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A web tool for the design of prime-editing guide RNAs

Prime editing enables diverse genomic alterations to be written into target sites without requiring double-strand breaks or donor templates. The design of prime-editing guide RNAs (pegRNAs), which must be customized for each edit, can however be complex and time-consuming. Compared with single guide...

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Detalles Bibliográficos
Autores principales: Chow, Ryan D., Chen, Jennifer S., Shen, Johanna, Chen, Sidi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7882013/
https://www.ncbi.nlm.nih.gov/pubmed/32989284
http://dx.doi.org/10.1038/s41551-020-00622-8
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author Chow, Ryan D.
Chen, Jennifer S.
Shen, Johanna
Chen, Sidi
author_facet Chow, Ryan D.
Chen, Jennifer S.
Shen, Johanna
Chen, Sidi
author_sort Chow, Ryan D.
collection PubMed
description Prime editing enables diverse genomic alterations to be written into target sites without requiring double-strand breaks or donor templates. The design of prime-editing guide RNAs (pegRNAs), which must be customized for each edit, can however be complex and time-consuming. Compared with single guide RNAs (sgRNAs), pegRNAs have an additional 3’ extension composed of a primer binding site and a reverse-transcription template. Here, we report a web tool, which we named pegFinder (http://pegfinder.sidichenlab.org), for the rapid design of pegRNAs from reference and edited DNA sequences. pegFinder can incorporate sgRNA on-target and off-target scoring predictions into its ranking system, and nominates secondary nicking sgRNAs for increasing editing efficiency. Cas9 variants with expanded targeting ranges are also supported. To facilitate downstream experimentation, pegFinder produces a comprehensive table of candidate pegRNAs, along with oligonucleotide sequences for cloning.
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spelling pubmed-78820132021-03-28 A web tool for the design of prime-editing guide RNAs Chow, Ryan D. Chen, Jennifer S. Shen, Johanna Chen, Sidi Nat Biomed Eng Article Prime editing enables diverse genomic alterations to be written into target sites without requiring double-strand breaks or donor templates. The design of prime-editing guide RNAs (pegRNAs), which must be customized for each edit, can however be complex and time-consuming. Compared with single guide RNAs (sgRNAs), pegRNAs have an additional 3’ extension composed of a primer binding site and a reverse-transcription template. Here, we report a web tool, which we named pegFinder (http://pegfinder.sidichenlab.org), for the rapid design of pegRNAs from reference and edited DNA sequences. pegFinder can incorporate sgRNA on-target and off-target scoring predictions into its ranking system, and nominates secondary nicking sgRNAs for increasing editing efficiency. Cas9 variants with expanded targeting ranges are also supported. To facilitate downstream experimentation, pegFinder produces a comprehensive table of candidate pegRNAs, along with oligonucleotide sequences for cloning. 2020-09-28 2021-02 /pmc/articles/PMC7882013/ /pubmed/32989284 http://dx.doi.org/10.1038/s41551-020-00622-8 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Chow, Ryan D.
Chen, Jennifer S.
Shen, Johanna
Chen, Sidi
A web tool for the design of prime-editing guide RNAs
title A web tool for the design of prime-editing guide RNAs
title_full A web tool for the design of prime-editing guide RNAs
title_fullStr A web tool for the design of prime-editing guide RNAs
title_full_unstemmed A web tool for the design of prime-editing guide RNAs
title_short A web tool for the design of prime-editing guide RNAs
title_sort web tool for the design of prime-editing guide rnas
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7882013/
https://www.ncbi.nlm.nih.gov/pubmed/32989284
http://dx.doi.org/10.1038/s41551-020-00622-8
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