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Morphine leads to global genome changes in H3K27me3 levels via a Polycomb Repressive Complex 2 (PRC2) self-regulatory mechanism in mESCs.

Iraia Muñoa-HoyosJohn A HalsallManu AraolazaCarl WardIdoia GarciaItziar Urizar-ArenazaMarta GianzoPaloma GarciaBryan TurnerNerea Subiran
Published in: Clinical epigenetics (2020)
Morphine induces targeting of the PRC2 complex to selected promoters, including those of PRC2 components, leading to characteristic changes in gene expression and a global reduction in H3K27me3. Following morphine removal, enhanced promoter H3K27me3 levels revert to normal sooner than global H3K27me3 or PRC2 component transcript levels. We suggest that H3K27me3 is involved in initiating morphine-induced changes in gene expression, but not in their maintenance. Model of Polycomb repressive complex 2 (PRC2) and H3K27me3 alterations induced by chronic morphine exposure. Morphine induces H3K27me3 enrichment at promoters of genes encoding core members of the PRC2 complex and is associated with their transcriptional downregulation.
Keyphrases
  • gene expression
  • dna methylation
  • transcription factor
  • genome wide
  • signaling pathway
  • cancer therapy
  • heat shock
  • bioinformatics analysis