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

Ru Cao(University of North Carolina at Chapel Hill), Liangjun Wang(Southern Methodist University), Hengbin Wang(Segeberger Kliniken), Li Xia(Segeberger Kliniken), Hediye Erdjument‐Bromage(Memorial Sloan Kettering Cancer Center), Paul Tempst(Memorial Sloan Kettering Cancer Center), Richard S. Jones(Southern Methodist University), Yi Zhang(University of North Carolina at Chapel Hill)
Science
October 31, 2002
Cited by 3,773

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.


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