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Disruption of an RNA-binding hinge region abolishes LHP1-mediated epigenetic repression

Epigenetic maintenance of gene repression is essential for development. Polycomb complexes are central to this memory, but many aspects of the underlying mechanism remain unclear. LIKE HETEROCHROMATIN PROTEIN 1 (LHP1) binds Polycomb-deposited H3K27me3 and is required for repression of many Polycomb...

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Autores principales: Berry, Scott, Rosa, Stefanie, Howard, Martin, Bühler, Marc, Dean, Caroline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5749160/
https://www.ncbi.nlm.nih.gov/pubmed/29212661
http://dx.doi.org/10.1101/gad.305227.117
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author Berry, Scott
Rosa, Stefanie
Howard, Martin
Bühler, Marc
Dean, Caroline
author_facet Berry, Scott
Rosa, Stefanie
Howard, Martin
Bühler, Marc
Dean, Caroline
author_sort Berry, Scott
collection PubMed
description Epigenetic maintenance of gene repression is essential for development. Polycomb complexes are central to this memory, but many aspects of the underlying mechanism remain unclear. LIKE HETEROCHROMATIN PROTEIN 1 (LHP1) binds Polycomb-deposited H3K27me3 and is required for repression of many Polycomb target genes in Arabidopsis. Here we show that LHP1 binds RNA in vitro through the intrinsically disordered hinge region. By independently perturbing the RNA-binding hinge region and H3K27me3 (trimethylation of histone H3 at Lys27) recognition, we found that both facilitate LHP1 localization and H3K27me3 maintenance. Disruption of the RNA-binding hinge region also prevented formation of subnuclear foci, structures potentially important for epigenetic repression.
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spelling pubmed-57491602018-01-19 Disruption of an RNA-binding hinge region abolishes LHP1-mediated epigenetic repression Berry, Scott Rosa, Stefanie Howard, Martin Bühler, Marc Dean, Caroline Genes Dev Research Communication Epigenetic maintenance of gene repression is essential for development. Polycomb complexes are central to this memory, but many aspects of the underlying mechanism remain unclear. LIKE HETEROCHROMATIN PROTEIN 1 (LHP1) binds Polycomb-deposited H3K27me3 and is required for repression of many Polycomb target genes in Arabidopsis. Here we show that LHP1 binds RNA in vitro through the intrinsically disordered hinge region. By independently perturbing the RNA-binding hinge region and H3K27me3 (trimethylation of histone H3 at Lys27) recognition, we found that both facilitate LHP1 localization and H3K27me3 maintenance. Disruption of the RNA-binding hinge region also prevented formation of subnuclear foci, structures potentially important for epigenetic repression. Cold Spring Harbor Laboratory Press 2017-11-01 /pmc/articles/PMC5749160/ /pubmed/29212661 http://dx.doi.org/10.1101/gad.305227.117 Text en © 2017 Berry et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by/4.0/ This article, published in Genes & Development, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Communication
Berry, Scott
Rosa, Stefanie
Howard, Martin
Bühler, Marc
Dean, Caroline
Disruption of an RNA-binding hinge region abolishes LHP1-mediated epigenetic repression
title Disruption of an RNA-binding hinge region abolishes LHP1-mediated epigenetic repression
title_full Disruption of an RNA-binding hinge region abolishes LHP1-mediated epigenetic repression
title_fullStr Disruption of an RNA-binding hinge region abolishes LHP1-mediated epigenetic repression
title_full_unstemmed Disruption of an RNA-binding hinge region abolishes LHP1-mediated epigenetic repression
title_short Disruption of an RNA-binding hinge region abolishes LHP1-mediated epigenetic repression
title_sort disruption of an rna-binding hinge region abolishes lhp1-mediated epigenetic repression
topic Research Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5749160/
https://www.ncbi.nlm.nih.gov/pubmed/29212661
http://dx.doi.org/10.1101/gad.305227.117
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