放大器
计算生物学
滚动圆复制
核糖核酸
荧光显微镜
DNA
生物
基因
遗传学
荧光
聚合酶链反应
DNA聚合酶
物理
光学
作者
Ruijie Deng,Kaixiang Zhang,Lida Wang,Xiaojun Ren,Yupeng Sun,Jinghong Li
出处
期刊:Chem
[Elsevier BV]
日期:2018-04-12
卷期号:4 (6): 1373-1386
被引量:159
标识
DOI:10.1016/j.chempr.2018.03.003
摘要
The expression and spatial profile of multiple RNA species at high precision in single cells is key information for understanding cellular behaviors and functions. Fluorescence microscopy is a powerful tool for imaging RNAs, but its multiplexing ability is limited by the number of spectrally distinct fluorophores. Here, we present a DNA-sequence-encoded fluorescence barcoding method, termed sequence-encoded amplicon (SeqEA), enabling highly multiplexed imaging of RNAs in single cells with single-molecule and single-nucleotide resolution. SeqEA exploits a thermodynamically tuning DNA hybridization approach for precisely encoding rolling circle amplicons with discrete fluorescence intensities as fluorescence barcodes, allowing for multiplexed tagging single-molecule RNAs. As a proof of principle, we have demonstrated its ability for simultaneously visualizing nine mRNA species and evaluated the coordination and spatial pattern of breast-cancer-associated oncogene expression. SeqEA provides a single-cell analysis platform for investigating the gene expression network and molecular mechanism of disease development.
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