The recruitment of chromatin modifiers by long noncoding RNAs: lessons from PRC2

被引:237
作者
Davidovich, Chen
Cech, Thomas R.
机构
[1] Univ Colorado, BioFrontiers Inst, Boulder, CO 80309 USA
[2] Univ Colorado, Howard Hughes Med Inst, Boulder, CO 80309 USA
关键词
PRC2; RNA-protein interaction; epigenetic silencing; histone modification; long noncoding RNAs; REPRESSIVE COMPLEX 2; HISTONE METHYLTRANSFERASE ACTIVITY; H3; LYSINE-27; METHYLATION; DEAD-BOX PROTEIN; XIST RNA; GENE-EXPRESSION; RESTRICTION ENDONUCLEASE; TRANSCRIPTIONAL NOISE; BINDING-SPECIFICITY; WIDE IDENTIFICATION;
D O I
10.1261/rna.053918.115
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
Polycomb repressive complex-2 (PRC2) is a histone methyltransferase required for epigenetic silencing during development and cancer. Among chromatin modifying factors shown to be recruited and regulated by long noncoding RNAs (IncRNAs), PRC2 is one of the most studied. Mammalian PRC2 binds thousands of RNAs in vivo, and it is becoming a model system for the recruitment of chromatin modifying factors by RNA. Yet, well-defined PRC2-binding motifs within target RNAs have been elusive. From the protein side, PRC2 RNA-binding subunits contain no known RNA-binding domains, complicating functional studies. Here we provide a critical review of existing models for the recruitment of PRC2 to chromatin by RNAs. This discussion may also serve researchers who are studying the recruitment of other chromatin modifiers by IncRNAs.
引用
收藏
页码:2007 / 2022
页数:16
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