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A Fast and Easy Method for Specific Detection of Circular RNA by Rolling‐Circle Amplification

Circular RNAs (circRNAs) represent a new class of usually noncoding transcripts with largely unknown functions. Their research is hampered not least by the inapplicability of traditional analytical methods. Herein we describe a rapid and easy assay for the detection of natural circRNA, based on roll...

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Detalles Bibliográficos
Autores principales: Boss, Marcel, Arenz, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154740/
https://www.ncbi.nlm.nih.gov/pubmed/31584239
http://dx.doi.org/10.1002/cbic.201900514
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author Boss, Marcel
Arenz, Christoph
author_facet Boss, Marcel
Arenz, Christoph
author_sort Boss, Marcel
collection PubMed
description Circular RNAs (circRNAs) represent a new class of usually noncoding transcripts with largely unknown functions. Their research is hampered not least by the inapplicability of traditional analytical methods. Herein we describe a rapid and easy assay for the detection of natural circRNA, based on rolling‐circle amplification (RCA). This technique does not require the use of fluorescently labeled RNA or DNA and can specifically detect circular RNA in the presence of a 1000‐fold excess of the same linear RNA. Only standard devices such as (quantitative) PCR cyclers and gel electrophoresis are used.
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spelling pubmed-71547402020-04-15 A Fast and Easy Method for Specific Detection of Circular RNA by Rolling‐Circle Amplification Boss, Marcel Arenz, Christoph Chembiochem Communications Circular RNAs (circRNAs) represent a new class of usually noncoding transcripts with largely unknown functions. Their research is hampered not least by the inapplicability of traditional analytical methods. Herein we describe a rapid and easy assay for the detection of natural circRNA, based on rolling‐circle amplification (RCA). This technique does not require the use of fluorescently labeled RNA or DNA and can specifically detect circular RNA in the presence of a 1000‐fold excess of the same linear RNA. Only standard devices such as (quantitative) PCR cyclers and gel electrophoresis are used. John Wiley and Sons Inc. 2019-11-27 2020-03-16 /pmc/articles/PMC7154740/ /pubmed/31584239 http://dx.doi.org/10.1002/cbic.201900514 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Communications
Boss, Marcel
Arenz, Christoph
A Fast and Easy Method for Specific Detection of Circular RNA by Rolling‐Circle Amplification
title A Fast and Easy Method for Specific Detection of Circular RNA by Rolling‐Circle Amplification
title_full A Fast and Easy Method for Specific Detection of Circular RNA by Rolling‐Circle Amplification
title_fullStr A Fast and Easy Method for Specific Detection of Circular RNA by Rolling‐Circle Amplification
title_full_unstemmed A Fast and Easy Method for Specific Detection of Circular RNA by Rolling‐Circle Amplification
title_short A Fast and Easy Method for Specific Detection of Circular RNA by Rolling‐Circle Amplification
title_sort fast and easy method for specific detection of circular rna by rolling‐circle amplification
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154740/
https://www.ncbi.nlm.nih.gov/pubmed/31584239
http://dx.doi.org/10.1002/cbic.201900514
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