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Comparison of SHAPE reagents for mapping RNA structures inside living cells

Recent advances in SHAPE technology have converted the classic primer extension method to next-generation sequencing platforms, allowing transcriptome-level analysis of RNA secondary structure. In particular, icSHAPE and SHAPE-MaP, using NAI-N(3) and 1M7 reagents, respectively, are methods that clai...

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Autores principales: Lee, Byron, Flynn, Ryan A., Kadina, Anastasia, Guo, Jimmy K., Kool, Eric T., Chang, Howard Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5238792/
https://www.ncbi.nlm.nih.gov/pubmed/27879433
http://dx.doi.org/10.1261/rna.058784.116
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author Lee, Byron
Flynn, Ryan A.
Kadina, Anastasia
Guo, Jimmy K.
Kool, Eric T.
Chang, Howard Y.
author_facet Lee, Byron
Flynn, Ryan A.
Kadina, Anastasia
Guo, Jimmy K.
Kool, Eric T.
Chang, Howard Y.
author_sort Lee, Byron
collection PubMed
description Recent advances in SHAPE technology have converted the classic primer extension method to next-generation sequencing platforms, allowing transcriptome-level analysis of RNA secondary structure. In particular, icSHAPE and SHAPE-MaP, using NAI-N(3) and 1M7 reagents, respectively, are methods that claim to measure in vivo structure with high-throughput sequencing. However, these compounds have not been compared on an unbiased, raw-signal level. Here, we directly compare several in vivo SHAPE acylation reagents using the simple primer extension assay. We conclude that while multiple SHAPE technologies are effective at measuring purified RNAs in vitro, acylimidazole reagents NAI and NAI-N(3) give markedly greater signals with lower background than 1M7 for in vivo measurement of the RNA structurome.
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spelling pubmed-52387922017-02-01 Comparison of SHAPE reagents for mapping RNA structures inside living cells Lee, Byron Flynn, Ryan A. Kadina, Anastasia Guo, Jimmy K. Kool, Eric T. Chang, Howard Y. RNA Report Recent advances in SHAPE technology have converted the classic primer extension method to next-generation sequencing platforms, allowing transcriptome-level analysis of RNA secondary structure. In particular, icSHAPE and SHAPE-MaP, using NAI-N(3) and 1M7 reagents, respectively, are methods that claim to measure in vivo structure with high-throughput sequencing. However, these compounds have not been compared on an unbiased, raw-signal level. Here, we directly compare several in vivo SHAPE acylation reagents using the simple primer extension assay. We conclude that while multiple SHAPE technologies are effective at measuring purified RNAs in vitro, acylimidazole reagents NAI and NAI-N(3) give markedly greater signals with lower background than 1M7 for in vivo measurement of the RNA structurome. Cold Spring Harbor Laboratory Press 2017-02 /pmc/articles/PMC5238792/ /pubmed/27879433 http://dx.doi.org/10.1261/rna.058784.116 Text en © 2017 Lee et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by/4.0/ This article, published in RNA, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/.
spellingShingle Report
Lee, Byron
Flynn, Ryan A.
Kadina, Anastasia
Guo, Jimmy K.
Kool, Eric T.
Chang, Howard Y.
Comparison of SHAPE reagents for mapping RNA structures inside living cells
title Comparison of SHAPE reagents for mapping RNA structures inside living cells
title_full Comparison of SHAPE reagents for mapping RNA structures inside living cells
title_fullStr Comparison of SHAPE reagents for mapping RNA structures inside living cells
title_full_unstemmed Comparison of SHAPE reagents for mapping RNA structures inside living cells
title_short Comparison of SHAPE reagents for mapping RNA structures inside living cells
title_sort comparison of shape reagents for mapping rna structures inside living cells
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5238792/
https://www.ncbi.nlm.nih.gov/pubmed/27879433
http://dx.doi.org/10.1261/rna.058784.116
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