Polycomb domain formation depends on short and long distance regulatory cues.

BACKGROUND: Polycomb group (PcG) proteins dynamically define cellular identities through the epigenetic repression of key developmental genes. In Drosophila, cis-regulatory regions termed PcG response elements (PREs) act as nucleation sites for PcG proteins to create large repressive PcG domains tha...

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Main Authors: Bernd Schuettengruber, Giacomo Cavalli
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3577894?pdf=render
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author Bernd Schuettengruber
Giacomo Cavalli
author_facet Bernd Schuettengruber
Giacomo Cavalli
author_sort Bernd Schuettengruber
collection DOAJ
description BACKGROUND: Polycomb group (PcG) proteins dynamically define cellular identities through the epigenetic repression of key developmental genes. In Drosophila, cis-regulatory regions termed PcG response elements (PREs) act as nucleation sites for PcG proteins to create large repressive PcG domains that are marked by trimethylation of lysine 27 on histone H3 (H3K27me3). In addition to an action in cis, PREs can interact over long distances, thereby enhancing PcG dependent silencing. How PcG domains are established, which factors limit their propagation in cis, and how long range interactions of PREs in trans affect the chromatin structure is largely unknown. PRINCIPAL FINDINGS: We demonstrate that the insertion of a PRE-containing transgene in the Drosophila genome generates an artificial PcG domain and we analyze its organization by quantitative ChIP and ChIP-on-chip experiments. Intriguingly, a boundary element and known insulator proteins do not necessarily interfere with spreading of H3K27me3. Instead, domain borders correlate with the presence of promoter regions bound by RNA Polymerase II and active chromatin marks. In contrast, genes that are silent during early fly development get included within the PcG domain and this incorporation interferes with gene activation at later developmental stages. Moreover, trans-interaction of the transgenic PRE with its homologous endogenous PRE results in increased PcG binding, correlating with reinforced silencing of genes within the domain borders. CONCLUSIONS: Our results suggest that higher-order organization of PcG-bound chromatin can stabilize gene silencing within PcG domains. Further we propose that multi-protein complexes associated with active promoters are able to define the limits of PcG domains. Future work aimed to pinpoint the factors providing this barrier function will be required to understand the precise molecular mechanism by which active promoter regions can act as boundaries to stop spreading of H3K27me3.
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spelling doaj.art-46c50a12a9df4692b3225b79e8ddf6f42022-12-22T02:31:47ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0182e5653110.1371/journal.pone.0056531Polycomb domain formation depends on short and long distance regulatory cues.Bernd SchuettengruberGiacomo CavalliBACKGROUND: Polycomb group (PcG) proteins dynamically define cellular identities through the epigenetic repression of key developmental genes. In Drosophila, cis-regulatory regions termed PcG response elements (PREs) act as nucleation sites for PcG proteins to create large repressive PcG domains that are marked by trimethylation of lysine 27 on histone H3 (H3K27me3). In addition to an action in cis, PREs can interact over long distances, thereby enhancing PcG dependent silencing. How PcG domains are established, which factors limit their propagation in cis, and how long range interactions of PREs in trans affect the chromatin structure is largely unknown. PRINCIPAL FINDINGS: We demonstrate that the insertion of a PRE-containing transgene in the Drosophila genome generates an artificial PcG domain and we analyze its organization by quantitative ChIP and ChIP-on-chip experiments. Intriguingly, a boundary element and known insulator proteins do not necessarily interfere with spreading of H3K27me3. Instead, domain borders correlate with the presence of promoter regions bound by RNA Polymerase II and active chromatin marks. In contrast, genes that are silent during early fly development get included within the PcG domain and this incorporation interferes with gene activation at later developmental stages. Moreover, trans-interaction of the transgenic PRE with its homologous endogenous PRE results in increased PcG binding, correlating with reinforced silencing of genes within the domain borders. CONCLUSIONS: Our results suggest that higher-order organization of PcG-bound chromatin can stabilize gene silencing within PcG domains. Further we propose that multi-protein complexes associated with active promoters are able to define the limits of PcG domains. Future work aimed to pinpoint the factors providing this barrier function will be required to understand the precise molecular mechanism by which active promoter regions can act as boundaries to stop spreading of H3K27me3.http://europepmc.org/articles/PMC3577894?pdf=render
spellingShingle Bernd Schuettengruber
Giacomo Cavalli
Polycomb domain formation depends on short and long distance regulatory cues.
PLoS ONE
title Polycomb domain formation depends on short and long distance regulatory cues.
title_full Polycomb domain formation depends on short and long distance regulatory cues.
title_fullStr Polycomb domain formation depends on short and long distance regulatory cues.
title_full_unstemmed Polycomb domain formation depends on short and long distance regulatory cues.
title_short Polycomb domain formation depends on short and long distance regulatory cues.
title_sort polycomb domain formation depends on short and long distance regulatory cues
url http://europepmc.org/articles/PMC3577894?pdf=render
work_keys_str_mv AT berndschuettengruber polycombdomainformationdependsonshortandlongdistanceregulatorycues
AT giacomocavalli polycombdomainformationdependsonshortandlongdistanceregulatorycues