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Structural, super-resolution microscopy analysis of paraspeckle nuclear body organization
Paraspeckles are nuclear bodies built on the long noncoding RNA Neat1, which regulates a variety of physiological processes including cancer progression and corpus luteum formation. To obtain further insight into the molecular basis of the function of paraspeckles, we performed fine structural analy...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037409/ https://www.ncbi.nlm.nih.gov/pubmed/27646274 http://dx.doi.org/10.1083/jcb.201601071 |
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author | West, Jason A. Mito, Mari Kurosaka, Satoshi Takumi, Toru Tanegashima, Chiharu Chujo, Takeshi Yanaka, Kaori Kingston, Robert E. Hirose, Tetsuro Bond, Charles Fox, Archa Nakagawa, Shinichi |
author_facet | West, Jason A. Mito, Mari Kurosaka, Satoshi Takumi, Toru Tanegashima, Chiharu Chujo, Takeshi Yanaka, Kaori Kingston, Robert E. Hirose, Tetsuro Bond, Charles Fox, Archa Nakagawa, Shinichi |
author_sort | West, Jason A. |
collection | PubMed |
description | Paraspeckles are nuclear bodies built on the long noncoding RNA Neat1, which regulates a variety of physiological processes including cancer progression and corpus luteum formation. To obtain further insight into the molecular basis of the function of paraspeckles, we performed fine structural analyses of these nuclear bodies using structural illumination microscopy. Notably, paraspeckle proteins are found within different layers along the radially arranged bundles of Neat1 transcripts, forming a characteristic core-shell spheroidal structure. In cells lacking the RNA binding protein Fus, paraspeckle spheroids are disassembled into smaller particles containing Neat1, which are diffusely distributed in the nucleoplasm. Sequencing analysis of RNAs purified from paraspeckles revealed that AG-rich transcripts associate with Neat1, which are distributed along the shell of the paraspeckle spheroids. We propose that paraspeckles sequester core components inside the spheroids, whereas the outer surface associates with other components in the nucleoplasm to fulfill their function. |
format | Online Article Text |
id | pubmed-5037409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50374092017-03-26 Structural, super-resolution microscopy analysis of paraspeckle nuclear body organization West, Jason A. Mito, Mari Kurosaka, Satoshi Takumi, Toru Tanegashima, Chiharu Chujo, Takeshi Yanaka, Kaori Kingston, Robert E. Hirose, Tetsuro Bond, Charles Fox, Archa Nakagawa, Shinichi J Cell Biol Research Articles Paraspeckles are nuclear bodies built on the long noncoding RNA Neat1, which regulates a variety of physiological processes including cancer progression and corpus luteum formation. To obtain further insight into the molecular basis of the function of paraspeckles, we performed fine structural analyses of these nuclear bodies using structural illumination microscopy. Notably, paraspeckle proteins are found within different layers along the radially arranged bundles of Neat1 transcripts, forming a characteristic core-shell spheroidal structure. In cells lacking the RNA binding protein Fus, paraspeckle spheroids are disassembled into smaller particles containing Neat1, which are diffusely distributed in the nucleoplasm. Sequencing analysis of RNAs purified from paraspeckles revealed that AG-rich transcripts associate with Neat1, which are distributed along the shell of the paraspeckle spheroids. We propose that paraspeckles sequester core components inside the spheroids, whereas the outer surface associates with other components in the nucleoplasm to fulfill their function. The Rockefeller University Press 2016-09-26 /pmc/articles/PMC5037409/ /pubmed/27646274 http://dx.doi.org/10.1083/jcb.201601071 Text en © 2016 West et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles West, Jason A. Mito, Mari Kurosaka, Satoshi Takumi, Toru Tanegashima, Chiharu Chujo, Takeshi Yanaka, Kaori Kingston, Robert E. Hirose, Tetsuro Bond, Charles Fox, Archa Nakagawa, Shinichi Structural, super-resolution microscopy analysis of paraspeckle nuclear body organization |
title | Structural, super-resolution microscopy analysis of paraspeckle nuclear body organization |
title_full | Structural, super-resolution microscopy analysis of paraspeckle nuclear body organization |
title_fullStr | Structural, super-resolution microscopy analysis of paraspeckle nuclear body organization |
title_full_unstemmed | Structural, super-resolution microscopy analysis of paraspeckle nuclear body organization |
title_short | Structural, super-resolution microscopy analysis of paraspeckle nuclear body organization |
title_sort | structural, super-resolution microscopy analysis of paraspeckle nuclear body organization |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037409/ https://www.ncbi.nlm.nih.gov/pubmed/27646274 http://dx.doi.org/10.1083/jcb.201601071 |
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