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Protocol for High-Resolution Mapping of Splicing Products and Isoforms by RT-PCR Using Fluorescently Labeled Primers

We describe an RT-PCR protocol that allows high-resolution mapping of splicing products and isoforms using fluorescently labeled primers. Each species contains one fluorescent group allowing a direct comparison of the different isoforms despite size differences. A custom-size ladder enables the prec...

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Detalles Bibliográficos
Autores principales: Weathers, Indya, Gabunilas, Jason, Samson, Joyce, Roy, Kevin, Chanfreau, Guillaume F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757285/
https://www.ncbi.nlm.nih.gov/pubmed/33377034
http://dx.doi.org/10.1016/j.xpro.2020.100140
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author Weathers, Indya
Gabunilas, Jason
Samson, Joyce
Roy, Kevin
Chanfreau, Guillaume F.
author_facet Weathers, Indya
Gabunilas, Jason
Samson, Joyce
Roy, Kevin
Chanfreau, Guillaume F.
author_sort Weathers, Indya
collection PubMed
description We describe an RT-PCR protocol that allows high-resolution mapping of splicing products and isoforms using fluorescently labeled primers. Each species contains one fluorescent group allowing a direct comparison of the different isoforms despite size differences. A custom-size ladder enables the precise determination of cDNA lengths and discrimination of isoforms differing by less than five nucleotides on polyacrylamide gels. This protocol also allows the detection of products from in vitro splicing reactions, circumventing the need to use radiolabeled transcripts. For complete details on the use and execution of this protocol, please refer to Gabunilas and Chanfreau (2016).
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spelling pubmed-77572852020-12-28 Protocol for High-Resolution Mapping of Splicing Products and Isoforms by RT-PCR Using Fluorescently Labeled Primers Weathers, Indya Gabunilas, Jason Samson, Joyce Roy, Kevin Chanfreau, Guillaume F. STAR Protoc Protocol We describe an RT-PCR protocol that allows high-resolution mapping of splicing products and isoforms using fluorescently labeled primers. Each species contains one fluorescent group allowing a direct comparison of the different isoforms despite size differences. A custom-size ladder enables the precise determination of cDNA lengths and discrimination of isoforms differing by less than five nucleotides on polyacrylamide gels. This protocol also allows the detection of products from in vitro splicing reactions, circumventing the need to use radiolabeled transcripts. For complete details on the use and execution of this protocol, please refer to Gabunilas and Chanfreau (2016). Elsevier 2020-10-21 /pmc/articles/PMC7757285/ /pubmed/33377034 http://dx.doi.org/10.1016/j.xpro.2020.100140 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Weathers, Indya
Gabunilas, Jason
Samson, Joyce
Roy, Kevin
Chanfreau, Guillaume F.
Protocol for High-Resolution Mapping of Splicing Products and Isoforms by RT-PCR Using Fluorescently Labeled Primers
title Protocol for High-Resolution Mapping of Splicing Products and Isoforms by RT-PCR Using Fluorescently Labeled Primers
title_full Protocol for High-Resolution Mapping of Splicing Products and Isoforms by RT-PCR Using Fluorescently Labeled Primers
title_fullStr Protocol for High-Resolution Mapping of Splicing Products and Isoforms by RT-PCR Using Fluorescently Labeled Primers
title_full_unstemmed Protocol for High-Resolution Mapping of Splicing Products and Isoforms by RT-PCR Using Fluorescently Labeled Primers
title_short Protocol for High-Resolution Mapping of Splicing Products and Isoforms by RT-PCR Using Fluorescently Labeled Primers
title_sort protocol for high-resolution mapping of splicing products and isoforms by rt-pcr using fluorescently labeled primers
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757285/
https://www.ncbi.nlm.nih.gov/pubmed/33377034
http://dx.doi.org/10.1016/j.xpro.2020.100140
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