Chen Jingxun, McSwiggen David, Ünal Elçin
Department of Molecular and Cell Biology, Barker Hall, University of California, Berkeley.
Department of Molecular and Cell Biology, Li Ka Shing Center, University of California, Berkeley.
J Vis Exp. 2018 May 25(135):57774. doi: 10.3791/57774.
Single molecule fluorescence in situ hybridization (smFISH) is a powerful technique to study gene expression in single cells due to its ability to detect and count individual RNA molecules. Complementary to deep sequencing-based methods, smFISH provides information about the cell-to-cell variation in transcript abundance and the subcellular localization of a given RNA. Recently, we have used smFISH to study the expression of the gene NDC80 during meiosis in budding yeast, in which two transcript isoforms exist and the short transcript isoform has its entire sequence shared with the long isoform. To confidently identify each transcript isoform, we optimized known smFISH protocols and obtained high consistency and quality of smFISH data for the samples acquired during budding yeast meiosis. Here, we describe this optimized protocol, the criteria that we use to determine whether high quality of smFISH data is obtained, and some tips for implementing this protocol in other yeast strains and growth conditions.
单分子荧光原位杂交(smFISH)是一种强大的技术,可用于研究单细胞中的基因表达,因为它能够检测和计数单个RNA分子。与基于深度测序的方法互补,smFISH提供了有关转录本丰度的细胞间变异以及给定RNA的亚细胞定位的信息。最近,我们使用smFISH研究了芽殖酵母减数分裂过程中NDC80基因的表达,其中存在两种转录本异构体,短转录本异构体的整个序列与长异构体共享。为了可靠地识别每种转录本异构体,我们优化了已知的smFISH方案,并为芽殖酵母减数分裂期间获取的样本获得了高度一致和高质量的smFISH数据。在这里,我们描述了这个优化的方案、我们用于确定是否获得高质量smFISH数据的标准,以及在其他酵母菌株和生长条件下实施该方案的一些提示。