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Visualizing adenosine to inosine RNA editing in single mammalian cells
Conversion of adenosine to inosine is a frequent type of RNA editing, but important details about its biology remain unknown due to a lack of imaging tools. We developed inoFISH to directly visualize and quantify adenosine-to-inosine edited transcripts in situ. We found that editing of GRIA2, EIF2AK...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5542810/ https://www.ncbi.nlm.nih.gov/pubmed/28604724 http://dx.doi.org/10.1038/nmeth.4332 |
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author | Mellis, Ian A. Gupte, Rohit Raj, Arjun Rouhanifard, Sara H. |
author_facet | Mellis, Ian A. Gupte, Rohit Raj, Arjun Rouhanifard, Sara H. |
author_sort | Mellis, Ian A. |
collection | PubMed |
description | Conversion of adenosine to inosine is a frequent type of RNA editing, but important details about its biology remain unknown due to a lack of imaging tools. We developed inoFISH to directly visualize and quantify adenosine-to-inosine edited transcripts in situ. We found that editing of GRIA2, EIF2AK2, and NUP43 is uncorrelated with nuclear localization and paraspeckle association. Further, NUP43 exhibits constant editing levels between single cells while GRIA2 levels vary. |
format | Online Article Text |
id | pubmed-5542810 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
record_format | MEDLINE/PubMed |
spelling | pubmed-55428102017-12-12 Visualizing adenosine to inosine RNA editing in single mammalian cells Mellis, Ian A. Gupte, Rohit Raj, Arjun Rouhanifard, Sara H. Nat Methods Article Conversion of adenosine to inosine is a frequent type of RNA editing, but important details about its biology remain unknown due to a lack of imaging tools. We developed inoFISH to directly visualize and quantify adenosine-to-inosine edited transcripts in situ. We found that editing of GRIA2, EIF2AK2, and NUP43 is uncorrelated with nuclear localization and paraspeckle association. Further, NUP43 exhibits constant editing levels between single cells while GRIA2 levels vary. 2017-06-12 2017-08 /pmc/articles/PMC5542810/ /pubmed/28604724 http://dx.doi.org/10.1038/nmeth.4332 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Mellis, Ian A. Gupte, Rohit Raj, Arjun Rouhanifard, Sara H. Visualizing adenosine to inosine RNA editing in single mammalian cells |
title | Visualizing adenosine to inosine RNA editing in single mammalian cells |
title_full | Visualizing adenosine to inosine RNA editing in single mammalian cells |
title_fullStr | Visualizing adenosine to inosine RNA editing in single mammalian cells |
title_full_unstemmed | Visualizing adenosine to inosine RNA editing in single mammalian cells |
title_short | Visualizing adenosine to inosine RNA editing in single mammalian cells |
title_sort | visualizing adenosine to inosine rna editing in single mammalian cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5542810/ https://www.ncbi.nlm.nih.gov/pubmed/28604724 http://dx.doi.org/10.1038/nmeth.4332 |
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