Breast cancer associated transcriptional repressor PLU-1/JARID1B interacts directly with histone deacetylases

被引:78
作者
Barrett, Angela
Santangelo, Samantha
Tan, Keith
Catchpole, Steve
Roberts, Kevin
Spencer-Dene, Bradley
Hall, Debbie
Scibetta, Angelo
Burchell, Joy
Verdin, Eric
Freemont, Paul
Taylor-Papadimitriou, Joyce
机构
[1] Kings Coll London, Canc Res UK, Breast Canc Biol Grp, Guys Hosp, London SE1 9RT, England
[2] Imperial Coll London, Div Mol Biosci, London, England
[3] UCL, Canc Res Technol Ltd, Wolfson Inst Biomed Res, London, England
[4] Imperial Coll London, Dept Histopathol, London, England
[5] Canc Res UK, London Res Inst, Expt Pathol Lab, London, England
[6] Univ Calif San Francisco, Gladstone Inst Virol & Immunol, San Francisco, CA 94143 USA
关键词
PLU-1/JARID1B; breast cancer; transcriptional repression; histone deacetylases;
D O I
10.1002/ijc.22673
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The PLU-1/JARID1B nuclear protein, which is expressed in a high proportion of breast cancers, but shows restricted expression elsewhere, belongs to the ARID family of proteins, known to play important roles in development, differentiation, transcriptional regulation and chromatin remodeling. PLU-1/JARID1B is a strong transcriptional repressor, and here we show that the protein localizes in MAD bodies when cotransfected with class IIa histone deacetylases (HDACs) or N-CoR. Direct binding to class I and class IIa HDACs is demonstrated, while the interaction with N-CoR appears to be indirect. The domains involved in the HDAC4-PLU-1/JARID1B interaction were investigated in detail, and the data show that 2 PHD domains in PLU-1/JARID1B, which are involved in transcriptional repression, are also crucial for binding to a domain in the 5' region of HDAC4, overlapping the MEF-2 binding region. Physiological relevance of this interaction in the mammary gland is suggested from the observation that HDAC4 and PLU-1/JARID1B are coexpressed in the pregnant and involuting mouse mammary gland and are both silenced at lactation. Significantly, the expression of both proteins is seen in breast cancers. (c) 2007 Wiley-Liss, lnc.
引用
收藏
页码:265 / 275
页数:11
相关论文
共 41 条
[31]  
TAN K, 2003, J BIOL CHEM, V25, P25
[32]   Chromatin deacetylation by an ATP-dependent nucleosome remodelling complex [J].
Tong, JK ;
Hassig, CA ;
Schnitzler, GR ;
Kingston, RE ;
Schreiber, SL .
NATURE, 1998, 395 (6705) :917-921
[33]   Histone demethylation by a family of JmjC domain-containing proteins [J].
Tsukada, Y ;
Fang, J ;
Erdjument-Bromage, H ;
Warren, ME ;
Borchers, CH ;
Tempst, P ;
Zhang, Y .
NATURE, 2006, 439 (7078) :811-816
[34]   A novel nuclear receptor corepressor complex, N-CoR, contains components of the mammalian SWI/SNF complex and the corepressor KAP-1 [J].
Underhill, C ;
Qutob, MS ;
Yee, SP ;
Torchia, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (51) :40463-40470
[35]   Class II histone deacetylases: versatile regulators [J].
Verdin, E ;
Dequiedt, F ;
Kasler, HG .
TRENDS IN GENETICS, 2003, 19 (05) :286-293
[36]   Nomenclature of the ARID family of DNA-binding proteins [J].
Wilsker, D ;
Probst, L ;
Wain, HM ;
Maltais, L ;
Tueker, PW ;
Moran, E .
GENOMICS, 2005, 86 (02) :242-251
[37]   JHDM2A, a JmjC-containing H3K9 dernethylase, facilitates transcription activation by androgen receptor [J].
Yamane, Kenichi ;
Toumazou, Charalambos ;
Tsukada, Yu-ichi ;
Erdjument-Bromage, Hediye ;
Tempst, Paul ;
Wong, Jiemin ;
Zhang, Yi .
CELL, 2006, 125 (03) :483-495
[38]   Isolation and characterization of cDNAs corresponding to an additional member of the human histone deacetylase gene family [J].
Yang, WM ;
Yao, YL ;
Sun, JM ;
Davie, JR ;
Seto, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (44) :28001-28007
[39]   Class II histone deacetylases:: from sequence to function, regulation, and clinical implication [J].
Yang, XJ ;
Grégoire, S .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (08) :2873-2884
[40]   The dermatomyositis-specific autoantigen Mi2 is a component of a complex containing histone deacetylase and nucleosome remodeling activities [J].
Zhang, Y ;
LeRoy, G ;
Seelig, HP ;
Lane, WS ;
Reinberg, D .
CELL, 1998, 95 (02) :279-289