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smiFISH and FISH-quant – a flexible single RNA detection approach with super-resolution capability
Author(s) -
Nikolay Tsanov,
Aubin Samacoïts,
Racha Chouaib,
Abdel-Meneem Traboulsi,
Thierry Gostan,
Christian Weber,
Christophe Zimmer,
Kazem Zibara,
Thomas Walter,
Marion Peter,
Édouard Bertrand,
Florian Mueller
Publication year - 2016
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gkw784
Subject(s) - biology , oligonucleotide , rna , computational biology , detector , microscopy , biophysics , microbiology and biotechnology , gene , genetics , physics , optics
International audienceSingle 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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