| Autor: |
Chen J; Department of Molecular and Cell Biology, Barker Hall, University of California, Berkeley., McSwiggen D; Department of Molecular and Cell Biology, Li Ka Shing Center, University of California, Berkeley., Ünal E; Department of Molecular and Cell Biology, Barker Hall, University of California, Berkeley; elcin@berkeley.edu. |
| Jazyk: |
angličtina |
| Zdroj: |
Journal of visualized experiments : JoVE [J Vis Exp] 2018 May 25 (135). Date of Electronic Publication: 2018 May 25. |
| DOI: |
10.3791/57774 |
| Abstrakt: |
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. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
|
