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smiFISH and FISH-quant – a flexible single RNA detection approach with super-resolution capability
Single molecule FISH (smFISH) allows studying transcription and RNA localization by imaging individual mRNAs in single cells. We present smiFISH (single molecule inexpensive FISH), an easy to use and flexible RNA visualization and quantification approach that uses unlabelled primary probes and a flu...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5159540/ https://www.ncbi.nlm.nih.gov/pubmed/27599845 http://dx.doi.org/10.1093/nar/gkw784 |
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author | Tsanov, Nikolay Samacoits, Aubin Chouaib, Racha Traboulsi, Abdel-Meneem Gostan, Thierry Weber, Christian Zimmer, Christophe Zibara, Kazem Walter, Thomas Peter, Marion Bertrand, Edouard Mueller, Florian |
author_facet | Tsanov, Nikolay Samacoits, Aubin Chouaib, Racha Traboulsi, Abdel-Meneem Gostan, Thierry Weber, Christian Zimmer, Christophe Zibara, Kazem Walter, Thomas Peter, Marion Bertrand, Edouard Mueller, Florian |
author_sort | Tsanov, Nikolay |
collection | PubMed |
description | Single molecule FISH (smFISH) allows studying transcription and RNA localization by imaging individual mRNAs in single cells. We present smiFISH (single molecule inexpensive FISH), an easy to use and flexible RNA visualization and quantification approach that uses unlabelled primary probes and a fluorescently labelled secondary detector oligonucleotide. The gene-specific probes are unlabelled and can therefore be synthesized at low cost, thus allowing to use more probes per mRNA resulting in a substantial increase in detection efficiency. smiFISH is also flexible since differently labelled secondary detector probes can be used with the same primary probes. We demonstrate that this flexibility allows multicolor labelling without the need to synthesize new probe sets. We further demonstrate that the use of a specific acrydite detector oligonucleotide allows smiFISH to be combined with expansion microscopy, enabling the resolution of transcripts in 3D below the diffraction limit on a standard microscope. Lastly, we provide improved, fully automated software tools from probe-design to quantitative analysis of smFISH images. In short, we provide a complete workflow to obtain automatically counts of individual RNA molecules in single cells. |
format | Online Article Text |
id | pubmed-5159540 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-51595402016-12-16 smiFISH and FISH-quant – a flexible single RNA detection approach with super-resolution capability Tsanov, Nikolay Samacoits, Aubin Chouaib, Racha Traboulsi, Abdel-Meneem Gostan, Thierry Weber, Christian Zimmer, Christophe Zibara, Kazem Walter, Thomas Peter, Marion Bertrand, Edouard Mueller, Florian Nucleic Acids Res Methods Online Single molecule FISH (smFISH) allows studying transcription and RNA localization by imaging individual mRNAs in single cells. We present smiFISH (single molecule inexpensive FISH), an easy to use and flexible RNA visualization and quantification approach that uses unlabelled primary probes and a fluorescently labelled secondary detector oligonucleotide. The gene-specific probes are unlabelled and can therefore be synthesized at low cost, thus allowing to use more probes per mRNA resulting in a substantial increase in detection efficiency. smiFISH is also flexible since differently labelled secondary detector probes can be used with the same primary probes. We demonstrate that this flexibility allows multicolor labelling without the need to synthesize new probe sets. We further demonstrate that the use of a specific acrydite detector oligonucleotide allows smiFISH to be combined with expansion microscopy, enabling the resolution of transcripts in 3D below the diffraction limit on a standard microscope. Lastly, we provide improved, fully automated software tools from probe-design to quantitative analysis of smFISH images. In short, we provide a complete workflow to obtain automatically counts of individual RNA molecules in single cells. Oxford University Press 2016-12-15 2016-09-05 /pmc/articles/PMC5159540/ /pubmed/27599845 http://dx.doi.org/10.1093/nar/gkw784 Text en © The Author(s) 2016. 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 Tsanov, Nikolay Samacoits, Aubin Chouaib, Racha Traboulsi, Abdel-Meneem Gostan, Thierry Weber, Christian Zimmer, Christophe Zibara, Kazem Walter, Thomas Peter, Marion Bertrand, Edouard Mueller, Florian smiFISH and FISH-quant – a flexible single RNA detection approach with super-resolution capability |
title | smiFISH and FISH-quant – a flexible single RNA detection approach with super-resolution capability |
title_full | smiFISH and FISH-quant – a flexible single RNA detection approach with super-resolution capability |
title_fullStr | smiFISH and FISH-quant – a flexible single RNA detection approach with super-resolution capability |
title_full_unstemmed | smiFISH and FISH-quant – a flexible single RNA detection approach with super-resolution capability |
title_short | smiFISH and FISH-quant – a flexible single RNA detection approach with super-resolution capability |
title_sort | smifish and fish-quant – a flexible single rna detection approach with super-resolution capability |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5159540/ https://www.ncbi.nlm.nih.gov/pubmed/27599845 http://dx.doi.org/10.1093/nar/gkw784 |
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