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Binding Interactions between Long Noncoding RNA HOTAIR and PRC2 Proteins
[Image: see text] Long noncoding RNAs (lncRNAs) play a key role in the epigenetic regulation of cells. Many of these lncRNAs function by interacting with histone repressive proteins of the Polycomb group (PcG) family, recruiting them to gene loci to facilitate silencing. Although there are now many...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3964825/ https://www.ncbi.nlm.nih.gov/pubmed/24320048 http://dx.doi.org/10.1021/bi401085h |
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author | Wu, Liang Murat, Pierre Matak-Vinkovic, Dijana Murrell, Adele Balasubramanian, Shankar |
author_facet | Wu, Liang Murat, Pierre Matak-Vinkovic, Dijana Murrell, Adele Balasubramanian, Shankar |
author_sort | Wu, Liang |
collection | PubMed |
description | [Image: see text] Long noncoding RNAs (lncRNAs) play a key role in the epigenetic regulation of cells. Many of these lncRNAs function by interacting with histone repressive proteins of the Polycomb group (PcG) family, recruiting them to gene loci to facilitate silencing. Although there are now many RNAs known to interact with the PRC2 complex, little is known about the details of the molecular interactions. Here, we show that the PcG protein heterodimer EZH2-EED is necessary and sufficient for binding to the lncRNA HOTAIR. We also show that protein recognition occurs within a folded 89-mer domain of HOTAIR. This 89-mer represents a minimal binding motif, as further deletion of nucleotides results in substantial loss of affinity for PRC2. These findings provide molecular insights into an important system involved in epigenetic regulation. |
format | Online Article Text |
id | pubmed-3964825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-39648252014-03-26 Binding Interactions between Long Noncoding RNA HOTAIR and PRC2 Proteins Wu, Liang Murat, Pierre Matak-Vinkovic, Dijana Murrell, Adele Balasubramanian, Shankar Biochemistry [Image: see text] Long noncoding RNAs (lncRNAs) play a key role in the epigenetic regulation of cells. Many of these lncRNAs function by interacting with histone repressive proteins of the Polycomb group (PcG) family, recruiting them to gene loci to facilitate silencing. Although there are now many RNAs known to interact with the PRC2 complex, little is known about the details of the molecular interactions. Here, we show that the PcG protein heterodimer EZH2-EED is necessary and sufficient for binding to the lncRNA HOTAIR. We also show that protein recognition occurs within a folded 89-mer domain of HOTAIR. This 89-mer represents a minimal binding motif, as further deletion of nucleotides results in substantial loss of affinity for PRC2. These findings provide molecular insights into an important system involved in epigenetic regulation. American Chemical Society 2013-12-10 2013-12-31 /pmc/articles/PMC3964825/ /pubmed/24320048 http://dx.doi.org/10.1021/bi401085h Text en Copyright © 2013 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) |
spellingShingle | Wu, Liang Murat, Pierre Matak-Vinkovic, Dijana Murrell, Adele Balasubramanian, Shankar Binding Interactions between Long Noncoding RNA HOTAIR and PRC2 Proteins |
title | Binding Interactions between Long Noncoding RNA HOTAIR
and PRC2 Proteins |
title_full | Binding Interactions between Long Noncoding RNA HOTAIR
and PRC2 Proteins |
title_fullStr | Binding Interactions between Long Noncoding RNA HOTAIR
and PRC2 Proteins |
title_full_unstemmed | Binding Interactions between Long Noncoding RNA HOTAIR
and PRC2 Proteins |
title_short | Binding Interactions between Long Noncoding RNA HOTAIR
and PRC2 Proteins |
title_sort | binding interactions between long noncoding rna hotair
and prc2 proteins |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3964825/ https://www.ncbi.nlm.nih.gov/pubmed/24320048 http://dx.doi.org/10.1021/bi401085h |
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