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Volumn 3, Issue 5, 2014, Pages 699-706

FMR1 epigenetic silencing commonly occurs in undifferentiated fragile X-affected embryonic stem cells

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR CTCF; 5' UNTRANSLATED REGION; FMR1 PROTEIN, HUMAN; FRAGILE X MENTAL RETARDATION PROTEIN; HISTONE; LYSINE; OCTAMER TRANSCRIPTION FACTOR 4; POU5F1 PROTEIN, HUMAN; SOX2 PROTEIN, HUMAN; TRANSCRIPTION FACTOR SOX;

EID: 84922571389     PISSN: 22136711     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.stemcr.2014.09.001     Document Type: Article
Times cited : (61)

References (29)
  • 2
    • 0032905253 scopus 로고    scopus 로고
    • Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells
    • Coffee, B., Zhang, F., Warren, S.T., and 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
  • 3
    • 0036782129 scopus 로고    scopus 로고
    • Histone modifications depict an aberrantly heterochromatinized FMR1 gene in fragile x syndrome
    • Coffee, B., Zhang, F., Ceman, S., Warren, S.T., and Reines, D. (2002). Histone modifications depict an aberrantly heterochromatinized FMR1 gene in fragile x syndrome. Am. J. Hum. Genet. 71, 923-932.
    • (2002) Am. J. Hum. Genet. , vol.71 , pp. 923-932
    • Coffee, B.1    Zhang, F.2    Ceman, S.3    Warren, S.T.4    Reines, D.5
  • 5
    • 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., Boué, J., Mandel, J.L., and Oberlé, 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    Boué, J.4    Mandel, J.L.5    Oberlé, I.6
  • 10
    • 78149272981 scopus 로고    scopus 로고
    • The distribution of repressive histone modifications on silenced FMR1 alleles provides clues to the mechanism of gene silencing in fragile X syndrome
    • Kumari, D., and Usdin, K. (2010). The distribution of repressive histone modifications on silenced FMR1 alleles provides clues to the mechanism of gene silencing in fragile X syndrome. Hum. Mol. Genet. 19, 4634-4642.
    • (2010) Hum. Mol. Genet. , vol.19 , pp. 4634-4642
    • Kumari, D.1    Usdin, K.2
  • 17
    • 84856879093 scopus 로고    scopus 로고
    • Molecular mechanisms of fragile X syndrome: A twenty-year perspective
    • Santoro, M.R., Bray, S.M., and Warren, S.T. (2012). Molecular mechanisms of fragile X syndrome: a twenty-year perspective. Annu. Rev. Pathol. 7, 219-245.
    • (2012) Annu. Rev. Pathol. , vol.7 , pp. 219-245
    • Santoro, M.R.1    Bray, S.M.2    Warren, S.T.3
  • 18
    • 42449163490 scopus 로고    scopus 로고
    • X-inactivation in female human embryonic stem cells is in a nonrandompattern and prone to epigenetic alterations
    • Shen, Y., Matsuno, Y., Fouse, S.D., Rao, N., Root, S., Xu, R., Pellegrini, M., Riggs, A.D., and Fan, G. (2008). X-inactivation in female human embryonic stem cells is in a nonrandompattern and prone to epigenetic alterations. Proc. Natl. Acad. Sci. USA 105, 4709-4714.
    • (2008) Proc. Natl. Acad. Sci. USA , vol.105 , pp. 4709-4714
    • Shen, Y.1    Matsuno, Y.2    Fouse, S.D.3    Rao, N.4    Root, S.5    Xu, R.6    Pellegrini, M.7    Riggs, A.D.8    Fan, G.9
  • 19
    • 80053948646 scopus 로고    scopus 로고
    • Epigenetic characterization of the FMR1 gene and aberrant neurodevelopment in human induced pluripotent stem cell models of fragile X syndrome
    • Sheridan, S.D., Theriault, K.M., Reis, S.A., Zhou, F., Madison, J.M., Daheron, L., Loring, J.F., and Haggarty, S.J. (2011). Epigenetic characterization of the FMR1 gene and aberrant neurodevelopment in human induced pluripotent stem cell models of fragile X syndrome. PLoS ONE 6, e26203.
    • (2011) PLoS ONE , vol.6 , pp. e26203
    • Sheridan, S.D.1    Theriault, K.M.2    Reis, S.A.3    Zhou, F.4    Madison, J.M.5    Daheron, L.6    Loring, J.F.7    Haggarty, S.J.8
  • 22
    • 0027327326 scopus 로고
    • Prenatal diagnosis of a hypermethylated full fragile X mutation in chorionic villi of a male fetus
    • Suzumori, K., Yamauchi, M., Seki, N., Kondo, I., and Hori, T. (1993). Prenatal diagnosis of a hypermethylated full fragile X mutation in chorionic villi of a male fetus. J. Med. Genet. 30, 785-787.
    • (1993) J. Med. Genet. , vol.30 , pp. 785-787
    • Suzumori, K.1    Yamauchi, M.2    Seki, N.3    Kondo, I.4    Hori, T.5
  • 23
    • 18844398832 scopus 로고    scopus 로고
    • Differential epigenetic modifications in the FMR1 gene of the fragile X syndrome after reactivating pharmacological treatments
    • Tabolacci, E., Pietrobono, R., Moscato, U., Oostra, B.A., Chiurazzi, P., and Neri, G. (2005). Differential epigenetic modifications in the FMR1 gene of the fragile X syndrome after reactivating pharmacological treatments. Eur. J. Hum. Genet. 13, 641-648.
    • (2005) Eur. J. Hum. Genet. , vol.13 , pp. 641-648
    • Tabolacci, E.1    Pietrobono, R.2    Moscato, U.3    Oostra, B.A.4    Chiurazzi, P.5    Neri, G.6
  • 24
    • 56749106679 scopus 로고    scopus 로고
    • Epigenetic analysis reveals a euchromatic configuration in the FMR1 unmethylated full mutations
    • Tabolacci, E., Moscato, U., Zalfa, F., Bagni, C., Chiurazzi, P., and Neri, G. (2008). Epigenetic analysis reveals a euchromatic configuration in the FMR1 unmethylated full mutations. Eur. J. Hum. Genet. 16, 1487-1498.
    • (2008) Eur. J. Hum. Genet. , vol.16 , pp. 1487-1498
    • Tabolacci, E.1    Moscato, U.2    Zalfa, F.3    Bagni, C.4    Chiurazzi, P.5    Neri, G.6
  • 25
    • 0034945678 scopus 로고    scopus 로고
    • A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA
    • Tassone, F., Hagerman, R.J., Taylor, A.K., and Hagerman, P.J. (2001). A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA. J. Med. Genet. 38, 453-456.
    • (2001) J. Med. Genet. , vol.38 , pp. 453-456
    • Tassone, F.1    Hagerman, R.J.2    Taylor, A.K.3    Hagerman, P.J.4
  • 26
    • 84872370488 scopus 로고    scopus 로고
    • Neural differentiation of Fragile X human Embryonic Stem Cells reveals abnormal patterns of development despite successful neurogenesis
    • Telias, M., Segal, M., and Ben-Yosef, D. (2013). Neural differentiation of Fragile X human Embryonic Stem Cells reveals abnormal patterns of development despite successful neurogenesis. Dev. Biol. 374, 32-45.
    • (2013) Dev. Biol. , vol.374 , pp. 32-45
    • Telias, M.1    Segal, M.2    Ben-Yosef, D.3
  • 27
    • 77956214743 scopus 로고    scopus 로고
    • Differential modeling of fragile X syndrome by human embryonic stem cells and induced pluripotent stem cells
    • Urbach, A., Bar-Nur, O., Daley, G.Q., and Benvenisty, N. (2010). Differential modeling of fragile X syndrome by human embryonic stem cells and induced pluripotent stem cells. Cell Stem Cell 6, 407-411.
    • (2010) Cell Stem Cell , vol.6 , pp. 407-411
    • Urbach, A.1    Bar-Nur, O.2    Daley, G.Q.3    Benvenisty, N.4
  • 28
    • 0025905795 scopus 로고
    • Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
    • Verkerk, A.J., Pieretti, M., Sutcliffe, J.S., Fu, Y.H., Kuhl, D.P., Pizzuti, A., Reiner, O., Richards, S., Victoria, M.F., Zhang, F.P., et al. (1991). Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell 65, 905-914.
    • (1991) Cell , vol.65 , pp. 905-914
    • Verkerk, A.J.1    Pieretti, M.2    Sutcliffe, J.S.3    Fu, Y.H.4    Kuhl, D.P.5    Pizzuti, A.6    Reiner, O.7    Richards, S.8    Victoria, M.F.9    Zhang, F.P.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.