Multiplexed detection of RNA using MERFISH and branched DNA amplification

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作者
Chenglong Xia
Hazen P. Babcock
Jeffrey R. Moffitt
Xiaowei Zhuang
机构
[1] Howard Hughes Medical Institute,Center for Advanced Imaging
[2] Department of Chemistry and Chemical Biology,undefined
[3] and Department of Physics,undefined
[4] Harvard University,undefined
[5] Harvard University,undefined
[6] Program in Cellular and Molecular Medicine,undefined
[7] Boston Children’s Hospital; Department of Microbiology,undefined
[8] Harvard Medical School,undefined
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Multiplexed error-robust fluorescence in situ hybridization (MERFISH) allows simultaneous imaging of numerous RNA species in their native cellular environment and hence spatially resolved single-cell transcriptomic measurements. However, the relatively modest brightness of signals from single RNA molecules can become limiting in a number of applications, such as increasing the imaging throughput, imaging shorter RNAs, and imaging samples with high degrees of background, such as some tissue samples. Here, we report a branched DNA (bDNA) amplification approach for MERFISH measurements. This approach produces a drastic signal increase in RNA FISH samples without increasing the fluorescent spot size for individual RNAs or increasing the variation in brightness from spot to spot, properties that are important for MERFISH imaging. Using this amplification approach in combination with MERFISH, we demonstrated RNA imaging and profiling with a near 100% detection efficiency. We further demonstrated that signal amplification improves MERFISH performance when fewer FISH probes are used for each RNA species, which should allow shorter RNAs to be imaged. We anticipate that the combination of bDNA amplification with MERFISH should facilitate many other applications and extend the range of biological questions that can be addressed by this technique in both cell culture and tissues.
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