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Paraspeckles modulate the intranuclear distribution of paraspeckle-associated Ctn RNA
Paraspeckles are sub-nuclear domains that are nucleated by long noncoding RNA Neat1. While interaction of protein components of paraspeckles and Neat1 is understood, there is limited information on the interaction of non-structural RNA components with paraspeckles. Here, by varying paraspeckle numbe...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036046/ https://www.ncbi.nlm.nih.gov/pubmed/27665741 http://dx.doi.org/10.1038/srep34043 |
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author | Anantharaman, Aparna Jadaliha, Mahdieh Tripathi, Vidisha Nakagawa, Shinichi Hirose, Tetsuro Jantsch, Michael F. Prasanth, Supriya G. Prasanth, Kannanganattu V. |
author_facet | Anantharaman, Aparna Jadaliha, Mahdieh Tripathi, Vidisha Nakagawa, Shinichi Hirose, Tetsuro Jantsch, Michael F. Prasanth, Supriya G. Prasanth, Kannanganattu V. |
author_sort | Anantharaman, Aparna |
collection | PubMed |
description | Paraspeckles are sub-nuclear domains that are nucleated by long noncoding RNA Neat1. While interaction of protein components of paraspeckles and Neat1 is understood, there is limited information on the interaction of non-structural RNA components with paraspeckles. Here, by varying paraspeckle number and size, we investigate how paraspeckles influence the nuclear organization of their non-structural RNA component Ctn RNA. Our results show that Ctn RNA remains nuclear-retained in the absence of intact paraspeckles, suggesting that they do not regulate nuclear retention of Ctn RNA. In the absence of Neat1, Ctn RNA continues to interact with paraspeckle protein NonO to form residual nuclear foci. In addition, in the absence of Neat1-nucleated paraspeckles, a subset of Ctn RNA localizes to the perinucleolar regions. Concomitant with increase in number of paraspeckles, transcriptional reactivation resulted in increased number of paraspeckle-localized Ctn RNA foci. Similar to Neat1, proteasome inhibition altered the localization of Ctn RNA, where it formed enlarged paraspeckle-like foci. Super-resolution structured illumination microscopic analyses revealed that in paraspeckles, Ctn RNA partially co-localized with Neat1, and displayed a more heterogeneous intra-paraspeckle localization. Collectively, these results show that while paraspeckles do not influence nuclear retention of Ctn RNA, they modulate its intranuclear compartmentalization. |
format | Online Article Text |
id | pubmed-5036046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50360462016-09-30 Paraspeckles modulate the intranuclear distribution of paraspeckle-associated Ctn RNA Anantharaman, Aparna Jadaliha, Mahdieh Tripathi, Vidisha Nakagawa, Shinichi Hirose, Tetsuro Jantsch, Michael F. Prasanth, Supriya G. Prasanth, Kannanganattu V. Sci Rep Article Paraspeckles are sub-nuclear domains that are nucleated by long noncoding RNA Neat1. While interaction of protein components of paraspeckles and Neat1 is understood, there is limited information on the interaction of non-structural RNA components with paraspeckles. Here, by varying paraspeckle number and size, we investigate how paraspeckles influence the nuclear organization of their non-structural RNA component Ctn RNA. Our results show that Ctn RNA remains nuclear-retained in the absence of intact paraspeckles, suggesting that they do not regulate nuclear retention of Ctn RNA. In the absence of Neat1, Ctn RNA continues to interact with paraspeckle protein NonO to form residual nuclear foci. In addition, in the absence of Neat1-nucleated paraspeckles, a subset of Ctn RNA localizes to the perinucleolar regions. Concomitant with increase in number of paraspeckles, transcriptional reactivation resulted in increased number of paraspeckle-localized Ctn RNA foci. Similar to Neat1, proteasome inhibition altered the localization of Ctn RNA, where it formed enlarged paraspeckle-like foci. Super-resolution structured illumination microscopic analyses revealed that in paraspeckles, Ctn RNA partially co-localized with Neat1, and displayed a more heterogeneous intra-paraspeckle localization. Collectively, these results show that while paraspeckles do not influence nuclear retention of Ctn RNA, they modulate its intranuclear compartmentalization. Nature Publishing Group 2016-09-26 /pmc/articles/PMC5036046/ /pubmed/27665741 http://dx.doi.org/10.1038/srep34043 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Anantharaman, Aparna Jadaliha, Mahdieh Tripathi, Vidisha Nakagawa, Shinichi Hirose, Tetsuro Jantsch, Michael F. Prasanth, Supriya G. Prasanth, Kannanganattu V. Paraspeckles modulate the intranuclear distribution of paraspeckle-associated Ctn RNA |
title | Paraspeckles modulate the intranuclear distribution of paraspeckle-associated Ctn RNA |
title_full | Paraspeckles modulate the intranuclear distribution of paraspeckle-associated Ctn RNA |
title_fullStr | Paraspeckles modulate the intranuclear distribution of paraspeckle-associated Ctn RNA |
title_full_unstemmed | Paraspeckles modulate the intranuclear distribution of paraspeckle-associated Ctn RNA |
title_short | Paraspeckles modulate the intranuclear distribution of paraspeckle-associated Ctn RNA |
title_sort | paraspeckles modulate the intranuclear distribution of paraspeckle-associated ctn rna |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036046/ https://www.ncbi.nlm.nih.gov/pubmed/27665741 http://dx.doi.org/10.1038/srep34043 |
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