| Literature DB >> 28746865 |
Georgina Berrozpe1, Gene O Bryant1, Katherine Warpinski1, Dan Spagna1, Santosh Narayan1, Shivangi Shah1, Mark Ptashne2.
Abstract
How is Polycomb (Pc), a eukaryotic negative regulator of transcription, targeted to specific mammalian genes? Our genome-wide analysis of the Pc mark H3K27me3 in murine cells revealed that Pc is preferentially associated with CpG island promoters of genes that are transcribed at a low level and less so with promoters of genes that are either silent or more highly expressed. Studies of the CpG island promoter of the Kit gene demonstrate that Pc is largely absent when the gene is silent in myeloid cells, as well as when the gene is highly expressed in mast cells. Manipulations that increase transcription in the former case, and reduce it in the latter, increase Pc occupancy. The average negative effect of Pc, we infer, is about 2-fold. We suggest possible biological roles for such negative effects and propose a mechanism by which Pc might be recruited to weakly transcribed genes.Entities:
Keywords: CRISPR; CpG island promoters; Kit gene; Polycomb; enhancers; genome-wide; shRAD21; transcription
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Year: 2017 PMID: 28746865 PMCID: PMC5635825 DOI: 10.1016/j.celrep.2017.06.076
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423