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Engineered prime editors with PAM flexibility

Although prime editors are a powerful tool for genome editing, which can generate various types of mutations such as nucleotide substitutions, insertions, and deletions in the genome without double-strand breaks or donor DNA, the conventional prime editors are still limited to their target scopes be...

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Autores principales: Kweon, Jiyeon, Yoon, Jung-Ki, Jang, An-Hee, Shin, Ha Rim, See, Ji-Eun, Jang, Gayoung, Kim, Jong-Il, Kim, Yongsub
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8178456/
https://www.ncbi.nlm.nih.gov/pubmed/33636398
http://dx.doi.org/10.1016/j.ymthe.2021.02.022
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author Kweon, Jiyeon
Yoon, Jung-Ki
Jang, An-Hee
Shin, Ha Rim
See, Ji-Eun
Jang, Gayoung
Kim, Jong-Il
Kim, Yongsub
author_facet Kweon, Jiyeon
Yoon, Jung-Ki
Jang, An-Hee
Shin, Ha Rim
See, Ji-Eun
Jang, Gayoung
Kim, Jong-Il
Kim, Yongsub
author_sort Kweon, Jiyeon
collection PubMed
description Although prime editors are a powerful tool for genome editing, which can generate various types of mutations such as nucleotide substitutions, insertions, and deletions in the genome without double-strand breaks or donor DNA, the conventional prime editors are still limited to their target scopes because of the PAM preference of the Streptococcus pyogenes Cas9 (spCas9) protein. Here, we describe the engineered prime editors to expand the range of their target sites using various PAM-flexible Cas9 variants. Using the engineered prime editors, we could successfully generate more than 50 types of mutations with up to 51.7% prime-editing activity in HEK293T cells. In addition, we successfully introduced the BRAF V600E mutation, which could not be induced by conventional prime editors. These variants of prime editors will broaden the applicability of CRISPR-based prime editing technologies in biological research.
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spelling pubmed-81784562022-06-02 Engineered prime editors with PAM flexibility Kweon, Jiyeon Yoon, Jung-Ki Jang, An-Hee Shin, Ha Rim See, Ji-Eun Jang, Gayoung Kim, Jong-Il Kim, Yongsub Mol Ther Original Article Although prime editors are a powerful tool for genome editing, which can generate various types of mutations such as nucleotide substitutions, insertions, and deletions in the genome without double-strand breaks or donor DNA, the conventional prime editors are still limited to their target scopes because of the PAM preference of the Streptococcus pyogenes Cas9 (spCas9) protein. Here, we describe the engineered prime editors to expand the range of their target sites using various PAM-flexible Cas9 variants. Using the engineered prime editors, we could successfully generate more than 50 types of mutations with up to 51.7% prime-editing activity in HEK293T cells. In addition, we successfully introduced the BRAF V600E mutation, which could not be induced by conventional prime editors. These variants of prime editors will broaden the applicability of CRISPR-based prime editing technologies in biological research. American Society of Gene & Cell Therapy 2021-06-02 2021-02-24 /pmc/articles/PMC8178456/ /pubmed/33636398 http://dx.doi.org/10.1016/j.ymthe.2021.02.022 Text en © 2021 The Author(s) https://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 Original Article
Kweon, Jiyeon
Yoon, Jung-Ki
Jang, An-Hee
Shin, Ha Rim
See, Ji-Eun
Jang, Gayoung
Kim, Jong-Il
Kim, Yongsub
Engineered prime editors with PAM flexibility
title Engineered prime editors with PAM flexibility
title_full Engineered prime editors with PAM flexibility
title_fullStr Engineered prime editors with PAM flexibility
title_full_unstemmed Engineered prime editors with PAM flexibility
title_short Engineered prime editors with PAM flexibility
title_sort engineered prime editors with pam flexibility
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8178456/
https://www.ncbi.nlm.nih.gov/pubmed/33636398
http://dx.doi.org/10.1016/j.ymthe.2021.02.022
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