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Analysis of RNA base modification and structural rearrangement by single-molecule real-time detection of reverse transcription
BACKGROUND: Zero-mode waveguides (ZMWs) are photonic nanostructures that create highly confined optical observation volumes, thereby allowing single-molecule-resolved biophysical studies at relatively high concentrations of fluorescent molecules. This principle has been successfully applied in singl...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3623877/ https://www.ncbi.nlm.nih.gov/pubmed/23552456 http://dx.doi.org/10.1186/1477-3155-11-8 |
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author | Vilfan, Igor D Tsai, Yu-Chih Clark, Tyson A Wegener, Jeffrey Dai, Qing Yi, Chengqi Pan, Tao Turner, Stephen W Korlach, Jonas |
author_facet | Vilfan, Igor D Tsai, Yu-Chih Clark, Tyson A Wegener, Jeffrey Dai, Qing Yi, Chengqi Pan, Tao Turner, Stephen W Korlach, Jonas |
author_sort | Vilfan, Igor D |
collection | PubMed |
description | BACKGROUND: Zero-mode waveguides (ZMWs) are photonic nanostructures that create highly confined optical observation volumes, thereby allowing single-molecule-resolved biophysical studies at relatively high concentrations of fluorescent molecules. This principle has been successfully applied in single-molecule, real-time (SMRT®) DNA sequencing for the detection of DNA sequences and DNA base modifications. In contrast, RNA sequencing methods cannot provide sequence and RNA base modifications concurrently as they rely on complementary DNA (cDNA) synthesis by reverse transcription followed by sequencing of cDNA. Thus, information on RNA modifications is lost during the process of cDNA synthesis. RESULTS: Here we describe an application of SMRT technology to follow the activity of reverse transcriptase enzymes synthesizing cDNA on thousands of single RNA templates simultaneously in real time with single nucleotide turnover resolution using arrays of ZMWs. This method thereby obtains information from the RNA template directly. The analysis of the kinetics of the reverse transcriptase can be used to identify RNA base modifications, shown by example for N6-methyladenine (m(6)A) in oligonucleotides and in a specific mRNA extracted from total cellular mRNA. Furthermore, the real-time reverse transcriptase dynamics informs about RNA secondary structure and its rearrangements, as demonstrated on a ribosomal RNA and an mRNA template. CONCLUSIONS: Our results highlight the feasibility of studying RNA modifications and RNA structural rearrangements in ZMWs in real time. In addition, they suggest that technology can be developed for direct RNA sequencing provided that the reverse transcriptase is optimized to resolve homonucleotide stretches in RNA. |
format | Online Article Text |
id | pubmed-3623877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36238772013-04-15 Analysis of RNA base modification and structural rearrangement by single-molecule real-time detection of reverse transcription Vilfan, Igor D Tsai, Yu-Chih Clark, Tyson A Wegener, Jeffrey Dai, Qing Yi, Chengqi Pan, Tao Turner, Stephen W Korlach, Jonas J Nanobiotechnology Methodology BACKGROUND: Zero-mode waveguides (ZMWs) are photonic nanostructures that create highly confined optical observation volumes, thereby allowing single-molecule-resolved biophysical studies at relatively high concentrations of fluorescent molecules. This principle has been successfully applied in single-molecule, real-time (SMRT®) DNA sequencing for the detection of DNA sequences and DNA base modifications. In contrast, RNA sequencing methods cannot provide sequence and RNA base modifications concurrently as they rely on complementary DNA (cDNA) synthesis by reverse transcription followed by sequencing of cDNA. Thus, information on RNA modifications is lost during the process of cDNA synthesis. RESULTS: Here we describe an application of SMRT technology to follow the activity of reverse transcriptase enzymes synthesizing cDNA on thousands of single RNA templates simultaneously in real time with single nucleotide turnover resolution using arrays of ZMWs. This method thereby obtains information from the RNA template directly. The analysis of the kinetics of the reverse transcriptase can be used to identify RNA base modifications, shown by example for N6-methyladenine (m(6)A) in oligonucleotides and in a specific mRNA extracted from total cellular mRNA. Furthermore, the real-time reverse transcriptase dynamics informs about RNA secondary structure and its rearrangements, as demonstrated on a ribosomal RNA and an mRNA template. CONCLUSIONS: Our results highlight the feasibility of studying RNA modifications and RNA structural rearrangements in ZMWs in real time. In addition, they suggest that technology can be developed for direct RNA sequencing provided that the reverse transcriptase is optimized to resolve homonucleotide stretches in RNA. BioMed Central 2013-04-03 /pmc/articles/PMC3623877/ /pubmed/23552456 http://dx.doi.org/10.1186/1477-3155-11-8 Text en Copyright © 2013 Vilfan et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Vilfan, Igor D Tsai, Yu-Chih Clark, Tyson A Wegener, Jeffrey Dai, Qing Yi, Chengqi Pan, Tao Turner, Stephen W Korlach, Jonas Analysis of RNA base modification and structural rearrangement by single-molecule real-time detection of reverse transcription |
title | Analysis of RNA base modification and structural rearrangement by single-molecule real-time detection of reverse transcription |
title_full | Analysis of RNA base modification and structural rearrangement by single-molecule real-time detection of reverse transcription |
title_fullStr | Analysis of RNA base modification and structural rearrangement by single-molecule real-time detection of reverse transcription |
title_full_unstemmed | Analysis of RNA base modification and structural rearrangement by single-molecule real-time detection of reverse transcription |
title_short | Analysis of RNA base modification and structural rearrangement by single-molecule real-time detection of reverse transcription |
title_sort | analysis of rna base modification and structural rearrangement by single-molecule real-time detection of reverse transcription |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3623877/ https://www.ncbi.nlm.nih.gov/pubmed/23552456 http://dx.doi.org/10.1186/1477-3155-11-8 |
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