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The recruitment of chromatin modifiers by long noncoding RNAs: lessons from PRC2

Polycomb repressive complex-2 (PRC2) is a histone methyltransferase required for epigenetic silencing during development and cancer. Among chromatin modifying factors shown to be recruited and regulated by long noncoding RNAs (lncRNAs), PRC2 is one of the most studied. Mammalian PRC2 binds thousands...

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Detalles Bibliográficos
Autores principales: Davidovich, Chen, Cech, Thomas R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4647455/
https://www.ncbi.nlm.nih.gov/pubmed/26574518
http://dx.doi.org/10.1261/rna.053918.115
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author Davidovich, Chen
Cech, Thomas R.
author_facet Davidovich, Chen
Cech, Thomas R.
author_sort Davidovich, Chen
collection PubMed
description Polycomb repressive complex-2 (PRC2) is a histone methyltransferase required for epigenetic silencing during development and cancer. Among chromatin modifying factors shown to be recruited and regulated by long noncoding RNAs (lncRNAs), PRC2 is one of the most studied. Mammalian PRC2 binds thousands of RNAs in vivo, and it is becoming a model system for the recruitment of chromatin modifying factors by RNA. Yet, well-defined PRC2-binding motifs within target RNAs have been elusive. From the protein side, PRC2 RNA-binding subunits contain no known RNA-binding domains, complicating functional studies. Here we provide a critical review of existing models for the recruitment of PRC2 to chromatin by RNAs. This discussion may also serve researchers who are studying the recruitment of other chromatin modifiers by lncRNAs.
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spelling pubmed-46474552016-12-01 The recruitment of chromatin modifiers by long noncoding RNAs: lessons from PRC2 Davidovich, Chen Cech, Thomas R. RNA Review Polycomb repressive complex-2 (PRC2) is a histone methyltransferase required for epigenetic silencing during development and cancer. Among chromatin modifying factors shown to be recruited and regulated by long noncoding RNAs (lncRNAs), PRC2 is one of the most studied. Mammalian PRC2 binds thousands of RNAs in vivo, and it is becoming a model system for the recruitment of chromatin modifying factors by RNA. Yet, well-defined PRC2-binding motifs within target RNAs have been elusive. From the protein side, PRC2 RNA-binding subunits contain no known RNA-binding domains, complicating functional studies. Here we provide a critical review of existing models for the recruitment of PRC2 to chromatin by RNAs. This discussion may also serve researchers who are studying the recruitment of other chromatin modifiers by lncRNAs. Cold Spring Harbor Laboratory Press 2015-12 /pmc/articles/PMC4647455/ /pubmed/26574518 http://dx.doi.org/10.1261/rna.053918.115 Text en © 2015 Davidovich and Cech; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 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 Review
Davidovich, Chen
Cech, Thomas R.
The recruitment of chromatin modifiers by long noncoding RNAs: lessons from PRC2
title The recruitment of chromatin modifiers by long noncoding RNAs: lessons from PRC2
title_full The recruitment of chromatin modifiers by long noncoding RNAs: lessons from PRC2
title_fullStr The recruitment of chromatin modifiers by long noncoding RNAs: lessons from PRC2
title_full_unstemmed The recruitment of chromatin modifiers by long noncoding RNAs: lessons from PRC2
title_short The recruitment of chromatin modifiers by long noncoding RNAs: lessons from PRC2
title_sort recruitment of chromatin modifiers by long noncoding rnas: lessons from prc2
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4647455/
https://www.ncbi.nlm.nih.gov/pubmed/26574518
http://dx.doi.org/10.1261/rna.053918.115
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