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Volumn 13, Issue 5, 2005, Pages 641-648

Differential epigenetic modifications in the FMR1 gene of the fragile X syndrome after reactivating pharmacological treatments

Author keywords

Chromatin immunoprecipitation; Epigenetic modifications; Fragile X syndrome; Reactivating treatments; Real time PCR

Indexed keywords

5 AZA 2' DEOXYCYTIDINE; ACETYLCARNITINE; DNA; FRAGILE X MENTAL RETARDATION PROTEIN; HISTONE H3; HISTONE H4; LYSINE;

EID: 18844398832     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5201393     Document Type: Article
Times cited : (90)

References (27)
  • 1
    • 0026345716 scopus 로고
    • Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
    • Fu YH, Kuhl DF, Pizzuti A et al: Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox. Cell 1991; 67: 1047-1058.
    • (1991) Cell , vol.67 , pp. 1047-1058
    • Fu, Y.H.1    Kuhl, D.F.2    Pizzuti, A.3
  • 2
    • 0025905795 scopus 로고
    • Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting lenght variation in fragile X syndrome
    • Verkerk AJMH, Pieretti M, Sutcliffe JS et al: Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting lenght variation in fragile X syndrome. Cell 1991; 65: 905-914.
    • (1991) Cell , vol.65 , pp. 905-914
    • Verkerk, A.J.M.H.1    Pieretti, M.2    Sutcliffe, J.S.3
  • 3
    • 0028989063 scopus 로고
    • Translational suppression by trinucleotide repeat expansion at FMR1
    • Feng Y, Zhang F, Lokey LK et al: Translational suppression by trinucleotide repeat expansion at FMR1. Science 1995; 268: 731-734.
    • (1995) Science , vol.268 , pp. 731-734
    • Feng, Y.1    Zhang, F.2    Lokey, L.K.3
  • 4
    • 0025833298 scopus 로고
    • Absence of expression of the FMR-1 gene in fragile X syndrome
    • Pieretti M, Zhang F, Fu YH et al: Absence of expression of the FMR-1 gene in fragile X syndrome. Cell 1991; 66: 817-822.
    • (1991) Cell , vol.66 , pp. 817-822
    • Pieretti, M.1    Zhang, F.2    Fu, Y.H.3
  • 5
    • 18044379515 scopus 로고    scopus 로고
    • Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome
    • Brown V, Jin P, Ceman S et al: Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome. Cell 2001; 107: 477-487.
    • (2001) Cell , vol.107 , pp. 477-487
    • Brown, V.1    Jin, P.2    Ceman, S.3
  • 6
    • 1942467797 scopus 로고    scopus 로고
    • Molecular insights into mental retardation: Multiple functions for the fragile X mental retardation protein?
    • Zalfa F, Bagni C: Molecular insights into mental retardation: multiple functions for the fragile X mental retardation protein? Curr Issues Mol Biol 2004; 6: 73-88.
    • (2004) Curr. Issues Mol. Biol. , vol.6 , pp. 73-88
    • Zalfa, F.1    Bagni, C.2
  • 7
    • 0028264043 scopus 로고
    • High functioning fragile X males: Demonstration of an unmethylated fully expanded FMR1 mutation associated with protein expression
    • Hagerman RJ, Hull CE, Safanda JF et al: High functioning fragile X males: demonstration of an unmethylated fully expanded FMR1 mutation associated with protein expression. Am J Med Genet 1994; 51: 298-308.
    • (1994) Am. J. Med. Genet. , vol.51 , pp. 298-308
    • Hagerman, R.J.1    Hull, C.E.2    Safanda, J.F.3
  • 8
    • 0028857169 scopus 로고
    • Normal phenotype in two brothers with a full FMR1 mutation
    • Smeets HJ, Smits AP, Verheij CE et al: Normal phenotype in two brothers with a full FMR1 mutation. Hum Mol Genet 1995; 4: 2103-2108.
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 2103-2108
    • Smeets, H.J.1    Smits, A.P.2    Verheij, C.E.3
  • 9
    • 0031985868 scopus 로고    scopus 로고
    • In vitro reactivation of the FMR1 gene involved in fragile X syndrome
    • Chiurazzi P, Pomponi MG, Willemsen R et al: In vitro reactivation of the FMR1 gene involved in fragile X syndrome. Hum Mol Genet 1998; 7: 109-113.
    • (1998) Hum. Mol. Genet. , vol.7 , pp. 109-113
    • Chiurazzi, P.1    Pomponi, M.G.2    Willemsen, R.3
  • 10
    • 0037100616 scopus 로고    scopus 로고
    • Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine
    • Pietrobono R, Pomponi MG, Tabolacci E et al: Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine. Nucleic Acids Res 2002; 30: 3278-3285.
    • (2002) Nucleic Acids Res. , vol.30 , pp. 3278-3285
    • Pietrobono, R.1    Pomponi, M.G.2    Tabolacci, E.3
  • 11
    • 0031837109 scopus 로고    scopus 로고
    • Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription
    • Jones PL, Veenstra GJC, Wade PA et al: Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription. Nat Genet 1998; 19: 187-191.
    • (1998) Nat. Genet. , vol.19 , pp. 187-191
    • Jones, P.L.1    Veenstra, G.J.C.2    Wade, P.A.3
  • 12
    • 0032574977 scopus 로고    scopus 로고
    • Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex
    • Nan X, Ng H-H, Johnson CA et al: Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex. Nature 1998; 393: 386-389.
    • (1998) Nature , vol.393 , pp. 386-389
    • Nan, X.1    Ng, H.-H.2    Johnson, C.A.3
  • 13
    • 0032168678 scopus 로고    scopus 로고
    • CpG methylation, chromatin structure and gene silencing - A three-way connection
    • Razin A: CpG methylation, chromatin structure and gene silencing - a three-way connection. EMBO J 1998; 17: 4905-4908.
    • (1998) EMBO J. , vol.17 , pp. 4905-4908
    • Razin, A.1
  • 14
    • 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 et al: Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells. Nat Genet 1999; 22: 98-101.
    • (1999) Nat. Genet. , vol.22 , pp. 98-101
    • Coffee, B.1    Zhang, F.2    Warren, S.T.3
  • 15
    • 0032741429 scopus 로고    scopus 로고
    • Synergistic effect of histone hyperacetylation and DNA demethylation in the reactivation of the FMR1 gene
    • Chiurazzi P, Pomponi MG, Pietrobono R et al: Synergistic effect of histone hyperacetylation and DNA demethylation in the reactivation of the FMR1 gene. Hum Mol Genet 1999; 8: 2317-2323.
    • (1999) Hum. Mol. Genet. , vol.8 , pp. 2317-2323
    • Chiurazzi, P.1    Pomponi, M.G.2    Pietrobono, R.3
  • 16
    • 0036850325 scopus 로고    scopus 로고
    • Cellular memory and the histone code
    • Turner BM: Cellular memory and the histone code. Cell 2002; 111: 285-291.
    • (2002) Cell , vol.111 , pp. 285-291
    • Turner, B.M.1
  • 17
    • 0042528729 scopus 로고    scopus 로고
    • Heterochromatin and epigenetic control of gene expression
    • Grewal SIS, Moazed D: Heterochromatin and epigenetic control of gene expression. Science 2003; 301: 798-802.
    • (2003) Science , vol.301 , pp. 798-802
    • Grewal, S.I.S.1    Moazed, D.2
  • 18
    • 0037672689 scopus 로고    scopus 로고
    • An epigenetic road map for histone lysine methylation
    • Lachner M, O'Sullivan RJ, Jenuwein T: An epigenetic road map for histone lysine methylation. J Cell Sci 2003; 116: 2117-2124.
    • (2003) J. Cell Sci. , vol.116 , pp. 2117-2124
    • Lachner, M.1    O'Sullivan, R.J.2    Jenuwein, T.3
  • 19
    • 0036782129 scopus 로고    scopus 로고
    • Histone modifications depict an aberrantly heterochromatinized FMR1 gene in fragile X syndrome
    • Coffee B, Zhang F, Ceman S et al: Histone modifications depict an aberrantly heterochromatinized FMR1 gene in fragile X syndrome. Am J Hum Genet 2002; 71: 923-932.
    • (2002) Am. J. Hum. Genet. , vol.71 , pp. 923-932
    • Coffee, B.1    Zhang, F.2    Ceman, S.3
  • 20
    • 0028244685 scopus 로고
    • Butyrate and acetyl-carnitine inhibit the cytogenetic expression of the fragile X in vitro
    • Pomponi MG, Neri G: Butyrate and acetyl-carnitine inhibit the cytogenetic expression of the fragile X in vitro. Am J Med Genet 1994; 51: 447-450.
    • (1994) Am. J. Med. Genet. , vol.51 , pp. 447-450
    • Pomponi, M.G.1    Neri, G.2
  • 21
    • 0033940157 scopus 로고    scopus 로고
    • Elevated levels of FMR1 mRNA in carrier males: A new mechanism of involvement in the fragile-X syndrome
    • Tassone F, Hagerman RJ, Taylor AK et al: Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome. Am J Hum Genet 2000; 66: 6-15.
    • (2000) Am. J. Hum. Genet. , vol.66 , pp. 6-15
    • Tassone, F.1    Hagerman, R.J.2    Taylor, A.K.3
  • 22
    • 0035964869 scopus 로고    scopus 로고
    • Correlation between histone lysine methylation and developmental changes at the chicken beta-globin locus
    • Litt MD, Simpson M, Gaszner M et al: Correlation between histone lysine methylation and developmental changes at the chicken beta-globin locus. Science 2001; 293: 2453-2455.
    • (2001) Science , vol.293 , pp. 2453-2455
    • Litt, M.D.1    Simpson, M.2    Gaszner, M.3
  • 23
    • 0032748826 scopus 로고    scopus 로고
    • Double-blind, placebo-controlled study of L-acetylcarnitine for the treatment of hyperactive behavior in fragile X syndrome
    • Torrioli MG, Vernacotola S, Mariotti P et al: Double-blind, placebo-controlled study of L-acetylcarnitine for the treatment of hyperactive behavior in fragile X syndrome. Am J Med Genet 1999; 87: 366-368.
    • (1999) Am. J. Med. Genet. , vol.87 , pp. 366-368
    • Torrioli, M.G.1    Vernacotola, S.2    Mariotti, P.3
  • 24
    • 0037805263 scopus 로고    scopus 로고
    • Modulation of methylation in the FMR1 promoter region after long term treatment with L-carnitine and acetyl-L-carnitine
    • Pascale E, Battiloro E, Reale GC et al: Modulation of methylation in the FMR1 promoter region after long term treatment with L-carnitine and acetyl-L-carnitine. J Med Genet 2003; 40: e76.
    • (2003) J. Med. Genet. , vol.40
    • Pascale, E.1    Battiloro, E.2    Reale, G.C.3
  • 25
    • 0348150714 scopus 로고    scopus 로고
    • Maintenance of stable heterochromatin domains by dynamic HP1 binding
    • Cheutin T, McNairn AJ, Jenuwein T et al: Maintenance of stable heterochromatin domains by dynamic HP1 binding. Science 2003; 299: 721-725.
    • (2003) Science , vol.299 , pp. 721-725
    • Cheutin, T.1    McNairn, A.J.2    Jenuwein, T.3
  • 26
    • 0036532202 scopus 로고    scopus 로고
    • Histone methylation in transcriptional control
    • Kouzarides T: Histone methylation in transcriptional control. Curr Opin Genet Dev 2002; 12: 198-209.
    • (2002) Curr. Opin. Genet. Dev. , vol.12 , pp. 198-209
    • Kouzarides, T.1
  • 27
    • 19944431036 scopus 로고    scopus 로고
    • Molecular dissection of the events leading to inactivation of the FMR1 gene
    • Pietrobono, R, Tabolacci E, Zalfa F et al: Molecular dissection of the events leading to inactivation of the FMR1 gene. Hum Mol Genet 2005; 14: 267-277.
    • (2005) Hum. Mol. Genet. , vol.14 , pp. 267-277
    • Pietrobono, R.1    Tabolacci, E.2    Zalfa, F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.