Polycomb Associates Genome-wide with a Specific RNA Polymerase II Variant, and Regulates Metabolic Genes in ESCs
Polycomb repressor complexes (PRCs) are important chromatin modifiers fundamentally implicated in pluripotency and cancer. Polycomb silencing in embryonic stem cells (ESCs) can be accompanied by active chromatin and primed RNA polymerase II (RNAPII), but the relationship between PRCs and RNAPII rema...
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2012
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Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3682187/ |
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pubmed-36821872013-06-19 Polycomb Associates Genome-wide with a Specific RNA Polymerase II Variant, and Regulates Metabolic Genes in ESCs Brookes, Emily de Santiago, Inês Hebenstreit, Daniel Morris, Kelly J. Carroll, Tom Xie, Sheila Q. Stock, Julie K. Heidemann, Martin Eick, Dirk Nozaki, Naohito Kimura, Hiroshi Ragoussis, Jiannis Teichmann, Sarah A. Pombo, Ana Article Polycomb repressor complexes (PRCs) are important chromatin modifiers fundamentally implicated in pluripotency and cancer. Polycomb silencing in embryonic stem cells (ESCs) can be accompanied by active chromatin and primed RNA polymerase II (RNAPII), but the relationship between PRCs and RNAPII remains unclear genome-wide. We mapped PRC repression markers and four RNAPII states in ESCs using ChIP-seq, and found that PRC targets exhibit a range of RNAPII variants. First, developmental PRC targets are bound by unproductive RNAPII (S5p+S7p−S2p−) genome-wide. Sequential ChIP, Ring1B depletion, and genome-wide correlations show that PRCs and RNAPII-S5p physically bind to the same chromatin and functionally synergize. Second, we identify a cohort of genes marked by PRC and elongating RNAPII (S5p+S7p+S2p+); they produce mRNA and protein, and their expression increases upon PRC1 knockdown. We show that this group of PRC targets switches between active and PRC-repressed states within the ESC population, and that many have roles in metabolism. Cell Press 2012-02-03 /pmc/articles/PMC3682187/ /pubmed/22305566 http://dx.doi.org/10.1016/j.stem.2011.12.017 Text en © 2012 ELL & Excerpta Medica. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license |
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Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
building |
NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Brookes, Emily de Santiago, Inês Hebenstreit, Daniel Morris, Kelly J. Carroll, Tom Xie, Sheila Q. Stock, Julie K. Heidemann, Martin Eick, Dirk Nozaki, Naohito Kimura, Hiroshi Ragoussis, Jiannis Teichmann, Sarah A. Pombo, Ana |
spellingShingle |
Brookes, Emily de Santiago, Inês Hebenstreit, Daniel Morris, Kelly J. Carroll, Tom Xie, Sheila Q. Stock, Julie K. Heidemann, Martin Eick, Dirk Nozaki, Naohito Kimura, Hiroshi Ragoussis, Jiannis Teichmann, Sarah A. Pombo, Ana Polycomb Associates Genome-wide with a Specific RNA Polymerase II Variant, and Regulates Metabolic Genes in ESCs |
author_facet |
Brookes, Emily de Santiago, Inês Hebenstreit, Daniel Morris, Kelly J. Carroll, Tom Xie, Sheila Q. Stock, Julie K. Heidemann, Martin Eick, Dirk Nozaki, Naohito Kimura, Hiroshi Ragoussis, Jiannis Teichmann, Sarah A. Pombo, Ana |
author_sort |
Brookes, Emily |
title |
Polycomb Associates Genome-wide with a Specific RNA Polymerase II Variant, and Regulates Metabolic Genes in ESCs |
title_short |
Polycomb Associates Genome-wide with a Specific RNA Polymerase II Variant, and Regulates Metabolic Genes in ESCs |
title_full |
Polycomb Associates Genome-wide with a Specific RNA Polymerase II Variant, and Regulates Metabolic Genes in ESCs |
title_fullStr |
Polycomb Associates Genome-wide with a Specific RNA Polymerase II Variant, and Regulates Metabolic Genes in ESCs |
title_full_unstemmed |
Polycomb Associates Genome-wide with a Specific RNA Polymerase II Variant, and Regulates Metabolic Genes in ESCs |
title_sort |
polycomb associates genome-wide with a specific rna polymerase ii variant, and regulates metabolic genes in escs |
description |
Polycomb repressor complexes (PRCs) are important chromatin modifiers fundamentally implicated in pluripotency and cancer. Polycomb silencing in embryonic stem cells (ESCs) can be accompanied by active chromatin and primed RNA polymerase II (RNAPII), but the relationship between PRCs and RNAPII remains unclear genome-wide. We mapped PRC repression markers and four RNAPII states in ESCs using ChIP-seq, and found that PRC targets exhibit a range of RNAPII variants. First, developmental PRC targets are bound by unproductive RNAPII (S5p+S7p−S2p−) genome-wide. Sequential ChIP, Ring1B depletion, and genome-wide correlations show that PRCs and RNAPII-S5p physically bind to the same chromatin and functionally synergize. Second, we identify a cohort of genes marked by PRC and elongating RNAPII (S5p+S7p+S2p+); they produce mRNA and protein, and their expression increases upon PRC1 knockdown. We show that this group of PRC targets switches between active and PRC-repressed states within the ESC population, and that many have roles in metabolism. |
publisher |
Cell Press |
publishDate |
2012 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3682187/ |
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1611986456945885184 |