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FISH-Flow to quantify nascent and mature ribosomal RNA in mouse and human cells

FISH-Flow (fluorescence in situ hybridization-flow cytometry) involves hybridizing fluorescent oligos to RNA and quantifying fluorescence at a single-cell level using flow cytometry. Here, we present a FISH-Flow protocol to quantify nascent 47S and mature 18S and 28S rRNAs in mouse and human cells,...

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Detalles Bibliográficos
Autores principales: Antony, Charles, Somers, Patrick, Gray, Erin M., Pimkin, Maxim, Paralkar, Vikram R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374870/
https://www.ncbi.nlm.nih.gov/pubmed/37481729
http://dx.doi.org/10.1016/j.xpro.2023.102463
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author Antony, Charles
Somers, Patrick
Gray, Erin M.
Pimkin, Maxim
Paralkar, Vikram R.
author_facet Antony, Charles
Somers, Patrick
Gray, Erin M.
Pimkin, Maxim
Paralkar, Vikram R.
author_sort Antony, Charles
collection PubMed
description FISH-Flow (fluorescence in situ hybridization-flow cytometry) involves hybridizing fluorescent oligos to RNA and quantifying fluorescence at a single-cell level using flow cytometry. Here, we present a FISH-Flow protocol to quantify nascent 47S and mature 18S and 28S rRNAs in mouse and human cells, including rRNA quantification across cell cycle stages using DNA staining. We describe steps for cell preparation, hybridization of fluorescent probes against rRNA, and DNA staining. We then detail procedures for flow cytometry and data analysis. For complete details on the use and execution of this protocol, please refer to Antony et al. (2022).(1)
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spelling pubmed-103748702023-07-29 FISH-Flow to quantify nascent and mature ribosomal RNA in mouse and human cells Antony, Charles Somers, Patrick Gray, Erin M. Pimkin, Maxim Paralkar, Vikram R. STAR Protoc Protocol FISH-Flow (fluorescence in situ hybridization-flow cytometry) involves hybridizing fluorescent oligos to RNA and quantifying fluorescence at a single-cell level using flow cytometry. Here, we present a FISH-Flow protocol to quantify nascent 47S and mature 18S and 28S rRNAs in mouse and human cells, including rRNA quantification across cell cycle stages using DNA staining. We describe steps for cell preparation, hybridization of fluorescent probes against rRNA, and DNA staining. We then detail procedures for flow cytometry and data analysis. For complete details on the use and execution of this protocol, please refer to Antony et al. (2022).(1) Elsevier 2023-07-22 /pmc/articles/PMC10374870/ /pubmed/37481729 http://dx.doi.org/10.1016/j.xpro.2023.102463 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Antony, Charles
Somers, Patrick
Gray, Erin M.
Pimkin, Maxim
Paralkar, Vikram R.
FISH-Flow to quantify nascent and mature ribosomal RNA in mouse and human cells
title FISH-Flow to quantify nascent and mature ribosomal RNA in mouse and human cells
title_full FISH-Flow to quantify nascent and mature ribosomal RNA in mouse and human cells
title_fullStr FISH-Flow to quantify nascent and mature ribosomal RNA in mouse and human cells
title_full_unstemmed FISH-Flow to quantify nascent and mature ribosomal RNA in mouse and human cells
title_short FISH-Flow to quantify nascent and mature ribosomal RNA in mouse and human cells
title_sort fish-flow to quantify nascent and mature ribosomal rna in mouse and human cells
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374870/
https://www.ncbi.nlm.nih.gov/pubmed/37481729
http://dx.doi.org/10.1016/j.xpro.2023.102463
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