Institut de Génétique Moléculaire de Montpellier, Université de Montpellier, CNRS, Montpellier, France; Equipe labélisée Ligue Nationale Contre le Cancer, Montpellier, France.
Institut de Génétique Moléculaire de Montpellier, Université de Montpellier, CNRS, Montpellier, France.
Mol Cell. 2018 Aug 2;71(3):468-480. doi: 10.1016/j.molcel.2018.07.022.
The spatiotemporal regulation of gene expression is key to many biological processes. Recent imaging approaches opened exciting perspectives for understanding the intricate mechanisms regulating RNA metabolism, from synthesis to decay. Imaging techniques allow their observation at high spatial and temporal resolution, while keeping cellular morphology and micro-environment intact. Here, we focus on approaches for imaging single RNA molecules in cells, tissues, and embryos. In fixed cells, the rapid development of smFISH multiplexing opens the way to large-scale single-molecule studies, while in live cells, gene expression can be observed in real time in its native context. We highlight the strengths and limitations of these methods, as well as future challenges. We present how they advanced our understanding of gene expression heterogeneity and bursting, as well as the spatiotemporal aspects of splicing, translation, and RNA decay. These insights yield a dynamic and stochastic view of gene expression in single cells.
基因表达的时空调控是许多生物过程的关键。最近的成像方法为理解从合成到降解的 RNA 代谢调控的复杂机制开辟了令人兴奋的前景。成像技术允许在保持细胞形态和微环境完整的情况下,以高时空分辨率对其进行观察。在这里,我们重点介绍在细胞、组织和胚胎中对单个 RNA 分子进行成像的方法。在固定细胞中,smFISH 多重化的快速发展为大规模的单分子研究开辟了道路,而在活细胞中,可以在其天然环境中实时观察基因表达。我们强调了这些方法的优缺点以及未来的挑战。我们介绍了它们如何提高我们对基因表达异质性和爆发的理解,以及剪接、翻译和 RNA 降解的时空方面。这些见解为单细胞中的基因表达提供了一个动态和随机的视角。