Polycomb-like 2 Associates with PRC2 and Regulates Transcriptional Networks during Mouse Embryonic Stem Cell Self-Renewal and Differentiation

被引:151
|
作者
Walker, Emily [1 ]
Chang, Wing Y. [1 ]
Hunkapiller, Julie [4 ]
Cagney, Gerard [5 ,6 ]
Garcha, Kamal [1 ]
Torchia, Joseph [7 ,8 ]
Krogan, Nevan J. [5 ]
Reiter, Jeremy F. [4 ]
Stanford, William L. [1 ,2 ,3 ,9 ]
机构
[1] Univ Toronto, Inst Biomat & Biomed Engn, Toronto, ON M5S 3G9, Canada
[2] Univ Toronto, Inst Med Sci, Toronto, ON M5S 1A8, Canada
[3] Univ Toronto, Dept Chem Engn & Appl Chem, Toronto, ON M5S 3E5, Canada
[4] Univ Calif San Francisco, Cardiovasc Res Inst, Dept Biochem & Biophys, San Francisco, CA 94158 USA
[5] Univ Calif San Francisco, Calif Inst Quantitat Biomed Res, Dept Cellular & Mol Pharmacol, San Francisco, CA 94158 USA
[6] Natl Univ Ireland Univ Coll Dublin, Conway Inst, Dublin 4, Ireland
[7] Lawson Hlth Res Inst, London Reg Canc Program, Dept Oncol & Biochem, London, ON N6A 4L6, Canada
[8] Univ Western Ontario, London, ON N6A 4L6, Canada
[9] Inst Syst Biol, Seattle, WA 98103 USA
关键词
HISTONE METHYLTRANSFERASE ACTIVITY; LEFT-RIGHT ASYMMETRY; ES CELLS; DEVELOPMENTAL REGULATORS; PROTEIN COMPLEXES; RNA INTERFERENCE; ZESTE PROTEIN; PLURIPOTENCY; EXPRESSION; DROSOPHILA;
D O I
10.1016/j.stem.2009.12.014
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Polycomb group (PcG) proteins are conserved epigenetic transcriptional repressors that control numerous developmental gene expression programs and have recently been implicated in modulating embryonic stem cell (ESC) fate. We identified the PcG protein PCL2 (polycomb-like 2) in a genome-wide screen for regulators of self-renewal and pluri-potency and predicted that it would play an important role in mouse ESC-fate determination. Using multiple biochemical strategies, we provide evidence that PCL2 is a Polycomb Repressive Complex 2 (PRC2)-associated protein in mouse ESCs. Knockdown of Pcl2 in ESCs resulted in heightened self-renewal characteristics, defects in differentiation, and altered patterns of histone methylation. Integration of global gene expression and promoter occupancy analyses allowed us to identify PCL2 and PRC2 transcriptional targets and draft regulatory networks. We describe the role of PCL2 in both modulating transcription of ESC self-renewal genes in undifferentiated ESCs as well as developmental regulators during early commitment and differentiation.
引用
收藏
页码:153 / 166
页数:14
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