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mRNA detection in budding yeast with single fluorophores
Quantitative measurement of mRNA levels in single cells is necessary to understand phenotypic variability within an otherwise isogenic population of cells. Single-molecule mRNA Fluorescence In Situ Hybridization (FISH) has been established as the standard method for this purpose, but current protoco...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587780/ https://www.ncbi.nlm.nih.gov/pubmed/28666354 http://dx.doi.org/10.1093/nar/gkx568 |
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author | Wadsworth, Gable M. Parikh, Rasesh Y. Choy, John S. Kim, Harold D. |
author_facet | Wadsworth, Gable M. Parikh, Rasesh Y. Choy, John S. Kim, Harold D. |
author_sort | Wadsworth, Gable M. |
collection | PubMed |
description | Quantitative measurement of mRNA levels in single cells is necessary to understand phenotypic variability within an otherwise isogenic population of cells. Single-molecule mRNA Fluorescence In Situ Hybridization (FISH) has been established as the standard method for this purpose, but current protocols require a long region of mRNA to be targeted by multiple DNA probes. Here, we introduce a new single-probe FISH protocol termed sFISH for budding yeast, Saccharomyces cerevisiae using a single DNA probe labeled with a single fluorophore. In sFISH, we markedly improved probe specificity and signal-to-background ratio by using methanol fixation and inclined laser illumination. We show that sFISH reports mRNA changes that correspond to protein levels and gene copy number. Using this new FISH protocol, we can detect >50% of the total target mRNA. We also demonstrate the versatility of sFISH using FRET detection and mRNA isoform profiling as examples. Our FISH protocol with single-fluorophore sensitivity significantly reduces cost and time compared to the conventional FISH protocols and opens up new opportunities to investigate small changes in RNA at the single cell level. |
format | Online Article Text |
id | pubmed-5587780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55877802017-09-11 mRNA detection in budding yeast with single fluorophores Wadsworth, Gable M. Parikh, Rasesh Y. Choy, John S. Kim, Harold D. Nucleic Acids Res Methods Online Quantitative measurement of mRNA levels in single cells is necessary to understand phenotypic variability within an otherwise isogenic population of cells. Single-molecule mRNA Fluorescence In Situ Hybridization (FISH) has been established as the standard method for this purpose, but current protocols require a long region of mRNA to be targeted by multiple DNA probes. Here, we introduce a new single-probe FISH protocol termed sFISH for budding yeast, Saccharomyces cerevisiae using a single DNA probe labeled with a single fluorophore. In sFISH, we markedly improved probe specificity and signal-to-background ratio by using methanol fixation and inclined laser illumination. We show that sFISH reports mRNA changes that correspond to protein levels and gene copy number. Using this new FISH protocol, we can detect >50% of the total target mRNA. We also demonstrate the versatility of sFISH using FRET detection and mRNA isoform profiling as examples. Our FISH protocol with single-fluorophore sensitivity significantly reduces cost and time compared to the conventional FISH protocols and opens up new opportunities to investigate small changes in RNA at the single cell level. Oxford University Press 2017-09-06 2017-06-28 /pmc/articles/PMC5587780/ /pubmed/28666354 http://dx.doi.org/10.1093/nar/gkx568 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Methods Online Wadsworth, Gable M. Parikh, Rasesh Y. Choy, John S. Kim, Harold D. mRNA detection in budding yeast with single fluorophores |
title | mRNA detection in budding yeast with single fluorophores |
title_full | mRNA detection in budding yeast with single fluorophores |
title_fullStr | mRNA detection in budding yeast with single fluorophores |
title_full_unstemmed | mRNA detection in budding yeast with single fluorophores |
title_short | mRNA detection in budding yeast with single fluorophores |
title_sort | mrna detection in budding yeast with single fluorophores |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587780/ https://www.ncbi.nlm.nih.gov/pubmed/28666354 http://dx.doi.org/10.1093/nar/gkx568 |
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