Role of the polycomb protein EED in the propagation of repressive histone marks

被引:878
作者
Margueron, Raphael [2 ,3 ]
Justin, Neil [4 ]
Ohno, Katsuhito [1 ]
Sharpe, Miriam L. [4 ]
Son, Jinsook [2 ,3 ]
Drury, William J., III [2 ,3 ]
Voigt, Philipp [2 ,3 ]
Martin, Stephen R. [4 ]
Taylor, William R. [4 ]
De Marco, Valeria [4 ]
Pirrotta, Vincenzo [1 ]
Reinberg, Danny [2 ,3 ]
Gamblin, Steven J. [4 ]
机构
[1] Rutgers State Univ, Dept Mol Biol & Biochem, Nelson Labs, Piscataway, NJ 08854 USA
[2] NYU, Sch Med, Howard Hughes Med Inst, New York, NY 10016 USA
[3] NYU, Sch Med, Dept Biochem, New York, NY 10016 USA
[4] MRC Natl Inst Med Res, London NW7 1AA, England
关键词
METHYLTRANSFERASE ACTIVITY; STRUCTURAL BASIS; DROSOPHILA; RECOGNITION; H3; TRIMETHYLATION; ESC; METHYLATION; COMPLEXES; CHROMATIN;
D O I
10.1038/nature08398
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Polycomb group proteins have an essential role in the epigenetic maintenance of repressive chromatin states. The gene-silencing activity of the Polycomb repressive complex 2 (PRC2) depends on its ability to trimethylate lysine 27 of histone H3 (H3K27) by the catalytic SET domain of the EZH2 subunit, and at least two other subunits of the complex: SUZ12 and EED. Here we show that the carboxy-terminal domain of EED specifically binds to histone tails carrying trimethyl-lysine residues associated with repressive chromatin marks, and that this leads to the allosteric activation of the methyltransferase activity of PRC2. Mutations in EED that prevent it from recognizing repressive trimethyl-lysine marks abolish the activation of PRC2 in vitro and, in Drosophila, reduce global methylation and disrupt development. These findings suggest a model for the propagation of the H3K27me3 mark that accounts for the maintenance of repressive chromatin domains and for the transmission of a histone modification from mother to daughter cells.
引用
收藏
页码:762 / U11
页数:8
相关论文
共 40 条
[1]   THE CCP4 SUITE - PROGRAMS FOR PROTEIN CRYSTALLOGRAPHY [J].
BAILEY, S .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1994, 50 :760-763
[2]   Site-specific transformation of Drosophila via φC31 integrase-mediated cassette exchange [J].
Bateman, Jack R. ;
Lee, Anne M. ;
Wu, C. -ting .
GENETICS, 2006, 173 (02) :769-777
[3]   An optimized transgenesis system for Drosophila using germ-line-specific φC31 integrases [J].
Bischof, Johannes ;
Maeda, Robert K. ;
Hediger, Monika ;
Karch, Francois ;
Basler, Konrad .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (09) :3312-3317
[4]   Crystallography & NMR system:: A new software suite for macromolecular structure determination [J].
Brunger, AT ;
Adams, PD ;
Clore, GM ;
DeLano, WL ;
Gros, P ;
Grosse-Kunstleve, RW ;
Jiang, JS ;
Kuszewski, J ;
Nilges, M ;
Pannu, NS ;
Read, RJ ;
Rice, LM ;
Simonson, T ;
Warren, GL .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1998, 54 :905-921
[5]   Role of histone H3 lysine 27 methylation in polycomb-group silencing [J].
Cao, R ;
Wang, LJ ;
Wang, HB ;
Xia, L ;
Erdjument-Bromage, H ;
Tempst, P ;
Jones, RS ;
Zhang, Y .
SCIENCE, 2002, 298 (5595) :1039-1043
[6]   Drosophila enhancer of Zeste/ESC complexes have a histone H3 methyltransferase activity that marks chromosomal polycomb sites [J].
Czermin, B ;
Melfi, R ;
McCabe, D ;
Seitz, V ;
Imhof, A ;
Pirrotta, V .
CELL, 2002, 111 (02) :185-196
[7]   Coot:: model-building tools for molecular graphics [J].
Emsley, P ;
Cowtan, K .
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY, 2004, 60 :2126-2132
[8]   Structural basis of EZH2 recognition by EED [J].
Han, Zhifu ;
Xing, Xinmiao ;
Hu, Min ;
Zhang, Yin ;
Liu, Peiyuan ;
Chai, Jijie .
STRUCTURE, 2007, 15 (10) :1306-1315
[9]   A model for transmission of the H3K27me3 epigenetic mark [J].
Hansen, Klaus H. ;
Bracken, Adrian P. ;
Pasini, Diego ;
Dietrich, Nikolaj ;
Gehani, Simmi S. ;
Monrad, Astrid ;
Rappsilber, Juri ;
Lerdrup, Mads ;
Helin, Kristian .
NATURE CELL BIOLOGY, 2008, 10 (11) :1291-U89
[10]   Recognition of histone H3 lysine-4 methylation by the double tudor domain of JMJD2A [J].
Huang, Y ;
Fang, J ;
Bedford, MT ;
Zhang, Y ;
Xu, RM .
SCIENCE, 2006, 312 (5774) :748-751