Molecular biology of the Ets family of transcription factors

被引:550
作者
Oikawa, T [1 ]
Yamada, T [1 ]
机构
[1] Sasaki Inst, Dept Cell Genet, Chiyoda Ku, Tokyo 1010062, Japan
关键词
Ets transcription factor; growth; differentiation; apoptosis; leukemia; tumor cell; malignancy;
D O I
10.1016/S0378-1119(02)01156-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The Ets family of transcription factors characterized by an evolutionarily-conserved DNA-binding domain regulates expression of a variety of viral and cellular genes by binding to a purine-rich GGAA/T core sequence in cooperation with other transcriptional factors and co-factors. Most Ets family proteins are nuclear targets for activation of Ras-MAP kinase signaling pathway and some of them affect proliferation of cells by regulating the immediate early response genes and other growth-related genes. Some of them also regulate apoptosis-related genes. Several Ets family proteins are preferentially expressed in specific cell lineages and are involved in their development and differentiation by increasing the enhancer or promoter activities of the genes encoding growth factor receptors and integrin families specific for the cell lineages. Many Ets family proteins also modulate gene expression through protein-protein interactions with other cellular partners. Deregulated expression or formation of chimeric fusion proteins of Ets family due to proviral insertion or chromosome translocation is associated with leukemias and specific types of solid tumors. Several Ets family proteins also participate in malignancy of tumor cells including invasion and metastasis by activating the transcription of several protease genes and angiogenesis-related genes. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:11 / 34
页数:24
相关论文
共 286 条
  • [31] Carron C, 2000, BLOOD, V95, P3891
  • [32] c-Fos oncogene regulator Elk-1 interacts with BRCA1 splice variants BRCA1a/1b and enhances BRCA1a/1b-mediated growth suppression in breast cancer cells
    Chai, YL
    Chipitsyna, G
    Cui, JQ
    Liao, BS
    Liu, S
    Aysola, K
    Yezdani, M
    Reddy, ESP
    Rao, VN
    [J]. ONCOGENE, 2001, 20 (11) : 1357 - 1367
  • [33] Posttranslational modification of TEL and TEL/AML1 by SUMO-1 and cell-cycle-dependent assembly into nuclear bodies
    Chakrabarti, SR
    Sood, R
    Nandi, S
    Nucifora, G
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (24) : 13281 - 13285
  • [34] 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
  • [35] Modulation of TEL transcription activity by interaction with the ubiquitin-conjugating enzyme UBC9
    Chakrabarti, SR
    Sood, R
    Ganguly, S
    Bohlander, S
    Shen, ZY
    Nucifora, G
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (13) : 7467 - 7472
  • [36] Over-expression of ERT(ESX/ESE-1/ELF3), an ets-related transcription factor, induces endogenous TGF-β type II receptor expression and restores the TGF-β signaling pathway in Hs578t human breast cancer cells
    Chang, J
    Lee, C
    Hahm, KB
    Yi, Y
    Choi, SG
    Kim, SJ
    [J]. ONCOGENE, 2000, 19 (01) : 151 - 154
  • [37] Activity of the distal positive element of the peripherin gene is dependent on proteins binding to an Ets-like recognition site and a novel inverted repeat site
    Chang, LF
    Thompson, MA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (11) : 6467 - 6475
  • [38] The Rel/NF-κB family directly activates expression of the apoptosis inhibitor Bcl-xL
    Chen, CL
    Edelstein, LC
    Gélinas, C
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (08) : 2687 - 2695
  • [39] CHEN MH, 1996, HELICOBACTER, V1, P271
  • [40] Chen ZQ, 1997, CANCER RES, V57, P2013