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Long non-coding RNA-polycomb intimate rendezvous

The interaction between polycomb-repressive complexes 1/2 (PRC1/2) and long non-coding RNA (lncRNA), such as the X inactive specific transcript Xist and the HOX transcript antisense RNA (HOTAIR), has been the subject of intense debate. While cross-linking, immuno-precipitation and super-resolution m...

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Detalles Bibliográficos
Autores principales: Cerase, Andrea, Tartaglia, Gian Gaetano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7536065/
https://www.ncbi.nlm.nih.gov/pubmed/32898472
http://dx.doi.org/10.1098/rsob.200126
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author Cerase, Andrea
Tartaglia, Gian Gaetano
author_facet Cerase, Andrea
Tartaglia, Gian Gaetano
author_sort Cerase, Andrea
collection PubMed
description The interaction between polycomb-repressive complexes 1/2 (PRC1/2) and long non-coding RNA (lncRNA), such as the X inactive specific transcript Xist and the HOX transcript antisense RNA (HOTAIR), has been the subject of intense debate. While cross-linking, immuno-precipitation and super-resolution microscopy argue against direct interaction of Polycomb with some lncRNAs, there is increasing evidence supporting the ability of both PRC1 and PRC2 to functionally associate with RNA. Recent data indicate that these interactions are in most cases spurious, but nonetheless crucial for a number of cellular activities. In this review, we suggest that while PRC1/2 recruitment by HOTAIR might be direct, in the case of Xist, it might occur indirectly and, at least in part, through the process of liquid–liquid phase separation. We present recent models of lncRNA-mediated PRC1/2 recruitment to their targets and describe potential RNA-mediated roles in the three-dimensional organization of the nucleus.
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spelling pubmed-75360652020-10-09 Long non-coding RNA-polycomb intimate rendezvous Cerase, Andrea Tartaglia, Gian Gaetano Open Biol Review The interaction between polycomb-repressive complexes 1/2 (PRC1/2) and long non-coding RNA (lncRNA), such as the X inactive specific transcript Xist and the HOX transcript antisense RNA (HOTAIR), has been the subject of intense debate. While cross-linking, immuno-precipitation and super-resolution microscopy argue against direct interaction of Polycomb with some lncRNAs, there is increasing evidence supporting the ability of both PRC1 and PRC2 to functionally associate with RNA. Recent data indicate that these interactions are in most cases spurious, but nonetheless crucial for a number of cellular activities. In this review, we suggest that while PRC1/2 recruitment by HOTAIR might be direct, in the case of Xist, it might occur indirectly and, at least in part, through the process of liquid–liquid phase separation. We present recent models of lncRNA-mediated PRC1/2 recruitment to their targets and describe potential RNA-mediated roles in the three-dimensional organization of the nucleus. The Royal Society 2020-09-09 /pmc/articles/PMC7536065/ /pubmed/32898472 http://dx.doi.org/10.1098/rsob.200126 Text en © 2020 The Authors. http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Review
Cerase, Andrea
Tartaglia, Gian Gaetano
Long non-coding RNA-polycomb intimate rendezvous
title Long non-coding RNA-polycomb intimate rendezvous
title_full Long non-coding RNA-polycomb intimate rendezvous
title_fullStr Long non-coding RNA-polycomb intimate rendezvous
title_full_unstemmed Long non-coding RNA-polycomb intimate rendezvous
title_short Long non-coding RNA-polycomb intimate rendezvous
title_sort long non-coding rna-polycomb intimate rendezvous
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7536065/
https://www.ncbi.nlm.nih.gov/pubmed/32898472
http://dx.doi.org/10.1098/rsob.200126
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