11
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Polycomb group protein displacement and gene activation through MSK-dependent H3K27me3S28 phosphorylation.

      Molecular Cell
      Activating Transcription Factor 3, genetics, Anisomycin, pharmacology, Antibodies, immunology, Cell Differentiation, drug effects, Cell Line, Tumor, Chromatin, metabolism, DNA Damage, Embryonic Stem Cells, Fibroblasts, Gene Expression, Gene Expression Regulation, physiology, HeLa Cells, Histones, Humans, Lysine, Methylation, Mitosis, Neurons, cytology, Peptides, Phosphorylation, Polycomb-Group Proteins, Promoter Regions, Genetic, Protein Binding, Protein Transport, Repressor Proteins, Ribosomal Protein S6 Kinases, 90-kDa, antagonists & inhibitors, Serine

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Epigenetic regulation of chromatin structure is essential for the expression of genes determining cellular specification and function. The Polycomb repressive complex 2 (PRC2) di- and trimethylates histone H3 on lysine 27 (H3K27me2/me3) to establish repression of specific genes in embryonic stem cells and during differentiation. How the Polycomb group (PcG) target genes are regulated by environmental cues and signaling pathways is quite unexplored. Here, we show that the mitogen- and stress-activated kinases (MSK), through a mechanism that involves promoter recruitment, histone H3K27me3S28 phosphorylation, and displacement of PcG proteins, lead to gene activation. We present evidence that the H3K27me3S28 phosphorylation is functioning in response to stress signaling, mitogenic signaling, and retinoic acid (RA)-induced neuronal differentiation. We propose that MSK-mediated H3K27me3S28 phosphorylation serves as a mechanism to activate a subset of PcG target genes determined by the biological stimuli and thereby modulate the gene expression program determining cell fate. Copyright © 2010 Elsevier Inc. All rights reserved.

          Related collections

          Author and article information

          Comments

          Comment on this article