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Diverse activities of viral cis-acting RNA regulatory elements revealed using multicolor, long-term, single-cell imaging
Cis-acting RNA structural elements govern crucial aspects of viral gene expression. How these structures and other posttranscriptional signals affect RNA trafficking and translation in the context of single cells is poorly understood. Herein we describe a multicolor, long-term (>24 h) imaging str...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341730/ https://www.ncbi.nlm.nih.gov/pubmed/27903772 http://dx.doi.org/10.1091/mbc.E16-08-0612 |
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author | Pocock, Ginger M. Zimdars, Laraine L. Yuan, Ming Eliceiri, Kevin W. Ahlquist, Paul Sherer, Nathan M. |
author_facet | Pocock, Ginger M. Zimdars, Laraine L. Yuan, Ming Eliceiri, Kevin W. Ahlquist, Paul Sherer, Nathan M. |
author_sort | Pocock, Ginger M. |
collection | PubMed |
description | Cis-acting RNA structural elements govern crucial aspects of viral gene expression. How these structures and other posttranscriptional signals affect RNA trafficking and translation in the context of single cells is poorly understood. Herein we describe a multicolor, long-term (>24 h) imaging strategy for measuring integrated aspects of viral RNA regulatory control in individual cells. We apply this strategy to demonstrate differential mRNA trafficking behaviors governed by RNA elements derived from three retroviruses (HIV-1, murine leukemia virus, and Mason-Pfizer monkey virus), two hepadnaviruses (hepatitis B virus and woodchuck hepatitis virus), and an intron-retaining transcript encoded by the cellular NXF1 gene. Striking behaviors include “burst” RNA nuclear export dynamics regulated by HIV-1’s Rev response element and the viral Rev protein; transient aggregations of RNAs into discrete foci at or near the nuclear membrane triggered by multiple elements; and a novel, pulsiform RNA export activity regulated by the hepadnaviral posttranscriptional regulatory element. We incorporate single-cell tracking and a data-mining algorithm into our approach to obtain RNA element–specific, high-resolution gene expression signatures. Together these imaging assays constitute a tractable, systems-based platform for studying otherwise difficult to access spatiotemporal features of viral and cellular gene regulation. |
format | Online Article Text |
id | pubmed-5341730 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-53417302017-04-16 Diverse activities of viral cis-acting RNA regulatory elements revealed using multicolor, long-term, single-cell imaging Pocock, Ginger M. Zimdars, Laraine L. Yuan, Ming Eliceiri, Kevin W. Ahlquist, Paul Sherer, Nathan M. Mol Biol Cell Articles Cis-acting RNA structural elements govern crucial aspects of viral gene expression. How these structures and other posttranscriptional signals affect RNA trafficking and translation in the context of single cells is poorly understood. Herein we describe a multicolor, long-term (>24 h) imaging strategy for measuring integrated aspects of viral RNA regulatory control in individual cells. We apply this strategy to demonstrate differential mRNA trafficking behaviors governed by RNA elements derived from three retroviruses (HIV-1, murine leukemia virus, and Mason-Pfizer monkey virus), two hepadnaviruses (hepatitis B virus and woodchuck hepatitis virus), and an intron-retaining transcript encoded by the cellular NXF1 gene. Striking behaviors include “burst” RNA nuclear export dynamics regulated by HIV-1’s Rev response element and the viral Rev protein; transient aggregations of RNAs into discrete foci at or near the nuclear membrane triggered by multiple elements; and a novel, pulsiform RNA export activity regulated by the hepadnaviral posttranscriptional regulatory element. We incorporate single-cell tracking and a data-mining algorithm into our approach to obtain RNA element–specific, high-resolution gene expression signatures. Together these imaging assays constitute a tractable, systems-based platform for studying otherwise difficult to access spatiotemporal features of viral and cellular gene regulation. The American Society for Cell Biology 2017-02-01 /pmc/articles/PMC5341730/ /pubmed/27903772 http://dx.doi.org/10.1091/mbc.E16-08-0612 Text en © 2017 Pocock et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. |
spellingShingle | Articles Pocock, Ginger M. Zimdars, Laraine L. Yuan, Ming Eliceiri, Kevin W. Ahlquist, Paul Sherer, Nathan M. Diverse activities of viral cis-acting RNA regulatory elements revealed using multicolor, long-term, single-cell imaging |
title | Diverse activities of viral cis-acting RNA regulatory elements revealed using multicolor, long-term, single-cell imaging |
title_full | Diverse activities of viral cis-acting RNA regulatory elements revealed using multicolor, long-term, single-cell imaging |
title_fullStr | Diverse activities of viral cis-acting RNA regulatory elements revealed using multicolor, long-term, single-cell imaging |
title_full_unstemmed | Diverse activities of viral cis-acting RNA regulatory elements revealed using multicolor, long-term, single-cell imaging |
title_short | Diverse activities of viral cis-acting RNA regulatory elements revealed using multicolor, long-term, single-cell imaging |
title_sort | diverse activities of viral cis-acting rna regulatory elements revealed using multicolor, long-term, single-cell imaging |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341730/ https://www.ncbi.nlm.nih.gov/pubmed/27903772 http://dx.doi.org/10.1091/mbc.E16-08-0612 |
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