Reference genes for quantitative Arabidopsis single molecule RNA fluorescence in situ hybridization.
Susan DuncanHans E JohanssonYiliang DingPublished in: Journal of experimental botany (2022)
Subcellular mRNA quantities and spatial distributions are fundamental for driving gene regulatory programs. Single molecule RNA FISH (smFISH) uses fluorescent probes to label individual mRNA molecules, thereby facilitating both localisation and quantitative studies. Validated reference mRNAs function as positive controls and are required for calibration. Here we present selection criteria for the first set of Arabidopsis smFISH reference genes. Following sequence and transcript data assessments, four mRNA probe sets were selected for imaging. Transcript counts per cell, correlations with cell size and corrected fluorescence intensities were all calculated for comparison. In addition to validating reference probe sets, we present sample preparation steps that can retain GFP fluorescence, thereby providing a method for simultaneous RNA and protein detection. In summary, our reference gene analyses, modified protocol and simplified quantification method together provide a firm foundation for future quantitative single molecule RNA studies in Arabidopsis root apical meristem cells.
Keyphrases
- single molecule
- living cells
- high resolution
- transcription factor
- atomic force microscopy
- single cell
- genome wide identification
- genome wide
- binding protein
- cell therapy
- rna seq
- randomized controlled trial
- induced apoptosis
- nucleic acid
- gene expression
- stem cells
- machine learning
- amino acid
- mass spectrometry
- cell proliferation
- cell cycle arrest
- artificial intelligence
- endoplasmic reticulum stress
- current status
- label free
- mesenchymal stem cells
- tandem mass spectrometry