The central role of EED in the orchestration of polycomb group complexes

Polycomb repressive complexes 1 and 2 (PRC1 and 2) play a critical role in the epigenetic regulation of transcription during cellular differentiation, stem cell pluripotency and neoplastic progression. Here we show that the polycomb group protein EED, a core component of PRC2, physically interacts w...

Full description

Saved in:
Bibliographic Details
Published in:Nature communications Vol. 5; no. 1; p. 3127
Main Authors: Cao, Qi, Wang, Xiaoju, Zhao, Meng, Yang, Rendong, Malik, Rohit, Qiao, Yuanyuan, Poliakov, Anton, Yocum, Anastasia K., Li, Yong, Chen, Wei, Cao, Xuhong, Jiang, Xia, Dahiya, Arun, Harris, Clair, Feng, Felix Y., Kalantry, Sundeep, Qin, Zhaohui S., Dhanasekaran, Saravana M., Chinnaiyan, Arul M.
Format: Journal Article
Language:English
Published: London Nature Publishing Group UK 01-01-2014
Nature Publishing Group
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Polycomb repressive complexes 1 and 2 (PRC1 and 2) play a critical role in the epigenetic regulation of transcription during cellular differentiation, stem cell pluripotency and neoplastic progression. Here we show that the polycomb group protein EED, a core component of PRC2, physically interacts with and functions as part of PRC1. Components of PRC1 and PRC2 compete for EED binding. EED functions to recruit PRC1 to H3K27me3 loci and enhances PRC1-mediated H2A ubiquitin E3 ligase activity. Taken together, we suggest an integral role for EED as an epigenetic exchange factor coordinating the activities of PRC1 and 2. Polycomb group proteins are epigenetic gene silencers that are thought to exist in two biochemically distinct multiprotein complexes, termed PRC-1 and -2. Here, Cao et al. show that EED, a core component of PRC2, interacts with and functions as part of PRC1, thus coordinating the activities of both complexes.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms4127