| Literature DB >> 29628311 |
Eric Conway1, Emilia Jerman1, Evan Healy1, Shinsuke Ito2, Daniel Holoch3, Giorgio Oliviero4, Orla Deevy1, Eleanor Glancy1, Darren J Fitzpatrick1, Marlena Mucha1, Ariane Watson4, Alan M Rice1, Paul Chammas5, Christine Huang6, Indigo Pratt-Kelly1, Yoko Koseki2, Manabu Nakayama7, Tomoyuki Ishikura2, Gundula Streubel1, Kieran Wynne8, Karsten Hokamp1, Aoife McLysaght1, Claudio Ciferri7, Luciano Di Croce9, Gerard Cagney4, Raphaël Margueron3, Haruhiko Koseki2, Adrian P Bracken10.
Abstract
The polycomb repressive complex 2 (PRC2) consists of core subunits SUZ12, EED, RBBP4/7, and EZH1/2 and is responsible for mono-, di-, and tri-methylation of lysine 27 on histone H3. Whereas two distinct forms exist, PRC2.1 (containing one polycomb-like protein) and PRC2.2 (containing AEBP2 and JARID2), little is known about their differential functions. Here, we report the discovery of a family of vertebrate-specific PRC2.1 proteins, "PRC2 associated LCOR isoform 1" (PALI1) and PALI2, encoded by the LCOR and LCORL gene loci, respectively. PALI1 promotes PRC2 methyltransferase activity in vitro and in vivo and is essential for mouse development. Pali1 and Aebp2 define mutually exclusive, antagonistic PRC2 subtypes that exhibit divergent H3K27-tri-methylation activities. The balance of these PRC2.1/PRC2.2 activities is required for the appropriate regulation of polycomb target genes during differentiation. PALI1/2 potentially link polycombs with transcriptional co-repressors in the regulation of cellular identity during development and in cancer.Entities:
Keywords: AEBP2; C10ORF12; EZH2; H3K27me2; H3K27me3; LCOR; PALI1; PRC2; polycomb
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Year: 2018 PMID: 29628311 DOI: 10.1016/j.molcel.2018.03.005
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970