Titlow Joshua S, Yang Lu, Parton Richard M, Palanca Ana, Davis Ilan
Department of Biochemistry, University of Oxford, South Parks Road, Oxford, OX1 3QU, UK.
Methods Mol Biol. 2018;1649:163-175. doi: 10.1007/978-1-4939-7213-5_10.
The lack of an effective, simple, and highly sensitive protocol for fluorescent in situ hybridization (FISH) at the Drosophila larval neuromuscular junction (NMJ) has hampered the study of mRNA biology. Here, we describe our modified single molecule FISH (smFISH) methods that work well in whole mount Drosophila NMJ preparations to quantify primary transcription and count individual cytoplasmic mRNA molecules in specimens while maintaining ultrastructural preservation. The smFISH method is suitable for high-throughput sample processing and 3D image acquisition using any conventional microscopy imaging modality and is compatible with the use of antibody colabeling and transgenic fluorescent protein tags in axons, glia, synapses, and muscle cells. These attributes make the method particularly amenable to super-resolution imaging. With 3D Structured Illumination Microscopy (3D-SIM), which increases spatial resolution by a factor of 2 in X, Y, and Z, we acquire super-resolution information about the distribution of single molecules of mRNA in relation to covisualized synaptic and cellular structures. Finally, we demonstrate the use of commercial and open source software for the quality control of single transcript expression analysis, 3D-SIM data acquisition and reconstruction as well as image archiving management and presentation. Our methods now allow the detailed mechanistic and functional analysis of sparse as well as abundant mRNAs at the NMJ in their appropriate cellular context.
在果蝇幼虫神经肌肉接头(NMJ)处缺乏一种有效、简单且高度灵敏的荧光原位杂交(FISH)方案,这阻碍了mRNA生物学的研究。在此,我们描述了我们改良的单分子FISH(smFISH)方法,该方法在果蝇NMJ整装标本中效果良好,可在保持超微结构保存的同时,对标本中的初级转录进行定量并计数单个细胞质mRNA分子。smFISH方法适用于使用任何传统显微镜成像方式进行高通量样品处理和3D图像采集,并且与轴突、神经胶质、突触和肌肉细胞中的抗体共标记以及转基因荧光蛋白标签的使用兼容。这些特性使得该方法特别适合超分辨率成像。通过在X、Y和Z方向上将空间分辨率提高2倍的3D结构光照明显微镜(3D-SIM),我们获得了关于mRNA单分子分布与共可视化的突触和细胞结构相关的超分辨率信息。最后,我们展示了使用商业和开源软件进行单转录本表达分析的质量控制、3D-SIM数据采集与重建以及图像存档管理和展示。我们的方法现在允许在适当的细胞背景下对NMJ处稀疏和丰富的mRNA进行详细的机制和功能分析。