Allele-specific RNA imaging shows that allelic imbalances can arise in tissues through transcriptional bursting.
Orsolya SymmonsMarcello ChangIan A MellisJennifer M KalishJiwhan ParkKatalin SusztákMarisa S BartolomeiArjun RajPublished in: PLoS genetics (2019)
Extensive cell-to-cell variation exists even among putatively identical cells, and there is great interest in understanding how the properties of transcription relate to this heterogeneity. Differential expression from the two gene copies in diploid cells could potentially contribute, yet our ability to measure from which gene copy individual RNAs originated remains limited, particularly in the context of tissues. Here, we demonstrate quantitative, single molecule allele-specific RNA FISH adapted for use on tissue sections, allowing us to determine the chromosome of origin of individual RNA molecules in formaldehyde-fixed tissues. We used this method to visualize the allele-specific expression of Xist and multiple autosomal genes in mouse kidney. By combining these data with mathematical modeling, we evaluated models for allele-specific heterogeneity, in particular demonstrating that apparent expression from only one of the alleles in single cells can arise as a consequence of low-level mRNA abundance and transcriptional bursting.
Keyphrases
- induced apoptosis
- single cell
- single molecule
- gene expression
- cell cycle arrest
- poor prognosis
- genome wide
- transcription factor
- copy number
- high resolution
- cell therapy
- signaling pathway
- oxidative stress
- computed tomography
- genome wide identification
- magnetic resonance imaging
- stem cells
- mass spectrometry
- microbial community
- cell proliferation
- wastewater treatment
- fluorescent probe
- high speed
- diffusion weighted imaging