메뉴 건너뛰기




Volumn 77, Issue 2, 2010, Pages 105-113

DNA methylation in early development

Author keywords

[No Author keywords available]

Indexed keywords

CYTOSINE; DNA; DNA METHYLTRANSFERASE; DNA METHYLTRANSFERASE 1; DNA METHYLTRANSFERASE 3B;

EID: 73249144150     PISSN: 1040452X     EISSN: 10982795     Source Type: Journal    
DOI: 10.1002/mrd.21118     Document Type: Review
Times cited : (108)

References (84)
  • 1
    • 53849110899 scopus 로고    scopus 로고
    • Fragile X syndrome: Loss of local mRNA regulation alters synaptic development and function
    • Bassell GJ, Warren ST. 2008. Fragile X syndrome: Loss of local mRNA regulation alters synaptic development and function. Neuron 60:201-214.
    • (2008) Neuron , vol.60 , pp. 201-214
    • Bassell, G.J.1    Warren, S.T.2
  • 2
    • 0028786951 scopus 로고
    • Loss of methylation activates Xist in somatic but not in embryonic cells
    • Beard C, Li E, Jaenisch R. 1995. Loss of methylation activates Xist in somatic but not in embryonic cells. Genes Dev 9:2325-2334.
    • (1995) Genes Dev , vol.9 , pp. 2325-2334
    • Beard, C.1    Li, E.2    Jaenisch, R.3
  • 4
    • 0033601073 scopus 로고    scopus 로고
    • Methylation-induced repression-Belts, braces, and chromatin
    • Bird AP, Wolffe AP. 1999. Methylation-induced repression-Belts, braces, and chromatin. Cell 99:451-454.
    • (1999) Cell , vol.99 , pp. 451-454
    • Bird, A.P.1    Wolffe, A.P.2
  • 6
    • 0035930660 scopus 로고    scopus 로고
    • Dnmt3L and the establishment of maternal genomic imprints
    • Bourc'his D, Xu GL, Lin CS, Bollman B, Bestor TH. 2001. Dnmt3L and the establishment of maternal genomic imprints. Science 294:2536-2539.
    • (2001) Science , vol.294 , pp. 2536-2539
    • Bourc'his, D.1    Xu, G.L.2    Lin, C.S.3    Bollman, B.4    Bestor, T.H.5
  • 8
    • 0033523760 scopus 로고    scopus 로고
    • DNA methyltransferase is actively retained in the cytoplasm during early development
    • Cardoso MC, Leonhardt H. 1999. DNA methyltransferase is actively retained in the cytoplasm during early development. J Cell Biol 147:25-32.
    • (1999) J Cell Biol , vol.147 , pp. 25-32
    • Cardoso, M.C.1    Leonhardt, H.2
  • 9
    • 0034769764 scopus 로고    scopus 로고
    • CpG binding protein is crucial for early embryonic development
    • Carlone DL, Skalnik DG. 2001. CpG binding protein is crucial for early embryonic development. Mol Cell Biol 21:7601-7606.
    • (2001) Mol Cell Biol , vol.21 , pp. 7601-7606
    • Carlone, D.L.1    Skalnik, D.G.2
  • 10
    • 20344396373 scopus 로고    scopus 로고
    • Reduced genomic cytosine methylation and defective cellular differentiation in embryonic stem cells lacking CpG binding protein
    • Carlone DL, Lee JH, Young SR, Dobrota E, Butler JS, Ruiz J, Skalnik DG. 2005. Reduced genomic cytosine methylation and defective cellular differentiation in embryonic stem cells lacking CpG binding protein. Mol Cell Biol 25:4881-4891.
    • (2005) Mol Cell Biol , vol.25 , pp. 4881-4891
    • Carlone, D.L.1    Lee, J.H.2    Young, S.R.3    Dobrota, E.4    Butler, J.S.5    Ruiz, J.6    Skalnik, D.G.7
  • 11
    • 0027096740 scopus 로고
    • Properties and localization of DNA methyltransferase in preimplantation mouse embryos: Implications for genomic imprinting
    • Carlson LL, Page AW, Bestor TH. 1992. Properties and localization of DNA methyltransferase in preimplantation mouse embryos: Implications for genomic imprinting. Genes Dev 6:2536-2541.
    • (1992) Genes Dev , vol.6 , pp. 2536-2541
    • Carlson, L.L.1    Page, A.W.2    Bestor, T.H.3
  • 12
    • 35648978121 scopus 로고    scopus 로고
    • The story of Rett syndrome: From clinic to neurobiology
    • Chahrour M, Zoghbi HY. 2007. The story of Rett syndrome: From clinic to neurobiology. Neuron 56:422-437.
    • (2007) Neuron , vol.56 , pp. 422-437
    • Chahrour, M.1    Zoghbi, H.Y.2
  • 13
    • 0021139979 scopus 로고
    • Cell lineage-specific undermethylation of mouse repetitive DNA
    • Chapman V, Forrester L, Sanford J, Hastie N, Rossant J. 1984. Cell lineage-specific undermethylation of mouse repetitive DNA. Nature 307:284-286.
    • (1984) Nature , vol.307 , pp. 284-286
    • Chapman, V.1    Forrester, L.2    Sanford, J.3    Hastie, N.4    Rossant, J.5
  • 14
    • 0037168587 scopus 로고    scopus 로고
    • TheDNAmethyltransferase-like protein DNMT3L stimulates de novo methylation by Dnmt3a
    • Chedin F, Lieber MR, Hsieh CL. 2002. TheDNAmethyltransferase-like protein DNMT3L stimulates de novo methylation by Dnmt3a. Proc Natl Acad Sci USA 99:16916-16921.
    • (2002) Proc Natl Acad Sci USA , vol.99 , pp. 16916-16921
    • Chedin, F.1    Lieber, M.R.2    Hsieh, C.L.3
  • 15
    • 33847293264 scopus 로고    scopus 로고
    • Complete inactivation of DNMT1 leads to mitotic catastrophe in human cancer cells
    • Chen T, Hevi S, Gay F, Tsujimoto N, He T, Zhang B, Ueda Y, Li E. 2007. Complete inactivation of DNMT1 leads to mitotic catastrophe in human cancer cells. Nat Genet 39:391-396.
    • (2007) Nat Genet , vol.39 , pp. 391-396
    • Chen, T.1    Hevi, S.2    Gay, F.3    Tsujimoto, N.4    He, T.5    Zhang, B.6    Ueda, Y.7    Li, E.8
  • 16
    • 0030034051 scopus 로고    scopus 로고
    • XIST RNA paints the inactive X chromosome at interphase: Evidence for a novelRNAinvolved in nuclear/chromosome structure
    • Clemson CM, McNeil JA, Willard HF, Lawrence JB. 1996. XIST RNA paints the inactive X chromosome at interphase: Evidence for a novelRNAinvolved in nuclear/chromosome structure. J Cell Biol 132:259-275.
    • (1996) J Cell Biol , vol.132 , pp. 259-275
    • Clemson, C.M.1    McNeil, J.A.2    Willard, H.F.3    Lawrence, J.B.4
  • 17
    • 0032905253 scopus 로고    scopus 로고
    • Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells
    • Coffee B, Zhang F, Warren ST, Reines D. 1999. Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells. Nat Genet 22:98-101.
    • (1999) Nat Genet , vol.22 , pp. 98-101
    • Coffee, B.1    Zhang, F.2    Warren, S.T.3    Reines, D.4
  • 18
    • 0035858882 scopus 로고    scopus 로고
    • Synergism of Xist RNA, DNA methylation, and histone hypoacetylation in maintaining X chromosome inactivation
    • Csankovszki G, Nagy A, Jaenisch R. 2001. Synergism of Xist RNA, DNA methylation, and histone hypoacetylation in maintaining X chromosome inactivation. J Cell Biol 153:773-784.
    • (2001) J Cell Biol , vol.153 , pp. 773-784
    • Csankovszki, G.1    Nagy, A.2    Jaenisch, R.3
  • 19
    • 0032694084 scopus 로고    scopus 로고
    • DNA methylation is the primary silencing mechanism for a set of germ line- and tumor-specific genes with a CpG-rich promoter
    • De Smet C, Lurquin C, Lethe B, Martelange V, Boon T. 1999. DNA methylation is the primary silencing mechanism for a set of germ line- and tumor-specific genes with a CpG-rich promoter. Mol Cell Biol 19:7327-7335.
    • (1999) Mol Cell Biol , vol.19 , pp. 7327-7335
    • De Smet, C.1    Lurquin, C.2    Lethe, B.3    Martelange, V.4    Boon, T.5
  • 20
    • 0035923602 scopus 로고    scopus 로고
    • Conservation of methylation reprogramming in mammalian development: Aberrant reprogramming in cloned embryos
    • Dean W, Santos F, Stojkovic M, Zakhartchenko V, Walter J, Wolf E, Reik W. 2001. Conservation of methylation reprogramming in mammalian development: Aberrant reprogramming in cloned embryos. Proc Natl Acad Sci USA 98:13734-13738.
    • (2001) Proc Natl Acad Sci USA , vol.98 , pp. 13734-13738
    • Dean, W.1    Santos, F.2    Stojkovic, M.3    Zakhartchenko, V.4    Walter, J.5    Wolf, E.6    Reik, W.7
  • 21
    • 0035890090 scopus 로고    scopus 로고
    • Lsh, a member of the SNF2 family, is required for genome-wide methylation
    • Dennis K, Fan T, Geiman T, Yan Q, Muegge K. 2001. Lsh, a member of the SNF2 family, is required for genome-wide methylation. Genes Dev 15:2940-2944.
    • (2001) Genes Dev , vol.15 , pp. 2940-2944
    • Dennis, K.1    Fan, T.2    Geiman, T.3    Yan, Q.4    Muegge, K.5
  • 22
    • 0026751517 scopus 로고
    • Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development
    • Devys D, Biancalana V, Rousseau F, Boue J, Mandel JL, Oberle I. 1992. Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development. Am J Med Genet 43:208-216.
    • (1992) Am J Med Genet , vol.43 , pp. 208-216
    • Devys, D.1    Biancalana, V.2    Rousseau, F.3    Boue, J.4    Mandel, J.L.5    Oberle, I.6
  • 23
    • 33748998743 scopus 로고    scopus 로고
    • Identification of DNMT1 (DNA methyl-transferase 1) hypomorphs in somatic knockouts suggests an essential role for DNMT1 in cell survival
    • Egger G, Jeong S, Escobar SG, Cortez CC, Li TW, Saito Y, Yoo CB, Jones PA, Liang G. 2006. Identification of DNMT1 (DNA methyl-transferase 1) hypomorphs in somatic knockouts suggests an essential role for DNMT1 in cell survival. Proc Natl Acad Sci USA 103:14080-14085.
    • (2006) Proc Natl Acad Sci USA , vol.103 , pp. 14080-14085
    • Egger, G.1    Jeong, S.2    Escobar, S.G.3    Cortez, C.C.4    Li, T.W.5    Saito, Y.6    Yoo, C.B.7    Jones, P.A.8    Liang, G.9
  • 24
    • 42649130058 scopus 로고    scopus 로고
    • ICF, an immunodeficiency syndrome: DNA methyltransferase 3B involvement, chromosome anomalies, and gene dysregulation
    • Ehrlich M, Sanchez C, Shao C, Nishiyama R, Kehrl J, Kuick R, Kubota T, Hanash SM. 2008. ICF, an immunodeficiency syndrome: DNA methyltransferase 3B involvement, chromosome anomalies, and gene dysregulation. Autoimmunity 41:253-271.
    • (2008) Autoimmunity , vol.41 , pp. 253-271
    • Ehrlich, M.1    Sanchez, C.2    Shao, C.3    Nishiyama, R.4    Kehrl, J.5    Kuick, R.6    Kubota, T.7    Hanash, S.M.8
  • 25
    • 45349086923 scopus 로고    scopus 로고
    • Farthing CR, Ficz G, Ng RK, Chan CF, Andrews S, Dean W, Hemberger M, Reik W. 2008. Global mapping of DNA methylation in mouse promoters reveals epigenetic reprogramming of pluripotency genes. PLoS Genet 4:e1000116.
    • Farthing CR, Ficz G, Ng RK, Chan CF, Andrews S, Dean W, Hemberger M, Reik W. 2008. Global mapping of DNA methylation in mouse promoters reveals epigenetic reprogramming of pluripotency genes. PLoS Genet 4:e1000116.
  • 26
    • 38649126918 scopus 로고    scopus 로고
    • Promoter CpG methylation contributes to ES cell gene regulation in parallel with Oct4/Nanog, PcG complex, and histone H3 K4/K27 trimethylation
    • Fouse SD, Shen Y, Pellegrini M, Cole S, Meissner A, Van Neste L, Jaenisch R, Fan G. 2008. Promoter CpG methylation contributes to ES cell gene regulation in parallel with Oct4/Nanog, PcG complex, and histone H3 K4/K27 trimethylation. Cell Stem Cell 2:160-169.
    • (2008) Cell Stem Cell , vol.2 , pp. 160-169
    • Fouse, S.D.1    Shen, Y.2    Pellegrini, M.3    Cole, S.4    Meissner, A.5    Van Neste, L.6    Jaenisch, R.7    Fan, G.8
  • 28
    • 0034712755 scopus 로고    scopus 로고
    • Lsh, an SNF2/helicase family member, is required for proliferation of mature T lymphocytes
    • Geiman TM, Muegge K. 2000. Lsh, an SNF2/helicase family member, is required for proliferation of mature T lymphocytes. Proc Natl Acad Sci USA 97:4772-4777.
    • (2000) Proc Natl Acad Sci USA , vol.97 , pp. 4772-4777
    • Geiman, T.M.1    Muegge, K.2
  • 30
    • 0029128827 scopus 로고
    • Syndromal mental retardation due to mutations in a regulator of gene expression
    • Gibbons RJ, Picketts DJ, Higgs DR. 1995. Syndromal mental retardation due to mutations in a regulator of gene expression. Hum Mol Genet 4:1705-1709.
    • (1995) Hum Mol Genet , vol.4 , pp. 1705-1709
    • Gibbons, R.J.1    Picketts, D.J.2    Higgs, D.R.3
  • 31
    • 0034069652 scopus 로고    scopus 로고
    • Mutations in ATRX, encoding a SWI/ SNF-like protein, cause diverse changes in the pattern of DNA methylation
    • Gibbons RJ, McDowell TL, Raman S, O'Rourke DM, Garrick D, Ayyub H, Higgs DR. 2000. Mutations in ATRX, encoding a SWI/ SNF-like protein, cause diverse changes in the pattern of DNA methylation. Nat Genet 24:368-371.
    • (2000) Nat Genet , vol.24 , pp. 368-371
    • Gibbons, R.J.1    McDowell, T.L.2    Raman, S.3    O'Rourke, D.M.4    Garrick, D.5    Ayyub, H.6    Higgs, D.R.7
  • 33
    • 17144369504 scopus 로고    scopus 로고
    • Mechanism of stimulation of catalytic activity of Dnmt3A and Dnmt3B DNA-(cytosine-C5)- methyltransferases by Dnmt3L
    • Gowher H, Liebert K, Hermann A, Xu G, Jeltsch A. 2005. Mechanism of stimulation of catalytic activity of Dnmt3A and Dnmt3B DNA-(cytosine-C5)- methyltransferases by Dnmt3L. J Biol Chem 280:13341-13348.
    • (2005) J Biol Chem , vol.280 , pp. 13341-13348
    • Gowher, H.1    Liebert, K.2    Hermann, A.3    Xu, G.4    Jeltsch, A.5
  • 34
    • 33748107733 scopus 로고    scopus 로고
    • Methylation dynamics in the early mammalian embryo: Implications of genome reprogramming defects for development
    • Haaf T. 2006. Methylation dynamics in the early mammalian embryo: Implications of genome reprogramming defects for development. Curr Top Microbiol Immunol 310:13-22.
    • (2006) Curr Top Microbiol Immunol , vol.310 , pp. 13-22
    • Haaf, T.1
  • 36
    • 2342437315 scopus 로고    scopus 로고
    • Epigenetic control of mouse Oct-4 gene expression in embryonic stem cells and trophoblast stem cells
    • Hattori N, Nishino K, Ko YG, Ohgane J, Tanaka S, Shiota K. 2004. Epigenetic control of mouse Oct-4 gene expression in embryonic stem cells and trophoblast stem cells. J Biol Chem 279: 17063-17069.
    • (2004) J Biol Chem , vol.279 , pp. 17063-17069
    • Hattori, N.1    Nishino, K.2    Ko, Y.G.3    Ohgane, J.4    Tanaka, S.5    Shiota, K.6
  • 38
    • 33746069681 scopus 로고    scopus 로고
    • Dosage compensation in mammals: Fine-tuning the expression of the X chromosome
    • Heard E, Disteche CM. 2006. Dosage compensation in mammals: Fine-tuning the expression of the X chromosome. Genes Dev 20:1848-1867.
    • (2006) Genes Dev , vol.20 , pp. 1848-1867
    • Heard, E.1    Disteche, C.M.2
  • 39
    • 0025800593 scopus 로고
    • Methylation levels of maternal and paternal genomes during preimplantation development
    • Howlett SK, Reik W. 1991. Methylation levels of maternal and paternal genomes during preimplantation development. Development 113:119-127.
    • (1991) Development , vol.113 , pp. 119-127
    • Howlett, S.K.1    Reik, W.2
  • 44
    • 32344450824 scopus 로고    scopus 로고
    • Genomic DNA methylation: The mark and its mediators
    • Klose RJ, Bird AP. 2006. Genomic DNA methylation: The mark and its mediators. Trends Biochem Sci 31:89-97.
    • (2006) Trends Biochem Sci , vol.31 , pp. 89-97
    • Klose, R.J.1    Bird, A.P.2
  • 45
    • 0037298161 scopus 로고    scopus 로고
    • Resistance of IAPs to methylation reprogramming may provide a mechanism for epigenetic inheritance in the mouse
    • Lane N, Dean W, Erhardt S, Hajkova P, Surani A, Walter J, Reik W. 2003. Resistance of IAPs to methylation reprogramming may provide a mechanism for epigenetic inheritance in the mouse. Genesis 35:88-93.
    • (2003) Genesis , vol.35 , pp. 88-93
    • Lane, N.1    Dean, W.2    Erhardt, S.3    Hajkova, P.4    Surani, A.5    Walter, J.6    Reik, W.7
  • 46
    • 37449033507 scopus 로고    scopus 로고
    • DNA methylation in mouse embryonic stem cells and development
    • Latham T, Gilbert N, Ramsahoye B. 2008. DNA methylation in mouse embryonic stem cells and development. Cell Tissue Res 331:31-55.
    • (2008) Cell Tissue Res , vol.331 , pp. 31-55
    • Latham, T.1    Gilbert, N.2    Ramsahoye, B.3
  • 49
    • 0026439115 scopus 로고
    • A targeting sequence directs DNA methyltransferase to sites of DNA replication in mammalian nuclei
    • Leonhardt H, Page AW, Weier HU, Bestor TH. 1992. A targeting sequence directs DNA methyltransferase to sites of DNA replication in mammalian nuclei. Cell 71:865-873.
    • (1992) Cell , vol.71 , pp. 865-873
    • Leonhardt, H.1    Page, A.W.2    Weier, H.U.3    Bestor, T.H.4
  • 50
    • 0026708177 scopus 로고
    • Targeted mutation of the DNA methyltransferase gene results in embryonic lethality
    • Li E, Bestor TH, Jaenisch R. 1992. Targeted mutation of the DNA methyltransferase gene results in embryonic lethality. Cell 69: 915-926.
    • (1992) Cell , vol.69 , pp. 915-926
    • Li, E.1    Bestor, T.H.2    Jaenisch, R.3
  • 52
    • 0033804210 scopus 로고    scopus 로고
    • Spatial separation of parental genomes during mouse interspecific (Mus musculus x M. spretus) spermiogenesis
    • Mayer W, Fundele R, Haaf T. 2000a. Spatial separation of parental genomes during mouse interspecific (Mus musculus x M. spretus) spermiogenesis. Chromosome Res 8:555-558.
    • (2000) Chromosome Res , vol.8 , pp. 555-558
    • Mayer, W.1    Fundele, R.2    Haaf, T.3
  • 55
    • 51649129596 scopus 로고    scopus 로고
    • Lineage-specific polycomb targets and de novo DNA methylation define restriction and potential of neuronal progenitors
    • Mohn F, Weber M, Rebhan M, Roloff TC, Richter J, Stadler MB, Bibel M, Schubeler D. 2008. Lineage-specific polycomb targets and de novo DNA methylation define restriction and potential of neuronal progenitors. Mol Cell 30:755-766.
    • (2008) Mol Cell , vol.30 , pp. 755-766
    • Mohn, F.1    Weber, M.2    Rebhan, M.3    Roloff, T.C.4    Richter, J.5    Stadler, M.B.6    Bibel, M.7    Schubeler, D.8
  • 56
    • 0023119242 scopus 로고
    • Temporal and regional changes in DNA methylation in the embryonic, extraembryonic and germ cell lineages during mouse embryo development
    • Monk M, Boubelik M, Lehnert S. 1987. Temporal and regional changes in DNA methylation in the embryonic, extraembryonic and germ cell lineages during mouse embryo development. Development 99:371-382.
    • (1987) Development , vol.99 , pp. 371-382
    • Monk, M.1    Boubelik, M.2    Lehnert, S.3
  • 57
    • 34247095504 scopus 로고    scopus 로고
    • Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation
    • Nagarajan RP, Hogart AR, Gwye Y, Martin MR, LaSalle JM. 2006. Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation. Epigenetics 1:e1-e11.
    • (2006) Epigenetics , vol.1
    • Nagarajan, R.P.1    Hogart, A.R.2    Gwye, Y.3    Martin, M.R.4    LaSalle, J.M.5
  • 59
    • 33847282970 scopus 로고    scopus 로고
    • Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation
    • Nan X, Hou J, Maclean A, Nasir J, Lafuente MJ, Shu X, Kriaucionis S, Bird A. 2007. Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation. Proc Natl Acad Sci USA 104:2709-2714.
    • (2007) Proc Natl Acad Sci USA , vol.104 , pp. 2709-2714
    • Nan, X.1    Hou, J.2    Maclean, A.3    Nasir, J.4    Lafuente, M.J.5    Shu, X.6    Kriaucionis, S.7    Bird, A.8
  • 60
    • 0033615717 scopus 로고    scopus 로고
    • DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development
    • Okano M, Bell DW, Haber DA, Li E. 1999. DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development. Cell 99:247-257.
    • (1999) Cell , vol.99 , pp. 247-257
    • Okano, M.1    Bell, D.W.2    Haber, D.A.3    Li, E.4
  • 61
    • 0031279892 scopus 로고    scopus 로고
    • The pre-implantation ontogeny of the H19 methylation imprint
    • Olek A, Walter J. 1997. The pre-implantation ontogeny of the H19 methylation imprint. Nat Genet 17:275-276.
    • (1997) Nat Genet , vol.17 , pp. 275-276
    • Olek, A.1    Walter, J.2
  • 63
    • 0029956442 scopus 로고    scopus 로고
    • DNA hypomethylation can activate Xist expression and silence X-linked genes
    • Panning B, Jaenisch R. 1996. DNA hypomethylation can activate Xist expression and silence X-linked genes. Genes Dev 10: 1991-2002.
    • (1996) Genes Dev , vol.10 , pp. 1991-2002
    • Panning, B.1    Jaenisch, R.2
  • 65
    • 0035234557 scopus 로고    scopus 로고
    • Genomic imprinting: Parental influence on the genome
    • Reik W, Walter J. 2001. Genomic imprinting: Parental influence on the genome. Nat Rev Genet 2:21-32.
    • (2001) Nat Rev Genet , vol.2 , pp. 21-32
    • Reik, W.1    Walter, J.2
  • 68
    • 1642363256 scopus 로고    scopus 로고
    • DenovoDNAmethylation is dispensable for the initiation and propagation of X chromosome inactivation
    • Sado T, Okano M, Li E, Sasaki H. 2004.DenovoDNAmethylation is dispensable for the initiation and propagation of X chromosome inactivation. Development 131:975-982.
    • (2004) Development , vol.131 , pp. 975-982
    • Sado, T.1    Okano, M.2    Li, E.3    Sasaki, H.4
  • 69
    • 0023503627 scopus 로고
    • Differences in DNA methylation during oogenesis and spermatogenesis and their persistence during early embryogenesis in the mouse
    • Sanford JP, Clark HJ, Chapman VM, Rossant J. 1987. Differences in DNA methylation during oogenesis and spermatogenesis and their persistence during early embryogenesis in the mouse. Genes Dev 1:1039-1046.
    • (1987) Genes Dev , vol.1 , pp. 1039-1046
    • Sanford, J.P.1    Clark, H.J.2    Chapman, V.M.3    Rossant, J.4
  • 70
    • 65349135493 scopus 로고    scopus 로고
    • Xist gene regulation at the onset of X inactivation
    • Senner CE, Brockdorff N. 2009. Xist gene regulation at the onset of X inactivation. Curr Opin Genet Dev 19:122-126.
    • (2009) Curr Opin Genet Dev , vol.19 , pp. 122-126
    • Senner, C.E.1    Brockdorff, N.2
  • 74
    • 48549092573 scopus 로고    scopus 로고
    • Soper SF, van der HeijdenGW,Hardiman TC, Goodheart M, Martin SL, de Boer P, Bortvin A. 2008. Mouse maelstrom, a component of nuage, is essential for spermatogenesis and transposon repression in meiosis. Dev Cell 15:285-297.
    • Soper SF, van der HeijdenGW,Hardiman TC, Goodheart M, Martin SL, de Boer P, Bortvin A. 2008. Mouse maelstrom, a component of nuage, is essential for spermatogenesis and transposon repression in meiosis. Dev Cell 15:285-297.
  • 75
    • 3042641718 scopus 로고    scopus 로고
    • DNMT3L stimulates the DNA methylation activity of Dnmt3a and Dnmt3b through a direct interaction
    • Suetake I, Shinozaki F, Miyagawa J, Takeshima H, Tajima S. 2004. DNMT3L stimulates the DNA methylation activity of Dnmt3a and Dnmt3b through a direct interaction. J Biol Chem 279: 27816-27823.
    • (2004) J Biol Chem , vol.279 , pp. 27816-27823
    • Suetake, I.1    Shinozaki, F.2    Miyagawa, J.3    Takeshima, H.4    Tajima, S.5
  • 78
    • 0030802395 scopus 로고    scopus 로고
    • A 5' 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development
    • Tremblay KD, Duran KL, Bartolomei MS. 1997. A 5' 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development. Mol Cell Biol 17:4322-4329.
    • (1997) Mol Cell Biol , vol.17 , pp. 4322-4329
    • Tremblay, K.D.1    Duran, K.L.2    Bartolomei, M.S.3
  • 79
    • 0034123060 scopus 로고    scopus 로고
    • Methyl-CpG-binding protein 2 mutations in Rett syndrome
    • Van den Veyver IB, Zoghbi HY. 2000. Methyl-CpG-binding protein 2 mutations in Rett syndrome. Curr Opin Genet Dev 10:275-279.
    • (2000) Curr Opin Genet Dev , vol.10 , pp. 275-279
    • Van den Veyver, I.B.1    Zoghbi, H.Y.2
  • 80
    • 0036803302 scopus 로고    scopus 로고
    • Stage- and cell-specific expression of Dnmt3a and Dnmt3b during embryogenesis
    • Watanabe D, Suetake I, Tada T, Tajima S. 2002. Stage- and cell-specific expression of Dnmt3a and Dnmt3b during embryogenesis. Mech Dev 118:187-190.
    • (2002) Mech Dev , vol.118 , pp. 187-190
    • Watanabe, D.1    Suetake, I.2    Tada, T.3    Tajima, S.4
  • 81
    • 34047116826 scopus 로고    scopus 로고
    • Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome
    • Weber M, Hellmann I, Stadler MB, Ramos L, Paabo S, Rebhan M, Schubeler D. 2007. Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome. Nat Genet 39:457-466.
    • (2007) Nat Genet , vol.39 , pp. 457-466
    • Weber, M.1    Hellmann, I.2    Stadler, M.B.3    Ramos, L.4    Paabo, S.5    Rebhan, M.6    Schubeler, D.7
  • 83
    • 0031577334 scopus 로고    scopus 로고
    • DNA(cytosine-5)- methyltransferases in mouse cells and tissues. Studies with a mechanism-based probe
    • Yoder JA,SomanNS, VerdineGL,Bestor TH.1997.DNA(cytosine-5)- methyltransferases in mouse cells and tissues. Studies with a mechanism-based probe. J Mol Biol 270:385-395.
    • (1997) J Mol Biol , vol.270 , pp. 385-395
    • Yoder, J.A.1    Soman, N.S.2    Verdine, G.L.3    Bestor, T.H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.