Single Molecule Analysis Group, Department of Chemistry, University of Michigan, Ann Arbor, Michigan.
Biophysics Graduate Program, University of Michigan, Ann Arbor, Michigan.
Wiley Interdiscip Rev RNA. 2020 Jul;11(4):e1587. doi: 10.1002/wrna.1587. Epub 2020 Jan 28.
Messenger RNAs (mRNAs) convey genetic information from the DNA genome to proteins and thus lie at the heart of gene expression and regulation of all cellular activities. Live cell single molecule tracking tools enable the investigation of mRNA trafficking, translation and degradation within the complex environment of the cell and in real time. Over the last 5 years, nearly all tools within the mRNA tracking toolbox have been improved to achieve high-quality multi-color tracking in live cells. For example, the bacteriophage-derived MS2-MCP system has been improved to facilitate cloning and achieve better signal-to-noise ratio, while the newer PP7-PCP system now allows for orthogonal tracking of a second mRNA or mRNA region. The coming of age of epitope-tagging technologies, such as the SunTag, MoonTag and Frankenbody, enables monitoring the translation of single mRNA molecules. Furthermore, the portfolio of fluorogenic RNA aptamers has been expanded to improve cellular stability and achieve a higher fluorescence "turn-on" signal upon fluorogen binding. Finally, microinjection-based tools have been shown to be able to track multiple RNAs with only small fluorescent appendages and to track mRNAs together with their interacting partners. We systematically review and compare the advantages, disadvantages and demonstrated applications in discovering new RNA biology of this refined, expanding toolbox. Finally, we discuss developments expected in the near future based on the limitations of the current methods. This article is categorized under: RNA Export and Localization > RNA Localization RNA Structure and Dynamics > RNA Structure, Dynamics, and Chemistry RNA Interactions with Proteins and Other Molecules > RNA-Protein Complexes.
信使 RNA(mRNA)将遗传信息从 DNA 基因组传递到蛋白质,因此处于基因表达和调控所有细胞活动的核心。活细胞单分子跟踪工具能够在细胞的复杂环境中实时研究 mRNA 的运输、翻译和降解。在过去的 5 年中,mRNA 跟踪工具箱中的几乎所有工具都得到了改进,以实现高质量的多色活细胞跟踪。例如,噬菌体衍生的 MS2-MCP 系统已得到改进,以方便克隆并获得更好的信噪比,而更新的 PP7-PCP 系统现在允许对第二个 mRNA 或 mRNA 区域进行正交跟踪。表位标记技术(如 SunTag、MoonTag 和 Frankenbody)的出现,使人们能够监测单个 mRNA 分子的翻译。此外,荧光 RNA 适体的组合已经扩大,以提高细胞稳定性,并在荧光团结合时实现更高的荧光“开启”信号。最后,基于微注射的工具已被证明能够用只有小荧光附属物跟踪多个 RNA,并与它们的相互作用伙伴一起跟踪 mRNAs。我们系统地回顾和比较了这个经过改进和扩展的工具箱的优点、缺点和在发现新的 RNA 生物学方面的应用。最后,我们根据当前方法的局限性讨论了未来的发展。本文归类于:RNA 输出和定位 > RNA 定位 RNA 结构和动态 > RNA 结构、动态和化学 RNA 与蛋白质和其他分子的相互作用 > RNA-蛋白质复合物。