Genomic imprinting and chromatin insulation in Beckwith-Wiedemann syndrome

被引:4
作者
Greally, JM [1 ]
机构
[1] Yale Univ, Sch Med, Dept Genet, New Haven, CT 06520 USA
基金
美国国家卫生研究院;
关键词
genomic imprinting; Beckwith-Weidemann syndrome; chromatin; CpG islands; chromosome abnormalities; insulin-like growth factor II; heterochromatin;
D O I
10.1007/BF02915809
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
Genes are recognized as undergoing genomic imprinting when they are capable of being expressed only from the paternal or only from the maternal chromosome. The process can occur coordinately within large physical domains in mammalian chromosomes. One interesting facet of the study of genomic imprinting is that it offers insight into the regulation of large chromosomal regions. Understanding this regulation involves elucidating the cis-acting regulators of gene expression and defining the:elements that-maintain chromatin insulation, both required for understanding more practically applicable areas of biological research,: such as efficient transgene production. This review is focused on the regulation of the imprinted domain of human chromosome 11p15.5, responsible for Beckwith-Wiedemann syndrome (BWS). Recent findings indicate that the maintenance of imprinting within this domain is critically dependent on the stable maintenance of chromatin insulation.
引用
收藏
页码:159 / 173
页数:15
相关论文
共 128 条
  • [51] Biallelic expression of the H19 and IGF2 genes in hepatocellular carcinoma
    Kim, KS
    Lee, YI
    [J]. CANCER LETTERS, 1997, 119 (02) : 143 - 148
  • [52] Relaxation of imprinting of the insulin-like growth factor II gene in colorectal cancer
    Kinouchi, Y
    Hiwatashi, N
    Higashioka, S
    Nagashima, F
    Chida, M
    Toyota, T
    [J]. CANCER LETTERS, 1996, 107 (01) : 105 - 108
  • [53] ALLELE-SPECIFIC REPLICATION TIMING OF IMPRINTED GENE REGIONS
    KITSBERG, D
    SELIG, S
    BRANDEIS, M
    SIMON, I
    KESHET, I
    DRISCOLL, DJ
    NICHOLLS, RD
    CEDAR, H
    [J]. NATURE, 1993, 364 (6436) : 459 - 463
  • [54] TARGETED DISRUPTION OF THE TYROSINE-HYDROXYLASE LOCUS RESULTS IN SEVERE CATECHOLAMINE DEPLETION AND PERINATAL LETHALITY IN MICE
    KOBAYASHI, K
    MORITA, S
    SAWADA, H
    MIZUGUCHI, T
    YAMADA, K
    NAGATSU, I
    HATA, T
    WATANABE, Y
    FUJITA, K
    NAGATSU, T
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (45) : 27235 - 27243
  • [55] Scaffold-associated regions: cis-acting determinants of chromatin structural loops and functional domains
    Laemmli, Ulrich K.
    Kaes, Emmanuel
    Poljak, Leonora
    Adachi, Yasuhisa
    [J]. CURRENT OPINION IN GENETICS & DEVELOPMENT, 1992, 2 (02) : 275 - 285
  • [56] Lee MP, 1998, CANCER RES, V58, P1052
  • [57] Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements
    Lee, MP
    Hu, RJ
    Johnson, LA
    Feinberg, AP
    [J]. NATURE GENETICS, 1997, 15 (02) : 181 - 185
  • [58] DISRUPTION OF IMPRINTING CAUSED BY DELETION OF THE H19 GENE REGION IN MICE
    LEIGHTON, PA
    INGRAM, RS
    EGGENSCHWILER, J
    EFSTRATIADIS, A
    TILGHMAN, SM
    [J]. NATURE, 1995, 375 (6526) : 34 - 39
  • [59] AN ENHANCER DELETION AFFECTS BOTH H19 AND IGF2 EXPRESSION
    LEIGHTON, PA
    SAAM, JR
    INGRAM, RS
    STEWART, CL
    TILGHMAN, SM
    [J]. GENES & DEVELOPMENT, 1995, 9 (17) : 2079 - 2089
  • [60] Li Madeline, 1997, Current Opinion in Pediatrics, V9, P623, DOI 10.1097/00008480-199712000-00012