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Volumn 195, Issue 1, 2001, Pages 97-110

DNA methylation in genomic imprinting, development, and disease

Author keywords

Angelman syndrome; Beckwith Wiedemann syndrome; Cancer; Imprinting; Methylation; Prader Willi syndrome

Indexed keywords

ALLELE; BECKWITH WIEDEMANN SYNDROME; CANCER; CHROMATIN STRUCTURE; CONTROLLED STUDY; DEVELOPMENT; DNA METHYLATION; GENE CONTROL; GENE EXPRESSION REGULATION; GENE SILENCING; GENOME IMPRINTING; HAPPY PUPPET SYNDROME; HUMAN; MOUSE; NONHUMAN; PHYSICAL DISEASE; PRADER WILLI SYNDROME; PRIORITY JOURNAL; REVIEW; TISSUE DIFFERENTIATION; X CHROMOSOME INACTIVATION;

EID: 0034801809     PISSN: 00223417     EISSN: None     Source Type: Journal    
DOI: 10.1002/path.890     Document Type: Review
Times cited : (227)

References (130)
  • 2
    • 0031860739 scopus 로고    scopus 로고
    • Cloning and characterization of a family of novel mammalian DNA (cytosine-5) methyltransferases
    • (1998) Nature Genet , vol.19 , pp. 219-220
    • Okano, M.1    Xie, S.2    Li, E.3
  • 24
    • 0034098812 scopus 로고    scopus 로고
    • Mechanisms leading to uniparental disomy and their clinical consequences
    • (2000) Bioessays , vol.22 , pp. 452-459
    • Robinson, W.P.1
  • 36
    • 0023119242 scopus 로고
    • Temporal and regional changes in DNA methylation in the embryonic, extraembryonic and germ cell lineages during mouse embryo development
    • (1987) Development , vol.99 , pp. 371-382
    • Monk, M.1    Boubelik, M.2    Lehnert, S.3
  • 43
  • 46
    • 0029935327 scopus 로고    scopus 로고
    • Germ-line passage is required for establishment of methylation and expression patterns of imprinted but not of nonimprinted genes
    • (1996) Genes Dev , vol.10 , pp. 1008-1020
    • Tucker, K.L.1    Beard, C.2    Dausmann, J.3
  • 47
    • 0029142492 scopus 로고
    • Biallelic expression of imprinted genes in the mouse germ line: Implications for erasure, establishment, and mechanisms of genomic imprinting
    • (1995) Genes Dev , vol.9 , pp. 1857-1868
    • Szabo, P.E.1    Mann, J.R.2
  • 57
    • 0033609117 scopus 로고    scopus 로고
    • Loss of imprinting of a paternally expressed transcript, with antisense orientation to KvLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting
    • (1999) Proc Natl Acad Sci U S A , vol.96 , pp. 5203-5208
    • Lee, M.P.1    DeBaun, M.R.2    Mitsuya, K.3
  • 58
    • 0032813924 scopus 로고    scopus 로고
    • LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids
    • (1999) Hum Mol Genet , vol.8 , pp. 1209-1217
    • Mitsuya, K.1    Meguro, M.2    Lee, M.P.3
  • 67
    • 0031870673 scopus 로고    scopus 로고
    • Regulation of the Wilms' tumour suppressor (WT1) gene by an antisense RNA: A link with genomic imprinting?
    • (1998) J Pathol , vol.185 , pp. 342-344
    • Ward, A.1    Dutton, J.R.2
  • 70
    • 0034713375 scopus 로고    scopus 로고
    • Methylation of a CTCF-dependent boundary control imprinted expression of the Igf2 gene
    • (2000) Nature , vol.405 , pp. 482-485
    • Bell, A.C.1    Felsenfeld, G.2
  • 74
    • 0028954144 scopus 로고
    • Methylation at CpG sequences does not influence histone H1 binding to a nucleosome including a Xenopus borealis 5 S rRNA gene
    • (1995) J Bio Chem , vol.270 , pp. 4197-4200
    • Nightingale, K.1    Wolffe, A.P.2
  • 76
    • 0034659231 scopus 로고    scopus 로고
    • De novo nucleosome assembly: New pieces in an old puzzle
    • (2000) Genes Dev , vol.14 , pp. 1430-1438
    • Verreault, A.1
  • 80
  • 86
    • 0031964299 scopus 로고    scopus 로고
    • The paternal allele of the H19 gene is progressively silenced during early mouse development: The acetylation status of histones may be involved in the generation of variegated expression patterns
    • (1998) Development , vol.125 , pp. 61-69
    • Svensson, K.1    Mattsson, R.2    James, T.C.3
  • 88
    • 0033924890 scopus 로고    scopus 로고
    • Parent-of-origin specific histone acetylation and reactivation of a key imprinted gene locus in Prader-Willi syndrome
    • (2000) Am J Hum Genet , vol.66 , pp. 1958-1962
    • Saitoh, S.1    Wada, T.2
  • 101
    • 0033035048 scopus 로고    scopus 로고
    • In vivo nuclease hypersensitivity studies reveal multiple sites of parental origin-dependent differential chromatin conformation in the 150 kb SNRPN transcription unit
    • (1999) Hum Mol Genet , vol.8 , pp. 555-566
    • Schweizer, J.1    Zynger, D.2    Francke, U.3
  • 102
    • 0034284693 scopus 로고    scopus 로고
    • Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome
    • (2000) Hum Mol Genet , vol.9 , pp. 2075-2083
    • Horike, S.1    Mitsuya, K.2    Meguro, M.3
  • 124
    • 0034105545 scopus 로고    scopus 로고
    • DNA methylation inhibitors in the treatment of leukemias, myelodysplastic syndromes and hemoglobinpathies: Clinical results and possible mechanisms of action
    • (2000) Curr Top Microbiol Immunol , vol.249 , pp. 135-164
    • Luebbert, M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.