Tip60 is a co-repressor for STAT3

被引:97
作者
Xiao, H
Chung, J
Kao, HY
Yang, YC
机构
[1] Case Western Reserve Univ, Sch Med, Dept Pharmacol, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Sch Med, Ctr Canc, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Sch Med, Dept Biochem, Cleveland, OH 44106 USA
关键词
D O I
10.1074/jbc.M210816200
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
Tip60 (Tat-interactive protein, 60 kDa), a cellular protein with intrinsic histone acetyltransferase activity, is involved in DNA damage repair and apoptosis. Recent studies have suggested that Tip60 acts either as a coactivator or a co-repressor to modulate transcription. In this study, we demonstrate that Tip60 represses reporter gene expression when it is fused to the Ga14 DNA binding domain. We also show that Tip60 associates with histone deacetylase 7 (HDAC7) through its N-terminal zinc finger-containing region and that HDAC7 activity is required for the repressive effect of Tip60. Because endogenous Tip60 interacts with STAT3, we hypothesized that Tip60 might complex with STAT3 and HDAC7 and modulate STAT3-mediated trans-activation. Consistent with this hypothesis, the overexpression of Tip60 represses STAT3-driven reporter gene expression, which can be further potentiated by the co-transfection of HDAC7. Furthermore, interleukin-9-induced c-myc expression, which depends on STAT3 activity, is abrogated by exogenous expression of Tip60. This is the first demonstration of which Tip60 represses STAT3 activity in part through the recruitment of HDAC7.
引用
收藏
页码:11197 / 11204
页数:8
相关论文
共 60 条
[31]   Interleukin 9 induces expression of three cytokine signal inhibitors: cytokine-inducible SH2-containing protein, suppressor of cytokine signalling (SOCS)-2 and SOCS-3, but only SOCS-3 overexpression suppresses interleukin 9 signalling [J].
Lejeune, D ;
Demoulin, JB ;
Renauld, JC .
BIOCHEMICAL JOURNAL, 2001, 353 :109-116
[32]   Class II histone deacetylases are directly recruited by BCL6 transcriptional repressor [J].
Lemercier, C ;
Brocard, MP ;
Puvion-Dutilleul, F ;
Kao, HY ;
Albagli, O ;
Khochbin, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (24) :22045-22052
[33]   Both corepressor proteins SMRT and N-CoR exist in large protein complexes containing HDAC3 [J].
Li, JW ;
Wang, J ;
Wang, JX ;
Nawaz, Z ;
Liu, JM ;
Qin, J ;
Wong, JM .
EMBO JOURNAL, 2000, 19 (16) :4342-4350
[34]   Role of the histone deacetylase complex in acute promyelocytic leukaemia [J].
Lin, RJ ;
Nagy, L ;
Inoue, S ;
Shao, WL ;
Miller, WH ;
Evans, RM .
NATURE, 1998, 391 (6669) :811-814
[35]   Transient expression of TIP60 protein during early chick heart development [J].
Lough, JW .
DEVELOPMENTAL DYNAMICS, 2002, 223 (03) :419-425
[36]   Characterization and expression of the mouse tat interactive protein 60 kD (TIP60) gene [J].
McAllister, D ;
Merlo, X ;
Lough, J .
GENE, 2002, 289 (1-2) :169-176
[37]   HDAC4 deacetylase associates with and represses the MEF2 transcription factor [J].
Miska, EA ;
Karlsson, C ;
Langley, E ;
Nielsen, SJ ;
Pines, J ;
Kouzarides, T .
EMBO JOURNAL, 1999, 18 (18) :5099-5107
[38]   Synergistic signaling in fetal brain by STAT3-Smad1 complex bridged by p300 [J].
Nakashima, K ;
Yanagisawa, M ;
Arakawa, H ;
Kimura, N ;
Hisatsune, T ;
Kawabata, M ;
Miyazono, K ;
Taga, T .
SCIENCE, 1999, 284 (5413) :479-482
[39]   The yeast SAS (something about silencing) protein complex contains a MYST-type putative acetyltransferase and functions with chromatin assembly factor ASF1 [J].
Osada, S ;
Sutton, A ;
Muster, N ;
Brown, CE ;
Yates, JR ;
Sternglanz, R ;
Workman, JL .
GENES & DEVELOPMENT, 2001, 15 (23) :3155-3168
[40]  
RAN Q, 2002, GENE, V258, P169