Co-repressors 2000

被引:168
作者
Burke, LJ [1 ]
Baniahmad, A [1 ]
机构
[1] Univ Giessen, Inst Genet, D-35392 Giessen, Germany
关键词
D O I
10.1096/fj.99-0943rev
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
In the last 5 years, many co-repressors have been identified in eukaryotes that function in a wide range of species, from yeast to Drosophila and humans. Co-repressors are coregulators that are recruited by DNA-bound transcriptional silencers and play essential roles in many pathways including differentiation, proliferation, programmed cell death, and cell cycle. Accordingly, it has been shown that aberrant interactions of co-repressors with transcriptional silencers provide the molecular basis of a variety of human diseases. Co-repressors mediate transcriptional silencing by mechanisms that include direct inhibition of the basal transcription machinery and recruitment of chromatin-modifying enzymes. Chromatin modification includes histone deacetylation, which is thought to lead to a compact chromatin structure to which the accessibility of transcriptional activators is impaired. In a general mechanistic view, the overall picture suggests that transcriptional silencers and co-repressors act in analogy to transcriptional activators and coactivators, but with the opposite effect leading to gene silencing. We provide a comprehensive overview of the currently known higher eukaryotic co-repressors, their mechanism of action, and their involvement in biological and pathophysiological pathways. We also show the different pathways that lead to the regulation of corepressor-silencer complex formation.
引用
收藏
页码:1876 / 1888
页数:13
相关论文
共 164 条
  • [51] Histone deacetylase activity is required for full transcriptional repression by mSin3A
    Hassig, CA
    Fleischer, TC
    Billin, AN
    Schreiber, SL
    Ayer, DE
    [J]. CELL, 1997, 89 (03) : 341 - 347
  • [52] Distinct interactions of PML-RARα and PLZF-RARα with co-repressors determine differential responses to RA in APL
    He, LZ
    Guidez, F
    Tribioli, C
    Peruzzi, D
    Ruthardt, M
    Zelent, A
    Pandolfi, PP
    [J]. NATURE GENETICS, 1998, 18 (02) : 126 - 135
  • [53] A DIRECT LINK BETWEEN CORE HISTONE ACETYLATION AND TRANSCRIPTIONALLY ACTIVE CHROMATIN
    HEBBES, TR
    THORNE, AW
    CRANEROBINSON, C
    [J]. EMBO JOURNAL, 1988, 7 (05) : 1395 - 1402
  • [54] A complex containing N-CoR, mSin3 and histone deacetylase mediates transcriptional repression
    Heinzel, T
    Lavinsky, RM
    Mullen, TM
    Soderstrom, M
    Laherty, CD
    Torchia, J
    Yang, WM
    Brard, G
    Ngo, SD
    Davie, JR
    Seto, E
    Eisenman, RN
    Rose, DW
    Glass, CK
    Rosenfeld, MG
    [J]. NATURE, 1997, 387 (6628) : 43 - 48
  • [55] hFOG-2, a novel zinc finger protein, binds the co-repressor mCtBP2 and modulates GATA-mediated activation
    Holmes, M
    Turner, J
    Fox, A
    Chisholm, O
    Crossley, M
    Chong, B
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (33) : 23491 - 23498
  • [56] Signaling by tyrosine kinases negatively regulates the interaction between transcription factors and SMRT (silencing mediator of retinoic acid and thyroid hormone receptor) corepressor
    Hong, SH
    Wong, CW
    Privalsky, ML
    [J]. MOLECULAR ENDOCRINOLOGY, 1998, 12 (08) : 1161 - 1171
  • [57] SMRT corepressor interacts with PLZF and with the PML-retinoic acid receptor alpha (RAR alpha) and PLZF-RAR alpha oncoproteins associated with acute promyelocytic leukemia
    Hong, SH
    David, G
    Wong, CW
    Dejean, A
    Privalsky, ML
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (17) : 9028 - 9033
  • [58] LIGAND-INDEPENDENT REPRESSION BY THE THYROID-HORMONE RECEPTOR-MEDIATED BY A NUCLEAR RECEPTOR CO-REPRESSOR
    HORLEIN, AJ
    NAAR, AM
    HEINZEL, T
    TORCHIA, J
    GLOSS, B
    KUROKAWA, R
    RYAN, A
    KAMEL, Y
    SODERSTROM, M
    GLASS, CK
    ROSENFELD, MG
    [J]. NATURE, 1995, 377 (6548) : 397 - 404
  • [59] CIR, a corepressor linking the DNA binding factor CBF1 to the histone deacetylase complex
    Hsieh, JJD
    Zhou, SF
    Chen, L
    Young, DB
    Hayward, SD
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (01) : 23 - 28
  • [60] Huang EY, 2000, GENE DEV, V14, P45