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

Qi Cao; Xiaoju Wang; Meng Zhao; Rendong Yang; Rohit Malik; Yuanyuan Qiao; Anton Poliakov; Anastasia K. Yocum; Yong Li; Wei Chen; Xuhong Cao; Xia Jiang; Arun Dahiya; Clair Harris; Felix Y. Feng; Sundeep Kalantry; Zhaohui S. Qin; Saravana M. Dhanasekaran; Arul M. Chinnaiyan

doi:10.1038/ncomms4127

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

Qi Cao, Xiaoju Wang, Meng Zhao, Rendong Yang, Rohit Malik, Yuanyuan Qiao, Anton Poliakov, Anastasia K. Yocum, Yong Li, Wei Chen, Xuhong Cao, Xia Jiang, Arun Dahiya, Clair Harris, Felix Y. Feng, Sundeep Kalantry, Zhaohui S. Qin, Saravana M. Dhanasekaran, Arul M. Chinnaiyan^*

^*Corresponding author for this work

Urology

Research output: Contribution to journal › Article › peer-review

114 Scopus citations

Abstract

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.

Original language	English (US)
Article number	3127
Journal	Nature communications
Volume	5
DOIs	https://doi.org/10.1038/ncomms4127
State	Published - Jan 24 2014

ASJC Scopus subject areas

Physics and Astronomy(all)
Chemistry(all)
Biochemistry, Genetics and Molecular Biology(all)

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10.1038/ncomms4127

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Cao, Q., Wang, X., Zhao, M., Yang, R., Malik, R., Qiao, Y., Poliakov, A., Yocum, A. K., Li, Y., Chen, W., Cao, X., Jiang, X., Dahiya, A., Harris, C., Feng, F. Y., Kalantry, S., Qin, Z. S., Dhanasekaran, S. M., & Chinnaiyan, A. M. (2014). The central role of EED in the orchestration of polycomb group complexes. Nature communications, 5, Article 3127. https://doi.org/10.1038/ncomms4127

@article{66178c81f22d418d8b70571f9bd98099,

title = "The central role of EED in the orchestration of polycomb group complexes",

abstract = "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.",

author = "Qi Cao and Xiaoju Wang and Meng Zhao and Rendong Yang and Rohit Malik and Yuanyuan Qiao and Anton Poliakov and Yocum, {Anastasia K.} and Yong Li and Wei Chen and Xuhong Cao and Xia Jiang and Arun Dahiya and Clair Harris and Feng, {Felix Y.} and Sundeep Kalantry and Qin, {Zhaohui S.} and Dhanasekaran, {Saravana M.} and Chinnaiyan, {Arul M.}",

note = "Funding Information: We thank Dr Terry Magnuson for the Eed−/− mESCs cells, Cynthia Wang for protein purification, Ingrid J. Apel for AlphaScreen assays, Javed Siddiqui, Rui Wang, Wei Yan, Yaqing Zhang, Rong Zhao, Maria Chen, Kari Wilder-Romans for technical assistance, Terry Barrette for database management, the University of Michigan Vector Core for generating adenovirus and lentivirus, Ram Mani, J. Chad Brenner, Irfan A. Asangani for discussions, and Jyoti Athanikar and Karen Giles for critically reading the manuscript and submitting documents. The confocal immunofluorescence colocalization analysis was performed in the Microscopy and Image-analysis Laboratory (MIL) at the University of Michigan, Department of Cell & Developmental Biology. This work is supported in part by the Prostate SPORE P50CA69568 and National Institutes of Health (R01CA132874). A.M.C. is supported by the Prostate Cancer Foundation (PCF), the Doris Duke Charitable Foundation, and the Howard Hughes Medical Institute. A.M.C. is an American Cancer Society Research Professor and A. Alfred Taubman Scholar. Q.C. is supported by the US Department of Defense (PC094725) and a Young Investigator Award from the PCF; F.Y.F. is supported by a Young Investigator Award from the PCF; S.K. is supported by an NIH Director{\textquoteright}s New Innovator Award (DP2-OD-008646-01) and a March of Dimes Basil O{\textquoteright}Connor Starter Scholar Research Award; M.Z. and Z.S.Q. are supported by National Institutes of Health (7R01HG005119-02).",

year = "2014",

month = jan,

day = "24",

doi = "10.1038/ncomms4127",

language = "English (US)",

volume = "5",

journal = "Nature communications",

issn = "2041-1723",

publisher = "Nature Publishing Group",

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TY - JOUR

T1 - The central role of EED in the orchestration of polycomb group complexes

AU - Cao, Qi

AU - Wang, Xiaoju

AU - Zhao, Meng

AU - Yang, Rendong

AU - Malik, Rohit

AU - Qiao, Yuanyuan

AU - Poliakov, Anton

AU - Yocum, Anastasia K.

AU - Li, Yong

AU - Chen, Wei

AU - Cao, Xuhong

AU - Jiang, Xia

AU - Dahiya, Arun

AU - Harris, Clair

AU - Feng, Felix Y.

AU - Kalantry, Sundeep

AU - Qin, Zhaohui S.

AU - Dhanasekaran, Saravana M.

AU - Chinnaiyan, Arul M.

N1 - Funding Information: We thank Dr Terry Magnuson for the Eed−/− mESCs cells, Cynthia Wang for protein purification, Ingrid J. Apel for AlphaScreen assays, Javed Siddiqui, Rui Wang, Wei Yan, Yaqing Zhang, Rong Zhao, Maria Chen, Kari Wilder-Romans for technical assistance, Terry Barrette for database management, the University of Michigan Vector Core for generating adenovirus and lentivirus, Ram Mani, J. Chad Brenner, Irfan A. Asangani for discussions, and Jyoti Athanikar and Karen Giles for critically reading the manuscript and submitting documents. The confocal immunofluorescence colocalization analysis was performed in the Microscopy and Image-analysis Laboratory (MIL) at the University of Michigan, Department of Cell & Developmental Biology. This work is supported in part by the Prostate SPORE P50CA69568 and National Institutes of Health (R01CA132874). A.M.C. is supported by the Prostate Cancer Foundation (PCF), the Doris Duke Charitable Foundation, and the Howard Hughes Medical Institute. A.M.C. is an American Cancer Society Research Professor and A. Alfred Taubman Scholar. Q.C. is supported by the US Department of Defense (PC094725) and a Young Investigator Award from the PCF; F.Y.F. is supported by a Young Investigator Award from the PCF; S.K. is supported by an NIH Director’s New Innovator Award (DP2-OD-008646-01) and a March of Dimes Basil O’Connor Starter Scholar Research Award; M.Z. and Z.S.Q. are supported by National Institutes of Health (7R01HG005119-02).

PY - 2014/1/24

Y1 - 2014/1/24

N2 - 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.

AB - 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.

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DO - 10.1038/ncomms4127

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SN - 2041-1723

VL - 5

JO - Nature communications

JF - Nature communications

M1 - 3127

ER -

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

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