Chromatin structural features and targets that regulate transcription

被引:274
作者
Wolffe, AP [1 ]
Guschin, D [1 ]
机构
[1] NICHHD, Mol Embryol Lab, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1006/jsbi.2000.4217
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 nucleosome and chromatin fiber provide the common structural framework for transcriptional control in eukaryotes. The folding of DNA within these structures can both promote and impede transcription dependent on structural context. Importantly, neither the nucleosome nor the chromatin fiber is a static structure. Histone dissociation, histone modification, nucleosome mobility, and assorted allosteric transitions contribute to transcriptional control. Chromatin remodeling is associated with gene activation and repression. Energy-dependent processes mediate the assembly of both activating and repressive proteins into the nucleosomal infrastructure. Recent progress allows the structural consequences of these processes to be visualized at the chromosomal level. DNA and RNA polymerase, SWI/SNF complexes, histone deacetylases, and acetyltransferases are targeted by gene-specific regulators to mediate these structural transitions. The mistargeting of these enzymes contributes to human developmental abnormalities and tumorigenesis. These observations illuminate the roles of chromatin and chromosomal structural biology in human disease.
引用
收藏
页码:102 / 122
页数:21
相关论文
共 193 条
  • [1] A proline-rich TGF-beta-responsive transcriptional activator interacts with histone H3
    Alevizopoulos, A
    Dusserre, Y
    TsaiPflugfelder, M
    vonderWeid, T
    Wahli, W
    Mermod, N
    [J]. GENES & DEVELOPMENT, 1995, 9 (24) : 3051 - 3066
  • [2] Role for N-CoR and histone deacetylase in Sin3-mediated transcriptional repression
    Alland, L
    Muhle, R
    Hou, H
    Potes, J
    Chin, L
    SchreiberAgus, N
    DePinho, RA
    [J]. NATURE, 1997, 387 (6628) : 49 - 55
  • [3] REPLICATION-COUPLED CHROMATIN ASSEMBLY IS REQUIRED FOR THE REPRESSION OF BASAL TRANSCRIPTION IN-VIVO
    ALMOUZNI, G
    WOLFFE, AP
    [J]. GENES & DEVELOPMENT, 1993, 7 (10) : 2033 - 2047
  • [4] Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
    Amir, RE
    Van den Veyver, IB
    Wan, M
    Tran, CQ
    Francke, U
    Zoghbi, HY
    [J]. NATURE GENETICS, 1999, 23 (02) : 185 - 188
  • [5] TREATMENT WITH SODIUM-BUTYRATE INHIBITS THE COMPLETE CONDENSATION OF INTERPHASE CHROMATIN
    ANNUNZIATO, AT
    FRADO, LLY
    SEALE, RL
    WOODCOCK, CLF
    [J]. CHROMOSOMA, 1988, 96 (02) : 132 - 138
  • [6] SPECIFIC PROTECTION OF METHYLATED CPGS IN MAMMALIAN NUCLEI
    ANTEQUERA, F
    MACLEOD, D
    BIRD, AP
    [J]. CELL, 1989, 58 (03) : 509 - 517
  • [7] HIGH-LEVELS OF DENOVO METHYLATION AND ALTERED CHROMATIN STRUCTURE AT CPG ISLANDS IN CELL-LINES
    ANTEQUERA, F
    BOYES, J
    BIRD, A
    [J]. CELL, 1990, 62 (03) : 503 - 514
  • [8] Arenhovel H., 1991, Few-Body Systems Supplementum, P1, DOI 10.1007/978-3-7091-6701-4_1
  • [9] USE OF SELECTIVELY TRYPSINIZED NUCLEOSOME CORE PARTICLES TO ANALYZE THE ROLE OF THE HISTONE TAILS IN THE STABILIZATION OF THE NUCLEOSOME
    AUSIO, J
    DONG, F
    VANHOLDE, KE
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1989, 206 (03) : 451 - 463
  • [10] MAD-MAX TRANSCRIPTIONAL REPRESSION IS MEDIATED BY TERNARY COMPLEX-FORMATION WITH MAMMALIAN HOMOLOGS OF YEAST REPRESSOR SIN3
    AYER, DE
    LAWRENCE, QA
    EISENMAN, RN
    [J]. CELL, 1995, 80 (05) : 767 - 776