Turbo FISH: A Method for Rapid Single Molecule RNA FISH

被引:73
作者
Shaffer, Sydney M. [1 ]
Wu, Min-Tzu [1 ]
Levesque, Marshall J. [1 ]
Raj, Arjun [1 ]
机构
[1] Univ Penn, Dept Bioengn, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
STOCHASTIC GENE-EXPRESSION; TRANSCRIPTS IN-SITU; LABELED PROBES; CELL; LOCALIZATION; QPCR;
D O I
10.1371/journal.pone.0075120
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Advances in RNA fluorescence in situ hybridization (RNA FISH) have allowed practitioners to detect individual RNA molecules in single cells via fluorescence microscopy, enabling highly accurate and sensitive quantification of gene expression. However, current methods typically employ hybridization times on the order of 2-16 hours, limiting its potential in applications like rapid diagnostics. We present here a set of conditions for RNA FISH (dubbed Turbo RNA FISH) that allow us to make accurate measurements with no more than 5 minutes of hybridization time and 3 minutes of washing, and show that hybridization times can go as low as 30 seconds while still producing quantifiable images. We further show that rapid hybridization is compatible with our recently developed iceFISH and SNP FISH variants of RNA FISH that enable chromosome and single base discrimination, respectively. Our method is simple and cost effective, and has the potential to dramatically increase the throughput and realm of applicability of RNA FISH.
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页数:9
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