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Nascent RNA interaction keeps PRC2 activity poised and in check

Polycomb-repressive complex 2 (PRC2) facilitates the maintenance and inheritance of chromatin domains repressive to transcription through catalysis of methylation of histone H3 at Lys27 (H3K27me2/3). However, through its EZH2 subunit, PRC2 also binds to nascent transcripts from active genes that are...

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Detalles Bibliográficos
Autores principales: Kaneko, Syuzo, Son, Jinsook, Bonasio, Roberto, Shen, Steven S., Reinberg, Danny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173153/
https://www.ncbi.nlm.nih.gov/pubmed/25170018
http://dx.doi.org/10.1101/gad.247940.114
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author Kaneko, Syuzo
Son, Jinsook
Bonasio, Roberto
Shen, Steven S.
Reinberg, Danny
author_facet Kaneko, Syuzo
Son, Jinsook
Bonasio, Roberto
Shen, Steven S.
Reinberg, Danny
author_sort Kaneko, Syuzo
collection PubMed
description Polycomb-repressive complex 2 (PRC2) facilitates the maintenance and inheritance of chromatin domains repressive to transcription through catalysis of methylation of histone H3 at Lys27 (H3K27me2/3). However, through its EZH2 subunit, PRC2 also binds to nascent transcripts from active genes that are devoid of H3K27me2/3 in embryonic stem cells. Here, biochemical analyses indicated that RNA interaction inhibits SET domain-containing proteins, such as PRC2, nonspecifically in vitro. However, CRISPR-mediated truncation of a PRC2-interacting nascent RNA rescued PRC2-mediated deposition of H3K27me2/3. That PRC2 activity is inhibited by interactions with nascent transcripts supports a model in which PRC2 can only mark for repression those genes silenced by transcriptional repressors.
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spelling pubmed-41731532015-03-15 Nascent RNA interaction keeps PRC2 activity poised and in check Kaneko, Syuzo Son, Jinsook Bonasio, Roberto Shen, Steven S. Reinberg, Danny Genes Dev Research Communication Polycomb-repressive complex 2 (PRC2) facilitates the maintenance and inheritance of chromatin domains repressive to transcription through catalysis of methylation of histone H3 at Lys27 (H3K27me2/3). However, through its EZH2 subunit, PRC2 also binds to nascent transcripts from active genes that are devoid of H3K27me2/3 in embryonic stem cells. Here, biochemical analyses indicated that RNA interaction inhibits SET domain-containing proteins, such as PRC2, nonspecifically in vitro. However, CRISPR-mediated truncation of a PRC2-interacting nascent RNA rescued PRC2-mediated deposition of H3K27me2/3. That PRC2 activity is inhibited by interactions with nascent transcripts supports a model in which PRC2 can only mark for repression those genes silenced by transcriptional repressors. Cold Spring Harbor Laboratory Press 2014-09-15 /pmc/articles/PMC4173153/ /pubmed/25170018 http://dx.doi.org/10.1101/gad.247940.114 Text en © 2014 Kaneko et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Research Communication
Kaneko, Syuzo
Son, Jinsook
Bonasio, Roberto
Shen, Steven S.
Reinberg, Danny
Nascent RNA interaction keeps PRC2 activity poised and in check
title Nascent RNA interaction keeps PRC2 activity poised and in check
title_full Nascent RNA interaction keeps PRC2 activity poised and in check
title_fullStr Nascent RNA interaction keeps PRC2 activity poised and in check
title_full_unstemmed Nascent RNA interaction keeps PRC2 activity poised and in check
title_short Nascent RNA interaction keeps PRC2 activity poised and in check
title_sort nascent rna interaction keeps prc2 activity poised and in check
topic Research Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173153/
https://www.ncbi.nlm.nih.gov/pubmed/25170018
http://dx.doi.org/10.1101/gad.247940.114
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