Genomic imprinting: Parental influence on the genome

被引:1686
作者
Reik, W [1 ]
Walter, J
机构
[1] Babraham Inst, Lab Dev Genet & Imprinting, Dev Genet Programme, Cambridge CB2 4AT, England
[2] Max Planck Inst Mol Genet, D-14195 Berlin, Germany
[3] Univ Saarland, D-66041 Saarbrucken, Germany
关键词
D O I
10.1038/35047554
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genomic imprinting affects several dozen mammalian genes and results in the expression of those genes from only one of the two parental chromosomes. This is brought about by epigenetic instructions - imprints - that are laid down in the parental germ cells. Imprinting is a particularly important genetic mechanism in mammals, and is thought to influence the transfer of nutrients to the fetus and the newborn from the mother. Consistent with this view is the fact that imprinted genes tend to affect growth in the womb and behaviour after birth. Aberrant imprinting disturbs development and is the cause of various disease syndromes. The study of imprinting also provides new insights into epigenetic gene modification during development.
引用
收藏
页码:21 / 32
页数:12
相关论文
共 118 条
  • [1] Ainscough JFX, 2000, DEVELOPMENT, V127, P3923
  • [2] THE MOUSE INSULIN-LIKE GROWTH-FACTOR TYPE-2 RECEPTOR IS IMPRINTED AND CLOSELY LINKED TO THE TME LOCUS
    BARLOW, DP
    STOGER, R
    HERRMANN, BG
    SAITO, K
    SCHWEIFER, N
    [J]. NATURE, 1991, 349 (6304) : 84 - 87
  • [3] PARENTAL IMPRINTING OF THE MOUSE H19 GENE
    BARTOLOMEI, MS
    ZEMEL, S
    TILGHMAN, SM
    [J]. NATURE, 1991, 351 (6322) : 153 - 155
  • [4] EPIGENETIC MECHANISMS UNDERLYING THE IMPRINTING OF THE MOUSE H19-GENE
    BARTOLOMEI, MS
    WEBBER, AL
    BRUNKOW, ME
    TILGHMAN, SM
    [J]. GENES & DEVELOPMENT, 1993, 7 (09) : 1663 - 1673
  • [5] Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene
    Bell, AC
    Felsenfeld, G
    [J]. NATURE, 2000, 405 (6785) : 482 - 485
  • [6] De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch
    Bielinska, B
    Blaydes, SM
    Buiting, K
    Yang, T
    Krajewska-Walasek, M
    Horsthemke, B
    Brannan, CI
    [J]. NATURE GENETICS, 2000, 25 (01) : 74 - 78
  • [7] Methylation-induced repression - Belts, braces, and chromatin
    Bird, AP
    Wolffe, AP
    [J]. CELL, 1999, 99 (05) : 451 - 454
  • [8] Abnormal methylation does not prevent X inactivation in ICF patients
    Bourc'his, D
    Miniou, P
    Jeanpierre, M
    Gomes, DM
    Dupont, JM
    De Saint-Basile, G
    Maraschio, P
    Tiepolo, L
    Viegas-Péquignot, E
    [J]. CYTOGENETICS AND CELL GENETICS, 1999, 84 (3-4): : 245 - 252
  • [9] A role for the Ras signalling pathway in synaptic transmission and long-term memory
    Brambilla, R
    Gnesutta, N
    Minichiello, L
    White, G
    Roylance, AJ
    Herron, CE
    Ramsey, M
    Wolfer, DP
    Cestari, V
    RossiArnaud, C
    Grant, SGN
    Chapman, PF
    Lipp, HP
    Sturani, E
    Klein, R
    [J]. NATURE, 1997, 390 (6657) : 281 - 286
  • [10] THE ONTOGENY OF ALLELE-SPECIFIC METHYLATION ASSOCIATED WITH IMPRINTED GENES IN THE MOUSE
    BRANDEIS, M
    KAFRI, T
    ARIEL, M
    CHAILLET, JR
    MCCARREY, J
    RAZIN, A
    CEDAR, H
    [J]. EMBO JOURNAL, 1993, 12 (09) : 3669 - 3677