| Literature DB >> 27405765 |
Mridula K Ray1, Ole Wiskow2, Matthew J King3, Nidha Ismail3, Ayla Ergun4, Yanqun Wang1, Aaron J Plys1, Christopher P Davis1, Katie Kathrein5, Ruslan Sadreyev4, Mark L Borowsky1, Kevin Eggan6, Leonard Zon5, Jenna L Galloway7, Robert E Kingston8.
Abstract
The essential functions of polycomb repressive complex 1 (PRC1) in development and gene silencing are thought to involve long non-coding RNAs (lncRNAs), but few specific lncRNAs that guide PRC1 activity are known. We screened for lncRNAs, which co-precipitate with PRC1 from chromatin and found candidates that impact polycomb group protein (PcG)-regulated gene expression in vivo A novel lncRNA from this screen, CAT7, regulates expression and polycomb group binding at the MNX1 locus during early neuronal differentiation. CAT7 contains a unique tandem repeat domain that shares high sequence similarity to a non-syntenic zebrafish analog, cat7l Defects caused by interference of cat7l RNA during zebrafish embryogenesis were rescued by human CAT7 RNA, enhanced by interference of a PRC1 component, and suppressed by interference of a known PRC1 target gene, demonstrating cat7l genetically interacts with a PRC1. We propose a model whereby PRC1 acts in concert with specific lncRNAs and that CAT7/cat7l represents convergent lncRNAs that independently evolved to tune PRC1 repression at individual loci.Entities:
Keywords: CsCl density gradient; PRC1; chromatin; chromatin regulation; development; gene expression; long noncoding RNA (long ncRNA, lncRNA); mammal; polycomb; zebrafish
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Year: 2016 PMID: 27405765 PMCID: PMC5016691 DOI: 10.1074/jbc.M116.730853
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157