Single molecule fluorescence in situ hybridisation for quantitating post-transcriptional regulation in Drosophila brains

- Simple and rapid smFISH protocol suitable for medium throughput.
- Sensitive mRNA detection deep in whole-mount larval and adult Drosophila brains.
- Multiplexed detection of RNA in combination with antibody staining.
- Quantitation of primary transcription and post-transcriptional mRNA levels.
- Reliable cell type markers in a whole-mount brain complementary to antibody markers.

RNA in situ hybridization is a powerful method to investigate post-transcriptional regulation, but analysis of intracellular mRNA distributions in thick, complex tissues like the brain poses significant challenges. Here, we describe the application of single-molecule fluorescent in situ hybridization (smFISH) to quantitate primary nascent transcription and post-transcriptional regulation in whole-mount Drosophila larval and adult brains. Combining immunofluorescence and smFISH probes for different regions of a single gene, i.e., exons, 3′UTR, and introns, we show examples of a gene that is regulated post-transcriptionally and one that is regulated at the level of transcription. Our simple and rapid protocol can be used to co-visualise a variety of different transcripts and proteins in neuronal stem cells as well as deep brain structures such as mushroom body neuropils, using conventional confocal microscopy. Finally, we introduce the use of smFISH as a sensitive alternative to immunofluorescence for labelling specific neural stem cell populations in the brain.