Lee Byung Hun, Bae Seong-Woo, Shim Jaeyoun Jay, Park Sung Young, Park Hye Yoon
Department of Physics and Astronomy, Seoul National University, Seoul 08826, Korea.
Center for RNA Research, Institute for Basic Science, Seoul 08826, Korea.
Mol Cells. 2016 Dec;39(12):841-846. doi: 10.14348/molcells.2016.0277. Epub 2016 Dec 29.
Local protein synthesis mediates precise spatio-temporal regulation of gene expression for neuronal functions such as long-term plasticity, axon guidance and regeneration. To reveal the underlying mechanisms of local translation, it is crucial to understand mRNA transport, localization and translation in live neurons. Among various techniques for mRNA analysis, fluorescence microscopy has been widely used as the most direct method to study localization of mRNA. Live-cell imaging of single RNA molecules is particularly advantageous to dissect the highly heterogeneous and dynamic nature of messenger ribonucleoprotein (mRNP) complexes in neurons. Here, we review recent advances in the study of mRNA localization and translation in live neurons using novel techniques for single-RNA imaging.
局部蛋白质合成介导了基因表达的精确时空调控,以实现诸如长期可塑性、轴突导向和再生等神经元功能。为了揭示局部翻译的潜在机制,了解活神经元中的mRNA运输、定位和翻译至关重要。在各种mRNA分析技术中,荧光显微镜已被广泛用作研究mRNA定位的最直接方法。对单个RNA分子进行活细胞成像,对于剖析神经元中信使核糖核蛋白(mRNP)复合物高度异质和动态的性质特别有利。在这里,我们综述了利用单RNA成像新技术在活神经元中mRNA定位和翻译研究方面的最新进展。