Nucleosome positioning signals in the DNA sequence of the human and mouse H19 imprinting control regions

被引:16
作者
Davey, C
Fraser, R
Smolle, M
Simmen, MW
Allan, J
机构
[1] Univ Edinburgh, Inst Cell & Mol Biol, Edinburgh EH9 3JR, Midlothian, Scotland
[2] Univ Edinburgh, Dept Biomed Sci, Edinburgh EH8 9XD, Midlothian, Scotland
基金
英国惠康基金;
关键词
chromatin; nucleosome; H19; imprinting; CpG methylation;
D O I
10.1016/S0022-2836(02)01340-2
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
We have investigated the sequences of the mouse and human H19 imprinting control regions (ICRs) to see whether they contain nucleosome positioning information pertinent to their function as a methylation-regulated chromatin boundary. Positioning signals were identified by an in vitro approach that employs reconstituted chromatin to comprehensively describe the contribution of the DNA to the most basic, underlying level of chromatin structure. Signals in the DNA sequence of both ICRs directed nucleosomes to flank and encompass the short conserved sequences that constitute the binding sites for the zinc finger protein CTCF, an essential mediator of insulator activity. The repeat structure of the human ICR presented a conserved array of strong positioning signals that would preferentially flank these CTCF binding sites with positioned nucleosomes, a chromatin structure that would tend to maintain their accessibility. Conversely, all four CTCF binding sites in the mouse sequence were located close to the centre of positioning signals that were stronger than those in their flanks; these binding sites might therefore be expected to be more readily incorporated into positioned nucleosomes. We found that CpG methylation did not effect widespread repositioning of nucleosomes on either ICR, indicating that allelic methylation patterns were unlikely to establish allele-specific chromatin structures for H19 by operating directly upon the underlying DNA-histone interactions; instead, epigenetic modulation of ICR chromatin structure is likely to be mediated principally at higher levels of control. DNA methylation did, however, both promote and inhibit nucleosome positioning at several sites in both ICRs and substantially negated one of the strongest nucleosome positioning signals in the human sequence, observations that underline the fact that this epigenetic modification can, nevertheless, directly and decisively modulate core histone-DNA interactions within the nucleosome. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:873 / 887
页数:15
相关论文
共 41 条
  • [1] The protein CTCF is required for the enhancer blocking activity of vertebrate insulators
    Bell, AC
    West, AG
    Felsenfeld, G
    [J]. CELL, 1999, 98 (03) : 387 - 396
  • [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] The exocyclic groups of DNA modulate the affinity and positioning of the histone octamer
    Buttinelli, M
    Minnock, A
    Panetta, G
    Waring, M
    Travers, A
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (15) : 8544 - 8549
  • [4] PERIODICITY OF STRONG NUCLEOSOME POSITIONING SITES AROUND THE CHICKEN ADULT BETA-GLOBIN GENE MAY ENCODE REGULARLY SPACED CHROMATIN
    DAVEY, C
    PENNINGS, S
    MEERSSEMAN, G
    WESS, TJ
    ALLAN, J
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (24) : 11210 - 11214
  • [5] CpG methylation remodels chromatin structure in vitro
    Davey, C
    Pennings, S
    Allan, J
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1997, 267 (02) : 276 - 288
  • [6] DAVEY C, 1998, CHROMATIN PRACTICAL, P153
  • [7] Parental chromosome-specific chromatin conformation in the imprinted U2af1-rs1 gene in the mouse
    Feil, R
    Boyano, MD
    Allen, ND
    Kelsey, G
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (33) : 20893 - 20900
  • [8] Methylation sequencing analysis refines the region of H19 epimutation in Wilms tumor
    Frevel, MAE
    Sowerby, SJ
    Petersen, GB
    Reeve, AE
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (41) : 29331 - 29340
  • [9] A potential imprint control element -: identification of a conserved 42 bp sequence upstream of H19
    Frevel, MAE
    Hornberg, JJ
    Reeve, AE
    [J]. TRENDS IN GENETICS, 1999, 15 (06) : 216 - 218
  • [10] Relationship between DNA methylation, histone H4 acetylation and gene expression in the mouse imprinted Igf2-H19 domain
    Grandjean, V
    O'Neill, L
    Sado, T
    Turner, B
    Ferguson-Smith, A
    [J]. FEBS LETTERS, 2001, 488 (03) : 165 - 169