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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
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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. |
format | Online Article Text |
id | pubmed-7882013 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
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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