Cargando…
Rapid quantification of miRNAs using dynamic FRET-FISH
MicroRNAs (miRNAs) are short regulatory RNAs that control gene expression at the post-transcriptional level. Various miRNAs playing important roles in cancer development are emerging as promising diagnostic biomarkers for early cancer detection. Accurate miRNA detection, however, remains challenging...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546913/ https://www.ncbi.nlm.nih.gov/pubmed/36207395 http://dx.doi.org/10.1038/s42003-022-04036-x |
_version_ | 1784805151603687424 |
---|---|
author | Kim, Juyoung Kang, Chanshin Shin, Soochul Hohng, Sungchul |
author_facet | Kim, Juyoung Kang, Chanshin Shin, Soochul Hohng, Sungchul |
author_sort | Kim, Juyoung |
collection | PubMed |
description | MicroRNAs (miRNAs) are short regulatory RNAs that control gene expression at the post-transcriptional level. Various miRNAs playing important roles in cancer development are emerging as promising diagnostic biomarkers for early cancer detection. Accurate miRNA detection, however, remains challenging because they are small and highly homologous. Recently developed miRNA detection techniques based on single-molecule imaging enabled highly specific miRNA quantification without amplification, but the time required for these techniques to detect a single miRNA was larger than 10 minutes, making rapid profiling of numerous miRNAs impractical. Here we report a rapid miRNA detection technique, dynamic FRET-FISH, in which single-molecule imaging at high probe concentrations and thus high-speed miRNA detection is possible. Dynamic FRET-FISH can detect miRNAs in 10 s at 1.2 μM probe concentration while maintaining the high-specificity of single-nucleotide discrimination. We expect dynamic FRET-FISH will be utilized for early detection of cancers by profiling hundreds of cancer biomarkers in an hour. |
format | Online Article Text |
id | pubmed-9546913 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95469132022-10-09 Rapid quantification of miRNAs using dynamic FRET-FISH Kim, Juyoung Kang, Chanshin Shin, Soochul Hohng, Sungchul Commun Biol Article MicroRNAs (miRNAs) are short regulatory RNAs that control gene expression at the post-transcriptional level. Various miRNAs playing important roles in cancer development are emerging as promising diagnostic biomarkers for early cancer detection. Accurate miRNA detection, however, remains challenging because they are small and highly homologous. Recently developed miRNA detection techniques based on single-molecule imaging enabled highly specific miRNA quantification without amplification, but the time required for these techniques to detect a single miRNA was larger than 10 minutes, making rapid profiling of numerous miRNAs impractical. Here we report a rapid miRNA detection technique, dynamic FRET-FISH, in which single-molecule imaging at high probe concentrations and thus high-speed miRNA detection is possible. Dynamic FRET-FISH can detect miRNAs in 10 s at 1.2 μM probe concentration while maintaining the high-specificity of single-nucleotide discrimination. We expect dynamic FRET-FISH will be utilized for early detection of cancers by profiling hundreds of cancer biomarkers in an hour. Nature Publishing Group UK 2022-10-07 /pmc/articles/PMC9546913/ /pubmed/36207395 http://dx.doi.org/10.1038/s42003-022-04036-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kim, Juyoung Kang, Chanshin Shin, Soochul Hohng, Sungchul Rapid quantification of miRNAs using dynamic FRET-FISH |
title | Rapid quantification of miRNAs using dynamic FRET-FISH |
title_full | Rapid quantification of miRNAs using dynamic FRET-FISH |
title_fullStr | Rapid quantification of miRNAs using dynamic FRET-FISH |
title_full_unstemmed | Rapid quantification of miRNAs using dynamic FRET-FISH |
title_short | Rapid quantification of miRNAs using dynamic FRET-FISH |
title_sort | rapid quantification of mirnas using dynamic fret-fish |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546913/ https://www.ncbi.nlm.nih.gov/pubmed/36207395 http://dx.doi.org/10.1038/s42003-022-04036-x |
work_keys_str_mv | AT kimjuyoung rapidquantificationofmirnasusingdynamicfretfish AT kangchanshin rapidquantificationofmirnasusingdynamicfretfish AT shinsoochul rapidquantificationofmirnasusingdynamicfretfish AT hohngsungchul rapidquantificationofmirnasusingdynamicfretfish |