Cargando…

Unbiased investigation of specificities of prime editing systems in human cells

Prime editors (PEs) enable targeted precise editing, including the generation of substitutions, insertions and deletions, in eukaryotic genomes. However, their genome-wide specificity has not been explored. Here, we developed Nickase-based Digenome-seq (nDigenome-seq), an in vitro assay that uses wh...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Do Yon, Moon, Su Bin, Ko, Jeong-Heon, Kim, Yong-Sam, Kim, Daesik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7544197/
https://www.ncbi.nlm.nih.gov/pubmed/32941652
http://dx.doi.org/10.1093/nar/gkaa764
_version_ 1783591810208104448
author Kim, Do Yon
Moon, Su Bin
Ko, Jeong-Heon
Kim, Yong-Sam
Kim, Daesik
author_facet Kim, Do Yon
Moon, Su Bin
Ko, Jeong-Heon
Kim, Yong-Sam
Kim, Daesik
author_sort Kim, Do Yon
collection PubMed
description Prime editors (PEs) enable targeted precise editing, including the generation of substitutions, insertions and deletions, in eukaryotic genomes. However, their genome-wide specificity has not been explored. Here, we developed Nickase-based Digenome-seq (nDigenome-seq), an in vitro assay that uses whole-genome sequencing to identify single-strand breaks induced by CRISPR (clustered regularly interspaced short palindromic repeats)-Cas9 (CRISPR-associated protein 9) nickase. We used nDigenome-seq to screen for potential genome-wide off-target sites of Cas9 H840A nickase, a PE component, targeted to nine human genomic sites. Then, using targeted amplicon sequencing of off-target candidates identified by nDigenome-seq, we showed that only five off-target sites showed detectable PE-induced modifications in cells, at frequencies ranging from 0.1 to 1.9%, suggesting that PEs provide a highly specific method of precise genome editing. We also found that PE specificity in human cells could be further improved by incorporating mutations from engineered Cas9 variants, particularly eSpCas9 and Sniper Cas9, into PE.
format Online
Article
Text
id pubmed-7544197
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-75441972020-10-15 Unbiased investigation of specificities of prime editing systems in human cells Kim, Do Yon Moon, Su Bin Ko, Jeong-Heon Kim, Yong-Sam Kim, Daesik Nucleic Acids Res Synthetic Biology and Bioengineering Prime editors (PEs) enable targeted precise editing, including the generation of substitutions, insertions and deletions, in eukaryotic genomes. However, their genome-wide specificity has not been explored. Here, we developed Nickase-based Digenome-seq (nDigenome-seq), an in vitro assay that uses whole-genome sequencing to identify single-strand breaks induced by CRISPR (clustered regularly interspaced short palindromic repeats)-Cas9 (CRISPR-associated protein 9) nickase. We used nDigenome-seq to screen for potential genome-wide off-target sites of Cas9 H840A nickase, a PE component, targeted to nine human genomic sites. Then, using targeted amplicon sequencing of off-target candidates identified by nDigenome-seq, we showed that only five off-target sites showed detectable PE-induced modifications in cells, at frequencies ranging from 0.1 to 1.9%, suggesting that PEs provide a highly specific method of precise genome editing. We also found that PE specificity in human cells could be further improved by incorporating mutations from engineered Cas9 variants, particularly eSpCas9 and Sniper Cas9, into PE. Oxford University Press 2020-09-17 /pmc/articles/PMC7544197/ /pubmed/32941652 http://dx.doi.org/10.1093/nar/gkaa764 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Synthetic Biology and Bioengineering
Kim, Do Yon
Moon, Su Bin
Ko, Jeong-Heon
Kim, Yong-Sam
Kim, Daesik
Unbiased investigation of specificities of prime editing systems in human cells
title Unbiased investigation of specificities of prime editing systems in human cells
title_full Unbiased investigation of specificities of prime editing systems in human cells
title_fullStr Unbiased investigation of specificities of prime editing systems in human cells
title_full_unstemmed Unbiased investigation of specificities of prime editing systems in human cells
title_short Unbiased investigation of specificities of prime editing systems in human cells
title_sort unbiased investigation of specificities of prime editing systems in human cells
topic Synthetic Biology and Bioengineering
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7544197/
https://www.ncbi.nlm.nih.gov/pubmed/32941652
http://dx.doi.org/10.1093/nar/gkaa764
work_keys_str_mv AT kimdoyon unbiasedinvestigationofspecificitiesofprimeeditingsystemsinhumancells
AT moonsubin unbiasedinvestigationofspecificitiesofprimeeditingsystemsinhumancells
AT kojeongheon unbiasedinvestigationofspecificitiesofprimeeditingsystemsinhumancells
AT kimyongsam unbiasedinvestigationofspecificitiesofprimeeditingsystemsinhumancells
AT kimdaesik unbiasedinvestigationofspecificitiesofprimeeditingsystemsinhumancells