用于成像tRNA衍生RNA生物发生的自猝灭tRNA报告器。

4区 生物学 Q3 Biochemistry, Genetics and Molecular Biology
Methods in enzymology Pub Date : 2025-01-01 Epub Date: 2024-12-03 DOI:10.1016/bs.mie.2024.11.025
Guoping Li, Saumya Das
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引用次数: 0

摘要

trna衍生的小rna (tDRs)是一类新兴的小非编码rna,在各种细胞过程中起着至关重要的作用。然而,由于缺乏成像tdr的工具和试剂,缺乏关于其亚细胞定位的数据。由于tDR与其亲本tRNA之间的序列相似,成像tDR仍然具有挑战性。在这里,我们描述了一种创新的工具,用于研究tDR的形成和定位在各种生物过程中使用自猝灭tDR生物发生报告。该方法利用全长tRNA分子在5'-和3'-端结合荧光基团和猝灭基团。在其完整状态下,荧光被淬灭。在特定的核糖核酸酶切割和链分离后,荧光变得可检测,允许实时成像tDR生物发生。本协议详细介绍了该报告的设计、合成和应用,包括转染程序和成像技术。该方法为研究活细胞中的tDR动力学提供了一种强有力的方法,可以深入了解它们在细胞过程和应激反应中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Self-quenched tRNA reporters for imaging tRNA-derived RNA biogenesis.

tRNA-derived small RNAs (tDRs) are an emerging class of small non-coding RNAs that play crucial roles in various cellular processes. However, there is a paucity of data on their sub-cellular localization due to a lack of tools and reagents to image tDRs. Imaging tDRs remains challenging due to the similar sequences between tDR and its parent tRNA. Here, we describe an innovative tool for studying the formation and localization of tDRs in various biological processes using a self-quenched tDR biogenesis reporter. This method utilizes a full-length tRNA molecule conjugated with both fluorescence and quencher groups at 5'- and 3'- ends. In its intact state, the fluorescence is quenched. Upon cleavage by specific ribonucleases and strand separation, the fluorescence becomes detectable, allowing real-time imaging of tDR biogenesis. This protocol details the design, synthesis, and application of this reporter, including transfection procedures and imaging techniques. The method offers a powerful approach for investigating tDR dynamics in living cells, providing insights into their roles in cellular processes and stress responses.

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来源期刊
Methods in enzymology
Methods in enzymology 生物-生化研究方法
CiteScore
2.90
自引率
0.00%
发文量
308
审稿时长
3-6 weeks
期刊介绍: The critically acclaimed laboratory standard for almost 50 years, Methods in Enzymology is one of the most highly respected publications in the field of biochemistry. Each volume is eagerly awaited, frequently consulted, and praised by researchers and reviewers alike. Now with over 500 volumes the series contains much material still relevant today and is truly an essential publication for researchers in all fields of life sciences, including microbiology, biochemistry, cancer research and genetics-just to name a few. Five of the 2013 Nobel Laureates have edited or contributed to volumes of MIE.
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