Negative regulation of transcription coactivator p300 by orphan receptor TR3

被引:17
作者
Li, Gui-Deng [1 ]
Fang, Jin-Xu [1 ]
Chen, Hang-Zi [1 ]
Luo, Jie [1 ]
Zheng, Zhong-Hui [1 ]
Shen, Yue-Mao [1 ]
Wu, Qiao [1 ]
机构
[1] Xiamen Univ, Sch Life Sci, Key Lab Minist Educ Cell Biol & Tumor Cell Engn, Xiamen 361005, Peoples R China
基金
中国国家自然科学基金;
关键词
D O I
10.1093/nar/gkm870
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
p300 regulates the transcriptional activity of a variety of transcription factors by forming an activation complex and/or promoting histone acetylation. Here, we show a unique characteristic of orphan receptor TR3 in negatively regulating the function of p300. TR3 was found to interact with p300 and inhibited the acetylation of transcription factors induced by p300, resulting in the repression of their transcriptional activity. Further analysis revealed that both a conserved transcriptional adapter motif (TRAM) in p300 and a specific sequence FLELFIL in TR3 were critical for their interaction. TR3 binding completely covered the histone acetyltransferase (HAT) domain of p300 and resulted in suppression of the HAT activity, as the p300-induced histone H3 acetylation and transcription were inhibited with the presence TR3. Furthermore, an agonist of TR3, a natural octaketide isolated from Dothiorella sp. HTF3 of an endophytical fungus, was shown to be a potent compound for inhibiting p300 HAT activity (IC50=1.5 mu g/ml) in vivo. More importantly, this agonist could repress the transcriptional activity of transcription factors, and proliferation of cancer cells. Taken together, our results not only delineate a novel transcriptional repressor function for TR3, but also reveal its modulation on p300 HAT activity as the underlying mechanism.
引用
收藏
页码:7348 / 7359
页数:12
相关论文
共 48 条
  • [1] Curcumin, a novel p300/CREB-binding protein-specific inhibitor of acetyltransferase, represses the acetylation of histone/nonhistone proteins and histone acetyltransferase-dependent chromatin transcription
    Balasubramanyam, K
    Varier, RA
    Altaf, M
    Swaminathan, V
    Siddappa, NB
    Ranga, U
    Kundu, TK
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (49) : 51163 - 51171
  • [2] Polyisoprenylated benzophenone, garcinol, a natural histone acetyltransferase inhibitor, represses chromatin transcription and alters global gene expression
    Balasubramanyam, K
    Altaf, M
    Varier, RA
    Swaminathan, V
    Ravindran, A
    Sadhale, PP
    Kundu, TK
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (32) : 33716 - 33726
  • [3] The CBP co-activator is a histone acetyltransferase
    Bannister, AJ
    Kouzarides, T
    [J]. NATURE, 1996, 384 (6610) : 641 - 643
  • [4] Burysek L, 1999, J VIROL, V73, P7334
  • [5] A viral mechanism for inhibition of p300 and PCAF acetyltransferase activity
    Chakravarti, D
    Ogryzko, V
    Kao, HY
    Nash, A
    Chen, HW
    Nakatani, Y
    Evans, RM
    [J]. CELL, 1999, 96 (03) : 393 - 403
  • [6] Duration of nuclear NF-κB action regulated by reversible acetylation
    Chen, LF
    Fischle, W
    Verdin, E
    Greene, WC
    [J]. SCIENCE, 2001, 293 (5535) : 1653 - 1657
  • [7] Activation of Nur77 by selected 1,1-bis(3'-indolyl)-1-(p-substituted phenyl) methanes induces apoptosis through nuclear pathways
    Chintharlapalli, S
    Burghardt, R
    Papineni, S
    Ramaiah, S
    Yoon, K
    Safe, S
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (26) : 24903 - 24914
  • [8] HDAC7, a thymus-specific class II histone deacetylase, regulates Nur77 transcription and TCR-mediated apoptosis
    Dequiedt, F
    Kasler, H
    Fischle, W
    Kiermer, V
    Weinstein, M
    Herndier, BG
    Verdin, E
    [J]. IMMUNITY, 2003, 18 (05) : 687 - 698
  • [9] MOLECULAR-CLONING AND FUNCTIONAL ANAL OF THE ADENOVIRUS E1A-ASSOCIATED 300-KD PROTEIN (P300) REVEALS A PROTEIN WITH PROPERTIES OF A TRANSCRIPTIONAL ADAPTER
    ECKNER, R
    EWEN, ME
    NEWSOME, D
    GERDES, M
    DECAPRIO, JA
    LAWRENCE, JB
    LIVINGSTON, DM
    [J]. GENES & DEVELOPMENT, 1994, 8 (08) : 869 - 884
  • [10] UNIQUE RESPONSE PATHWAYS ARE ESTABLISHED BY ALLOSTERIC INTERACTIONS AMONG NUCLEAR HORMONE RECEPTORS
    FORMAN, BM
    UMESONO, K
    CHEN, J
    EVANS, RM
    [J]. CELL, 1995, 81 (04) : 541 - 550