Polycomb Protein Ezh1 Promotes RNA Polymerase II Elongation

• Published in: Molecular cell Vol. 45; no. 2; pp. 255 - 262
• Main Authors: Mousavi, Kambiz, Zare, Hossein, Wang, A. Hongjun, Sartorelli, Vittorio
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 27-01-2012
• Subjects: Animals; Cell Differentiation; chromatin; DNA-Binding Proteins - antagonists & inhibitors; DNA-Binding Proteins - genetics; DNA-Binding Proteins - metabolism; DNA-Binding Proteins - physiology; DNA-directed RNA polymerase; Epigenesis, Genetic; epigenetics; gene activation; gene expression; genes; Histone-Lysine N-Methyltransferase - antagonists & inhibitors; Histone-Lysine N-Methyltransferase - genetics; Histone-Lysine N-Methyltransferase - metabolism; Histone-Lysine N-Methyltransferase - physiology; histones; Histones - metabolism; lysine; mammals; messenger RNA; Methylation; Mice; Muscle Development; myocytes; occupancy; Peptide Chain Elongation, Translational - physiology; Polycomb Repressive Complex 2; proteins; Repressor Proteins - metabolism; RNA Interference; RNA Polymerase II - metabolism; RNA Polymerase II - physiology; skeletal muscle; transcription (genetics); Transcription Factors - antagonists & inhibitors; Transcription Factors - genetics; Transcription Factors - metabolism; Transcription Factors - physiology; transcriptional activation
• ISSN: 1097-2765; 1097-4164
• DOI: 10.1016/j.molcel.2011.11.019

Polycomb group (PcG) proteins initiate the formation of repressed chromatin domains and regulate developmental gene expression. A mammalian PcG protein, enhancer of zeste homolog 2 (Ezh2), triggers transcriptional repression by catalyzing the addition of methyl groups onto lysine 27 of histone H3 (H3K27me2/3). This action facilitates the binding of other PcG proteins to chromatin for purposes of transcriptional silencing. Interestingly, there exists a paralog of Ezh2, termed Ezh1, whose primary function remains unclear. Here, we provide evidence for genome-wide association of Ezh1 complex with active epigenetic mark (H3K4me3), RNA polymerase II (Pol II), and mRNA production. Ezh1 depletion reduced global Pol II occupancy within gene bodies and resulted in delayed transcriptional activation during differentiation of skeletal muscle cells. Conversely, overexpression of wild-type Ezh1 led to premature gene activation and rescued Pol II occupancy defects in Ezh1-depleted cells. Collectively, these findings reveal a role for a PcG complex in promoting mRNA transcription.
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► The majority of Ezh1-occupied genes are devoid of repressed H3K27me3+ chromatin domains ► Ezh1 occupies H3K4me3+ genes ► The majority of genes occupied by Ezh1 are transcriptionally active ► Ezh1 promotes RNA polymerase II elongation genome-wide