单分子分辨率树突状rna的荧光原位成像

Q2 Neuroscience
Mona Batish, Sanjay Tyagi
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引用次数: 7

摘要

RNA定位是基因调控的重要步骤。固定细胞和活细胞中的RNA成像提供了细胞中RNA分布的背景信息。在这里,我们提供了执行单分子荧光原位杂交(smFISH)的详细方案。smFISH在固定神经元细胞中以单分子分辨率检测mRNA分子,每个mRNA使用约50个小的寡核苷酸探针。该技术已成功应用于了解RNA在各种生物系统中的定位和分布,范围从果蝇到哺乳动物神经系统。探针足够小,可以结合结构化RNA或RNA-蛋白复合物的一部分RNA,因此占总RNA的约85%;这使得灵敏度水平相当于定量实时PCR,但具有解剖分辨率。©2019 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fluorescence In Situ Imaging of Dendritic RNAs at Single-Molecule Resolution

RNA localization is an important step in gene regulation. Imaging RNAs in fixed and live cells provides contextual information about RNA distribution in the cells. Here, we provide detailed protocols for performing single-molecule fluorescence in situ hybridization (smFISH). smFISH detects mRNA molecules at single-molecule resolution in fixed neuronal cells using ∼50 small oligonucleotide probes for each mRNA. The technique has been successfully applied to understand RNA localization and distribution in various biological systems, ranging from Drosophila to the mammalian nervous system. The probes are small enough to bind to structured RNAs or RNAs that are part of RNA-protein complexes, thereby accounting for ∼85% of the total RNA; this enables a level of sensitivity equivalent to that of quantitative real-time PCR, but with anatomical resolution. © 2019 by John Wiley & Sons, Inc.

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来源期刊
Current Protocols in Neuroscience
Current Protocols in Neuroscience Neuroscience-Neuroscience (all)
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期刊介绍: Current Protocols in Neuroscience is a one-stop resource for finding and adapting the best models and methods for all types of neuroscience experiments. Updated every three months in all formats, CPNS is constantly evolving to keep pace with the very latest discoveries and developments. A year of these quarterly updates is included in the initial CPNS purchase price.
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