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A novel Cas9 fusion protein promotes targeted genome editing with reduced mutational burden in primary human cells

Precise genome editing requires the resolution of nuclease-induced DNA double strand breaks (DSBs) via the homology-directed repair (HDR) pathway. In mammals, this is typically outcompeted by non-homologous end-joining (NHEJ) that can generate potentially genotoxic insertion/deletion mutations at DS...

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Autores principales: Carusillo, Antonio, Haider, Sibtain, Schäfer, Raul, Rhiel, Manuel, Türk, Daniel, Chmielewski, Kay O, Klermund, Julia, Mosti, Laura, Andrieux, Geoffroy, Schäfer, Richard, Cornu, Tatjana I, Cathomen, Toni, Mussolino, Claudio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10201422/
https://www.ncbi.nlm.nih.gov/pubmed/37070192
http://dx.doi.org/10.1093/nar/gkad255
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author Carusillo, Antonio
Haider, Sibtain
Schäfer, Raul
Rhiel, Manuel
Türk, Daniel
Chmielewski, Kay O
Klermund, Julia
Mosti, Laura
Andrieux, Geoffroy
Schäfer, Richard
Cornu, Tatjana I
Cathomen, Toni
Mussolino, Claudio
author_facet Carusillo, Antonio
Haider, Sibtain
Schäfer, Raul
Rhiel, Manuel
Türk, Daniel
Chmielewski, Kay O
Klermund, Julia
Mosti, Laura
Andrieux, Geoffroy
Schäfer, Richard
Cornu, Tatjana I
Cathomen, Toni
Mussolino, Claudio
author_sort Carusillo, Antonio
collection PubMed
description Precise genome editing requires the resolution of nuclease-induced DNA double strand breaks (DSBs) via the homology-directed repair (HDR) pathway. In mammals, this is typically outcompeted by non-homologous end-joining (NHEJ) that can generate potentially genotoxic insertion/deletion mutations at DSB sites. Because of higher efficacy, clinical genome editing has been restricted to imperfect but efficient NHEJ-based approaches. Hence, strategies that promote DSB resolution via HDR are essential to facilitate clinical transition of HDR-based editing strategies and increase safety. Here we describe a novel platform that consists of a Cas9 fused to DNA repair factors to synergistically inhibit NHEJ and favor HDR for precise repairing of Cas-induced DSBs. Compared to canonical CRISPR/Cas9, the increase in error-free editing ranges from 1.5-fold to 7-fold in multiple cell lines and in primary human cells. This novel CRISPR/Cas9 platform accepts clinically relevant repair templates, such as oligodeoxynucleotides (ODNs) and adeno-associated virus (AAV)-based vectors, and has a lower propensity to induce chromosomal translocations as compared to benchmark CRISPR/Cas9. The observed reduced mutational burden, resulting from diminished indel formation at on- and off-target sites, provides a remarkable gain in safety and advocates this novel CRISPR system as an attractive tool for therapeutic applications depending on precision genome editing.
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spelling pubmed-102014222023-05-23 A novel Cas9 fusion protein promotes targeted genome editing with reduced mutational burden in primary human cells Carusillo, Antonio Haider, Sibtain Schäfer, Raul Rhiel, Manuel Türk, Daniel Chmielewski, Kay O Klermund, Julia Mosti, Laura Andrieux, Geoffroy Schäfer, Richard Cornu, Tatjana I Cathomen, Toni Mussolino, Claudio Nucleic Acids Res Synthetic Biology and Bioengineering Precise genome editing requires the resolution of nuclease-induced DNA double strand breaks (DSBs) via the homology-directed repair (HDR) pathway. In mammals, this is typically outcompeted by non-homologous end-joining (NHEJ) that can generate potentially genotoxic insertion/deletion mutations at DSB sites. Because of higher efficacy, clinical genome editing has been restricted to imperfect but efficient NHEJ-based approaches. Hence, strategies that promote DSB resolution via HDR are essential to facilitate clinical transition of HDR-based editing strategies and increase safety. Here we describe a novel platform that consists of a Cas9 fused to DNA repair factors to synergistically inhibit NHEJ and favor HDR for precise repairing of Cas-induced DSBs. Compared to canonical CRISPR/Cas9, the increase in error-free editing ranges from 1.5-fold to 7-fold in multiple cell lines and in primary human cells. This novel CRISPR/Cas9 platform accepts clinically relevant repair templates, such as oligodeoxynucleotides (ODNs) and adeno-associated virus (AAV)-based vectors, and has a lower propensity to induce chromosomal translocations as compared to benchmark CRISPR/Cas9. The observed reduced mutational burden, resulting from diminished indel formation at on- and off-target sites, provides a remarkable gain in safety and advocates this novel CRISPR system as an attractive tool for therapeutic applications depending on precision genome editing. Oxford University Press 2023-04-18 /pmc/articles/PMC10201422/ /pubmed/37070192 http://dx.doi.org/10.1093/nar/gkad255 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://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
Carusillo, Antonio
Haider, Sibtain
Schäfer, Raul
Rhiel, Manuel
Türk, Daniel
Chmielewski, Kay O
Klermund, Julia
Mosti, Laura
Andrieux, Geoffroy
Schäfer, Richard
Cornu, Tatjana I
Cathomen, Toni
Mussolino, Claudio
A novel Cas9 fusion protein promotes targeted genome editing with reduced mutational burden in primary human cells
title A novel Cas9 fusion protein promotes targeted genome editing with reduced mutational burden in primary human cells
title_full A novel Cas9 fusion protein promotes targeted genome editing with reduced mutational burden in primary human cells
title_fullStr A novel Cas9 fusion protein promotes targeted genome editing with reduced mutational burden in primary human cells
title_full_unstemmed A novel Cas9 fusion protein promotes targeted genome editing with reduced mutational burden in primary human cells
title_short A novel Cas9 fusion protein promotes targeted genome editing with reduced mutational burden in primary human cells
title_sort novel cas9 fusion protein promotes targeted genome editing with reduced mutational burden in primary human cells
topic Synthetic Biology and Bioengineering
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10201422/
https://www.ncbi.nlm.nih.gov/pubmed/37070192
http://dx.doi.org/10.1093/nar/gkad255
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