The transcriptional repressor NIPP1 is an essential player in EZH2-mediated gene silencing

被引:66
|
作者
Nuytten, M. [1 ]
Beke, L. [1 ]
Van Eynde, A. [1 ]
Ceulemans, H. [1 ]
Beullens, M. [1 ]
Van Hummelen, P. [2 ]
Fuks, F. [3 ]
Bollen, M. [1 ]
机构
[1] Katholieke Univ Leuven, Fac Med, Dept Mol Cell Biol, Lab Biosignaling & Therapeut, B-3000 Louvain, Belgium
[2] VIB, Microarray Facil, Louvain, Belgium
[3] Free Univ Brussels, Fac Med, Lab Canc Epigenet, Louvain, Belgium
关键词
EZH2; gene silencing; NIPP1; polycomb group proteins; PRC2; transcriptional repression;
D O I
10.1038/sj.onc.1210774
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
EZH2 is a Polycomb group (PcG) protein that promotes the late-stage development of cancer by silencing a specific set of genes, at least in part through trimethylation of associated histone H3 on Lys 27 (H3K27). Nuclear inhibitor of protein phosphatase-1 (NIPP1) is a ubiquitously expressed transcriptional repressor that has binding sites for the EZH2 interactor EED. Here, we examine the contribution of NIPP1 to EZH2-mediated gene silencing. Studies on NIPP1-deficient cells disclose a widespread and essential role of NIPP1 in the trimethylation of H3K27 by EZH2, not only in the onset of this trimethylation during embryonic development, but also in the maintenance of this repressive mark in proliferating cells. Consistent with this notion, EZH2 and NIPP1 silence a common set of genes, as revealed by gene-expression pro. ling, and NIPP1 is associated with established Polycomb target genes and with genomic regions that are enriched in Polycomb targets. Furthermore, most NIPP1 target genes are trimethylated on H3K27 and the knockdown of either NIPP1 or EZH2 is often associated with a loss of this modi. cation. Our data reveal that NIPP1 is required for the global trimethylation of H3K27 and is implicated in gene silencing by EZH2.
引用
收藏
页码:1449 / 1460
页数:12
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