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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
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.
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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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