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Multiplexed detection of RNA using MERFISH and branched DNA amplification
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 mo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531529/ https://www.ncbi.nlm.nih.gov/pubmed/31118500 http://dx.doi.org/10.1038/s41598-019-43943-8 |
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author | Xia, Chenglong Babcock, Hazen P. Moffitt, Jeffrey R. Zhuang, Xiaowei |
author_facet | Xia, Chenglong Babcock, Hazen P. Moffitt, Jeffrey R. Zhuang, Xiaowei |
author_sort | Xia, Chenglong |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6531529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65315292019-06-04 Multiplexed detection of RNA using MERFISH and branched DNA amplification Xia, Chenglong Babcock, Hazen P. Moffitt, Jeffrey R. Zhuang, Xiaowei Sci Rep Article 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. Nature Publishing Group UK 2019-05-22 /pmc/articles/PMC6531529/ /pubmed/31118500 http://dx.doi.org/10.1038/s41598-019-43943-8 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Xia, Chenglong Babcock, Hazen P. Moffitt, Jeffrey R. Zhuang, Xiaowei Multiplexed detection of RNA using MERFISH and branched DNA amplification |
title | Multiplexed detection of RNA using MERFISH and branched DNA amplification |
title_full | Multiplexed detection of RNA using MERFISH and branched DNA amplification |
title_fullStr | Multiplexed detection of RNA using MERFISH and branched DNA amplification |
title_full_unstemmed | Multiplexed detection of RNA using MERFISH and branched DNA amplification |
title_short | Multiplexed detection of RNA using MERFISH and branched DNA amplification |
title_sort | multiplexed detection of rna using merfish and branched dna amplification |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531529/ https://www.ncbi.nlm.nih.gov/pubmed/31118500 http://dx.doi.org/10.1038/s41598-019-43943-8 |
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