Proteins of the ETS family with transcriptional repressor activity

被引:112
作者
Mavrothalassitis, G [1 ]
Ghysdael, J
机构
[1] Univ Crete, Sch Med, Heraklion 71409, Crete, Greece
[2] FORTH, IMBB, Heraklion 71409, Crete, Greece
[3] Ctr Univ Orsay, Inst Curie, CNRS, UMR 146, F-91405 Orsay, France
关键词
ets; repression; transcription; proliferation;
D O I
10.1038/sj.onc.1204045
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
ETS proteins form one of the largest families of signal-dependent transcriptional regulators, mediating cellular proliferation, differentiation and tumorigenesis, Most of the known ETS proteins have been shown to activate transcription. However, four ETS proteins (YAN, ERF, NET and TEL) can act as transcriptional repressors. In three cases (ERF, NET and TEL) distinct repression domains have been identified and there are indications that NET and TEL may mediate transcription via Histone Deacetylase recruitment. All four proteins appear to be regulated by MAPKs, though for YAN and ERF this regulation seems to be restricted to ERKs, YAN, ERF and TEL have been implicated in cellular proliferation although there are indications suggesting a possible involvement of YAN and TEL in differentiation as well. Other ETS-domain proteins have been shown to repress transcription in a context specific manner, and there are suggestions that the ETS DNA-binding domain may act as a transcriptional repressor. Transcriptional repression by ETS domain proteins adds an other level in the orchestrated regulation by this diverse family of transcription factors that often recognize similar if not identical binding sites on DNA and are believed to regulate critical genes in a variety of biological processes. Definitive assessment of the importance of this novel regulatory level will require the identification of ETS proteins target genes and the further analysis of transcriptional control and biological function of these proteins in defined pathways.
引用
收藏
页码:6524 / 6532
页数:9
相关论文
共 110 条
  • [1] Suppression of the Ewing's sarcoma phenotype by FLI1/ERF repressor hybrids
    Athanasiou, M
    LeGallic, L
    Watson, DK
    Blair, DG
    Mavrothalassitis, G
    [J]. CANCER GENE THERAPY, 2000, 7 (08) : 1188 - 1195
  • [2] Genomic organization of TEL: The human ETS-variant gene 6
    Baens, M
    Peeters, P
    Guo, CY
    Aerssens, J
    Marynen, P
    [J]. GENOME RESEARCH, 1996, 6 (05): : 404 - 413
  • [3] Methylation-induced repression - Belts, braces, and chromatin
    Bird, AP
    Wolffe, AP
    [J]. CELL, 1999, 99 (05) : 451 - 454
  • [4] REPRESSION OF I-A-BETA GENE-EXPRESSION BY THE TRANSCRIPTION FACTOR PU.1
    BORRAS, FE
    LLOBERAS, J
    MAKI, RA
    CELADA, A
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (41) : 24385 - 24391
  • [5] RAPID AND TRANSIENT EXPRESSION OF ETS2 IN MATURE MACROPHAGES FOLLOWING STIMULATION WITH CMGF, LPS, AND PKC ACTIVATORS
    BOULUKOS, KE
    POGNONEC, P
    SARIBAN, E
    BAILLY, M
    LAGROU, C
    GHYSDAEL, J
    [J]. GENES & DEVELOPMENT, 1990, 4 (03) : 401 - 409
  • [6] Lineage commitment in lymphopoiesis
    Busslinger, M
    Nutt, SL
    Rolink, AG
    [J]. CURRENT OPINION IN IMMUNOLOGY, 2000, 12 (02) : 151 - 158
  • [7] The TEL platelet-derived growth factor beta receptor (PDGF beta R) fusion in chronic myelomonocytic leukemia is a transforming protein that self-associates and activates PDGF beta R kinase-dependent signaling pathways
    Carroll, M
    Tomasson, MH
    Barker, GF
    Golub, TR
    Gilliland, DG
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) : 14845 - 14850
  • [8] Carron C, 2000, BLOOD, V95, P3891
  • [9] The leukemia-associated gene TEL encodes a transcription repressor which associates with SMRT and mSin3A
    Chakrabarti, SR
    Nucifora, G
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 264 (03) : 871 - 877
  • [10] Cowley DO, 2000, GENE DEV, V14, P366