Role of Histone H3 Lysine 27 Methylation in Polycomb-Group Silencing

Author:

Cao Ru12,Wang Liangjun3,Wang Hengbin1,Xia Li1,Erdjument-Bromage Hediye4,Tempst Paul4,Jones Richard S.3,Zhang Yi12

Affiliation:

1. Department of Biochemistry and Biophysics, Lineberger Comprehensive Cancer Center,

2. Curriculum in Genetics and Molecular Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599–7295, USA.

3. Department of Biological Sciences, Southern Methodist University, Dallas, TX 75275, USA.

4. Molecular Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10021, USA.

Abstract

Polycomb group (PcG) proteins play important roles in maintaining the silent state of HOX genes. Recent studies have implicated histone methylation in long-term gene silencing. However, a connection between PcG-mediated gene silencing and histone methylation has not been established. Here we report the purification and characterization of an EED-EZH2 complex, the human counterpart of the Drosophila ESC-E(Z) complex. We demonstrate that the complex specifically methylates nucleosomal histone H3 at lysine 27 (H3-K27). Using chromatin immunoprecipitation assays, we show that H3-K27 methylation colocalizes with, and is dependent on, E(Z) binding at an Ultrabithorax ( Ubx ) Polycomb response element (PRE), and that this methylation correlates with Ubx repression. Methylation on H3-K27 facilitates binding of Polycomb (PC), a component of the PRC1 complex, to histone H3 amino-terminal tail. Thus, these studies establish a link between histone methylation and PcG-mediated gene silencing.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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