Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Vilfan, Igor D, Tsai, Yu-Chih, Clark, Tyson A, Wegener, Jeffrey, Dai, Qing, Yi, Chengqi, Pan, Tao, Turner, Stephen W, Korlach, Jonas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
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
_version_ 1782265986317025280
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
work_keys_str_mv AT vilfanigord analysisofrnabasemodificationandstructuralrearrangementbysinglemoleculerealtimedetectionofreversetranscription
AT tsaiyuchih analysisofrnabasemodificationandstructuralrearrangementbysinglemoleculerealtimedetectionofreversetranscription
AT clarktysona analysisofrnabasemodificationandstructuralrearrangementbysinglemoleculerealtimedetectionofreversetranscription
AT wegenerjeffrey analysisofrnabasemodificationandstructuralrearrangementbysinglemoleculerealtimedetectionofreversetranscription
AT daiqing analysisofrnabasemodificationandstructuralrearrangementbysinglemoleculerealtimedetectionofreversetranscription
AT yichengqi analysisofrnabasemodificationandstructuralrearrangementbysinglemoleculerealtimedetectionofreversetranscription
AT pantao analysisofrnabasemodificationandstructuralrearrangementbysinglemoleculerealtimedetectionofreversetranscription
AT turnerstephenw analysisofrnabasemodificationandstructuralrearrangementbysinglemoleculerealtimedetectionofreversetranscription
AT korlachjonas analysisofrnabasemodificationandstructuralrearrangementbysinglemoleculerealtimedetectionofreversetranscription