Imprinting regulation of the murine Meg1/Grb10 and human GRB10 genes;: roles of brain-specific promoters and mouse-specific CTCF-binding sites

被引:90
作者
Hikichi, T
Kohda, T
Kaneko-Ishino, T
Ishino, F
机构
[1] Tokyo Inst Technol, Ctr Gene Res, Midori Ku, Yokohama, Kanagawa 2268501, Japan
[2] Japan Sci & Technol Corp, CREST, Kawaguchi, Saitama 3320012, Japan
[3] Tokai Univ, Sch Hlth Sci, Kanagawa 2591193, Japan
关键词
D O I
10.1093/nar/gkg232
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The imprinted mouse gene Meg1/Grb10 is expres sed from maternal alleles in almost all tissues and organs, except in the brain, where it is expressed biallelically, and the paternal allele is expressed preferentially in adulthood. In contrast, the human GRB10 gene shows equal biallelic expression in almost all tissues and organs, while it is almost always expressed paternally in the fetal brain. To elucidate the molecular mechanisms of the complex imprinting patterns among the different tissues and organs of humans and mice, we analyzed in detail both the genomic structures and tissue-specific expression profiles of these species. Experiments using 5'-RACE and RT-PCR demonstrated the existence in both humans and mice of novel brain- specific promoters, in which only the paternal allele was active. The promoters were located in the primary differentially methylated regions. Interest ingly, CTCF-binding sites were found only in the mouse promoter region where CTCF showed DNA methylation-sensitive binding activity. Thus, the insulator function of CTCF might cause reciprocal maternal expression of the Meg1/Grb10 gene from another upstream promoter in the mouse, whereas the human upstream promoter is active in both parental alleles due to the lack of the corresponding insulator sequence in this region.
引用
收藏
页码:1398 / 1406
页数:9
相关论文
共 37 条
  • [1] The SH2-containing adapter protein GRB10 interacts with BCR-ABL
    Bai, RY
    Jahn, T
    Schrem, S
    Munzert, G
    Weidner, KM
    Wang, JYJ
    Duyster, J
    [J]. ONCOGENE, 1998, 17 (08) : 941 - 948
  • [2] Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene
    Bell, AC
    Felsenfeld, G
    [J]. NATURE, 2000, 405 (6785) : 482 - 485
  • [3] Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion
    Blagitko, N
    Mergenthaler, S
    Schulz, U
    Wollmann, HA
    Craigen, W
    Eggermann, T
    Ropers, HH
    Kalscheuer, VM
    [J]. HUMAN MOLECULAR GENETICS, 2000, 9 (11) : 1587 - 1595
  • [4] Two imprinted gene mutations: three phenotypes
    Cattanach, BM
    Peters, J
    Ball, S
    Rasberry, C
    [J]. HUMAN MOLECULAR GENETICS, 2000, 9 (15) : 2263 - 2273
  • [5] Association of a redefined proximal mouse chromosome 11 imprinting region and U2afbp-rs/U2af1-rs1 expression
    Cattanach, BM
    Shibata, H
    Hayashizaki, Y
    Townsend, KMS
    Ball, S
    Beechey, CV
    [J]. CYTOGENETICS AND CELL GENETICS, 1998, 80 (1-4): : 41 - 47
  • [6] PARENTAL IMPRINTING OF THE MOUSE INSULIN-LIKE GROWTH FACTOR-II GENE
    DECHIARA, TM
    ROBERTSON, EJ
    EFSTRATIADIS, A
    [J]. CELL, 1991, 64 (04) : 849 - 859
  • [7] CHROMATIN STRUCTURE AND IMPRINTING - DEVELOPMENTAL CONTROL OF DNASE-I SENSITIVITY IN THE MOUSE INSULIN-LIKE-GROWTH-FACTOR-2 GENE
    FEIL, R
    HANDEL, MA
    ALLEN, ND
    REIK, W
    [J]. DEVELOPMENTAL GENETICS, 1995, 17 (03): : 240 - 252
  • [8] CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus
    Hark, AT
    Schoenherr, CJ
    Katz, DJ
    Ingram, RS
    Levorse, JM
    Tilghman, SM
    [J]. NATURE, 2000, 405 (6785) : 486 - 489
  • [9] DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressed
    Hitchins, MP
    Bentley, L
    Monk, D
    Beechey, C
    Peters, J
    Kelsey, G
    Ishino, F
    Preece, MA
    Stanier, P
    Moore, GE
    [J]. MAMMALIAN GENOME, 2002, 13 (12) : 686 - 691
  • [10] Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB70 in Silver-Russell syndrome
    Hitchins, MP
    Monk, D
    Bell, GM
    Ali, Z
    Preece, MA
    Stanier, P
    Moore, GE
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2001, 9 (02) : 82 - 90