Cell Biology of Genomes, Center for Cancer Research (CCR), National Cancer Institute, NIH, Bethesda, MD, USA.
High-Throughput Imaging Facility (HiTIF), Center for Cancer Research (CCR), National Cancer Institute, NIH, Bethesda, MD, USA.
Methods Mol Biol. 2024;2784:133-146. doi: 10.1007/978-1-0716-3766-1_9.
RNA-fluorescence in situ hybridization (RNA-FISH) is an essential and widely used tool for visualizing RNA molecules in intact cells. Recent advances have increased RNA-FISH sensitivity, signal detection efficiency, and throughput. However, detection of endogenous mRNA splice variants has been challenging due to the limits of visualization of RNA-FISH fluorescence signals and due to the limited number of RNA-FISH probes per target. HiFENS (high-throughput FISH detection of endogenous pre-mRNA splicing isoforms) is a method that enables visualization and relative quantification of mRNA splice variants at single-cell resolution in an automated high-throughput manner. HiFENS incorporates HCR (hybridization chain reaction) signal amplification strategies to enhance the fluorescence signal generated by low abundance transcripts or a small number of FISH probes targeting short stretches of RNA, such as single exons. The technique offers a significant advance in high-throughput FISH-based RNA detection and provides a powerful tool that can be used as a readout in functional genomics screens to discover and dissect cellular pathways regulating gene expression and alternative pre-mRNA splicing events.
RNA 荧光原位杂交(RNA-FISH)是一种用于在完整细胞中可视化 RNA 分子的重要且广泛使用的工具。最近的进展提高了 RNA-FISH 的灵敏度、信号检测效率和通量。然而,由于 RNA-FISH 荧光信号的可视化限制以及每个靶标可用的 RNA-FISH 探针数量有限,内源性 mRNA 剪接变体的检测一直具有挑战性。HiFENS(内源性前体 mRNA 剪接异构体的高通量 FISH 检测)是一种能够以自动化高通量方式在单细胞分辨率下可视化和相对定量 mRNA 剪接变体的方法。HiFENS 采用 HCR(杂交链反应)信号扩增策略来增强低丰度转录本或针对短 RNA 区域(如单个外显子)的少量 FISH 探针产生的荧光信号。该技术在基于高通量 FISH 的 RNA 检测方面取得了重大进展,提供了一种强大的工具,可用作功能基因组学筛选的读数,以发现和剖析调节基因表达和替代前体 mRNA 剪接事件的细胞途径。