Mammalian Genomic Imprinting

被引:329
作者
Bartolomei, Marisa S. [1 ]
Ferguson-Smith, Anne C. [2 ]
机构
[1] Univ Penn, Sch Med, Dept Cell & Dev Biol, Philadelphia, PA 19063 USA
[2] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge, England
来源
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY | 2011年 / 3卷 / 07期
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
BECKWITH-WIEDEMANN-SYNDROME; MOUSE H19 GENE; DNA METHYLATION; PRADER-WILLI; GERM-CELLS; PREIMPLANTATION DEVELOPMENT; PATERNAL METHYLATION; GROWTH-RETARDATION; MATERNAL-BEHAVIOR; PARENTAL ORIGIN;
D O I
10.1101/cshperspect.a002592
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Normal mammalian development requires a maternal and paternal contribution, which is attributed to imprinted genes, or genes that are expressed from a single parental allele. Approximately 100 imprinted genes have been reported in mammals thus far. Imprinted genes are controlled by cis-acting regulatory elements, termed imprinting control regions (ICRs), which have parental-specific epigenetic modifications, including DNA methylation. ICRs are methylated by de novo DNA methyltransferases during germline development; these parental-specific modifications must be maintained following fertilization when the genome is extensively reprogrammed. Many imprinted genes reside in similar to 1-megabase clusters, with two major mechanisms of imprinting regulation currently recognized, CTCF-dependent insulators and long noncoding RNAs. Unclustered imprinted genes are generally regulated by germline-derived differential promoter methylation. Here, we describe the identification and functions of imprinted genes, cis-acting control sequences, trans-acting factors, and imprinting mechanisms in clusters. Finally, we define questions that require more extensive research.
引用
收藏
页码:1 / 17
页数:17
相关论文
共 101 条
  • [1] Conserved interaction between distinct Kruppel-associated box domains and the transcriptional intermediary factor 1 β
    Abrink, M
    Ortiz, JA
    Mark, C
    Sanchez, C
    Looman, C
    Hellman, L
    Chambon, P
    Losson, R
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (04) : 1422 - 1426
  • [2] The genetic aetiology of Silver-Russell syndrome
    Abu-Amero, S.
    Monk, D.
    Frost, J.
    Preece, M.
    Stanier, P.
    Moore, G. E.
    [J]. JOURNAL OF MEDICAL GENETICS, 2008, 45 (04) : 193 - 199
  • [3] Global Survey of Genomic Imprinting by Transcriptome Sequencing
    Babak, Tomas
    DeVeale, Brian
    Armour, Christopher
    Raymond, Christopher
    Cleary, Michele A.
    van der Kooy, Derek
    Johnson, Jason M.
    Lim, Lee P.
    [J]. CURRENT BIOLOGY, 2008, 18 (22) : 1735 - 1741
  • [4] 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
  • [5] PARENTAL IMPRINTING OF THE MOUSE H19 GENE
    BARTOLOMEI, MS
    ZEMEL, S
    TILGHMAN, SM
    [J]. NATURE, 1991, 351 (6322) : 153 - 155
  • [6] Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene
    Bell, AC
    Felsenfeld, G
    [J]. NATURE, 2000, 405 (6785) : 482 - 485
  • [7] DNA methylation patterns and epigenetic memory
    Bird, A
    [J]. GENES & DEVELOPMENT, 2002, 16 (01) : 6 - 21
  • [8] Dnmt3L and the establishment of maternal genomic imprints
    Bourc'his, D
    Xu, GL
    Lin, CS
    Bollman, B
    Bestor, TH
    [J]. SCIENCE, 2001, 294 (5551) : 2536 - 2539
  • [9] Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L
    Bourc'his, D
    Bestor, TH
    [J]. NATURE, 2004, 431 (7004) : 96 - 99
  • [10] CATTANACH BM, 1986, J EMBRYOL EXP MORPH, V97, P137