitter, R., Goodman, M. G., Bouhassira, E. E., Scharff, M. D., & Martín, A. (2004) · Molecular Immunology · doi:10.1016/j.molimm.2004.09.007 · Cited by 76
Hu, X. V., Rodrigues, T. M. A., Tao, H., Baker, R. K., Miraglia, L. J., Orth, A. P., Lyons, G. E., Schultz, P. G., & Wu, X. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1009025107 · Cited by 75
Chromosome silencing mechanisms in X-chromosome inactivation: unknown unknowns
Brockdorff, N. (2011) · Development · doi:10.1242/dev.065276 · Cited by 73
Branco, M. R., Oda, M., & Reik, W. (2008) · Genes & Development · doi:10.1101/gad.1690508 · Cited by 72
Confounded cytosine! Tinkering and the evolution of DNA
Poole, A. M., Penny, D., & Sjöberg, B. (2001) · Nature Reviews Molecular Cell Biology · doi:10.1038/35052091 · Cited by 68
Burdzy, A. (2002) · Nucleic Acids Research · doi:10.1093/nar/gkf520 · Cited by 43
Hypomethylation of paternal DNA in the late mouse zygote is not essential for development
Polański, Z., Motosugi, N., Tsurumi, C., et al. (2008) · The International Journal of Developmental Biology · doi:10.1387/ijdb.072347zp · Cited by 40
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Metadata
- Authors
- Saitou, M., Kagiwada, S., & Kurimoto, K.
- Venue
- Development
- Publisher
- The Company of Biologists
- Published
- 2012-01-01
- Volume
- 139
- Issue
- 1
- Pages
- 15-31
- ISSN
- 0950-1991 (ISSN-L)
- 1477-9129
- OpenAlex
- W2067102637
- Cited by
- 414
- References
- 187
- FWCI
- 11.87
- Type
- journal article
- Language
- en
- Open access
- closed
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Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.