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RNAscope? and BaseScope?: In-situ RNA analysis for formalin-fixed paraffin-embedded tissues and beyond

机译:rnascope?和底座?:福尔马林固定石蜡包埋组织及超越的原位RNA分析

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In-situ hybridization (ISH) analysis is a highly desirable, versatile approach for assessing biomarker expression status in a spatial context. Most researchers rely on immunostaining (protein targets) or qPCR (mRNA). However, not all proteins can be immunolabeled due to a lack of well-validated antibodies. The qPCR approach, although highly specific, cannot provide spatial information. RNAscope? employs a unique double Z probe that has to bind to the target RNA in tandem in order to be recognized by the preamplifiers and amplifiers. A fluorescent/chromogenic labeled probe then binds to the multiple binding sites of the amplifiers, which improves detection of low expressing RNA and reduces non-specific binding. RNAscope? replaces cumbersome radioactive and chromogenic ISH with more hassle-free chromogen and fluorescence-labelled probes. At the NYULMC Experimental Pathology Core we have integrated RNAscope? with Polaris multispectral imaging and quantitative analysis using different software platforms. About 21 laboratories have used this workflow to address their specific questions. We have also established and validated the newer BaseScope? assay. In contrast to RNAscope?, which targets lncRNA and mRNA sequences greater than 300nt, BaseScope? enables detection of short RNA target sequences between 50-300nt. It can be used to detect exon junctions/splice variants, circular RNA, pre-miRNA, and point mutations. We adapted BaseScope? to co-detect circular RNA and its linear counterpart in a differentiating cell population, which could not be established on glass chamber slides and had to be stained on a plastic petri dish. In conclusion, RNAscope? and BaseScope? RNA-ISH are powerful alternative strategies for assessing the spatial distribution of critical biomarkers within intact tissues and cells. This approach coupled with sophisticated imaging modalities and downstream analysis support provides new collaborative opportunities for Core aboratories.
机译:原位杂交(ISH)分析是一种非常理想的通用方法,用于评估空间背景下的生物标志物表达状态。大多数研究人员依赖于免疫染色(蛋白质靶标)或QPCR(mRNA)。然而,由于缺乏良好验证的抗体,并非所有蛋白质都可以免疫标记。 QPCR方法虽然非常具体,但不能提供空间信息。 rnascope?采用独特的双Z探针,该探针必须与串联的目标RNA结合,以便被前置放大器和放大器识别。然后将荧光/色发色标记探针结合到放大器的多个结合位点,这改善了低表达RNA的检测并减少了非特异性结合。 rnascope?用更多的无忧曲的色原和荧光标记的探针取代麻麻痹的放射性和色发球菌。在Nyulmc实验病理核心我们有集成的rnascope?使用不同的软件平台进行Polaris MultiSpectral成像和定量分析。大约21个实验室使用了这个工作流程来解决他们的具体问题。我们还建立并验证了较新的基础群岛?测定。与rnascope相反,靶向lncrna和mRNA序列大于300nt,basecrope?能够检测50-300NT之间的短RNA靶序列。它可用于检测外显子性连接/剪接变体,圆形RNA,预miRNA和点突变。我们改编为底座?在玻璃室的载玻片上共同检测圆形RNA及其线性对应物,不能在玻璃室载玻片上建立,并且必须在塑料培养皿上染色。总之,疯狂?和底座? RNA-ISH是用于评估完整组织和细胞内关键生物标志物的空间分布的强大替代策略。这种方法与复杂的成像方式和下游分析支持相结合,为核心存档提供了新的协作机会。

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