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CRISPR-Cas immunity, DNA repair and genome stability

Co-opting of CRISPR-Cas ‘Interference’ reactions for editing the genomes of eukaryotic and prokaryotic cells has highlighted crucial support roles for DNA repair systems that strive to maintain genome stability. As front-runners in genome editing that targets DNA, the class 2 CRISPR-Cas enzymes Cas9...

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Detalles Bibliográficos
Autores principales: Cubbon, Andrew, Ivancic-Bace, Ivana, Bolt, Edward L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147917/
https://www.ncbi.nlm.nih.gov/pubmed/30209206
http://dx.doi.org/10.1042/BSR20180457
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author Cubbon, Andrew
Ivancic-Bace, Ivana
Bolt, Edward L.
author_facet Cubbon, Andrew
Ivancic-Bace, Ivana
Bolt, Edward L.
author_sort Cubbon, Andrew
collection PubMed
description Co-opting of CRISPR-Cas ‘Interference’ reactions for editing the genomes of eukaryotic and prokaryotic cells has highlighted crucial support roles for DNA repair systems that strive to maintain genome stability. As front-runners in genome editing that targets DNA, the class 2 CRISPR-Cas enzymes Cas9 and Cas12a rely on repair of DNA double-strand breaks (DDSBs) by host DNA repair enzymes, using mechanisms that vary in how well they are understood. Data are emerging about the identities of DNA repair enzymes that support genome editing in human cells. At the same time, it is becoming apparent that CRISPR-Cas systems functioning in their native environment, bacteria or archaea, also need DNA repair enzymes. In this short review, we survey how DNA repair and CRISPR-Cas systems are intertwined. We consider how understanding DNA repair and CRISPR-Cas interference reactions in nature might help improve the efficacy of genome editing procedures that utilise homologous or analogous systems in human and other cells.
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spelling pubmed-61479172018-09-25 CRISPR-Cas immunity, DNA repair and genome stability Cubbon, Andrew Ivancic-Bace, Ivana Bolt, Edward L. Biosci Rep Review Articles Co-opting of CRISPR-Cas ‘Interference’ reactions for editing the genomes of eukaryotic and prokaryotic cells has highlighted crucial support roles for DNA repair systems that strive to maintain genome stability. As front-runners in genome editing that targets DNA, the class 2 CRISPR-Cas enzymes Cas9 and Cas12a rely on repair of DNA double-strand breaks (DDSBs) by host DNA repair enzymes, using mechanisms that vary in how well they are understood. Data are emerging about the identities of DNA repair enzymes that support genome editing in human cells. At the same time, it is becoming apparent that CRISPR-Cas systems functioning in their native environment, bacteria or archaea, also need DNA repair enzymes. In this short review, we survey how DNA repair and CRISPR-Cas systems are intertwined. We consider how understanding DNA repair and CRISPR-Cas interference reactions in nature might help improve the efficacy of genome editing procedures that utilise homologous or analogous systems in human and other cells. Portland Press Ltd. 2018-09-21 /pmc/articles/PMC6147917/ /pubmed/30209206 http://dx.doi.org/10.1042/BSR20180457 Text en © 2018 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review Articles
Cubbon, Andrew
Ivancic-Bace, Ivana
Bolt, Edward L.
CRISPR-Cas immunity, DNA repair and genome stability
title CRISPR-Cas immunity, DNA repair and genome stability
title_full CRISPR-Cas immunity, DNA repair and genome stability
title_fullStr CRISPR-Cas immunity, DNA repair and genome stability
title_full_unstemmed CRISPR-Cas immunity, DNA repair and genome stability
title_short CRISPR-Cas immunity, DNA repair and genome stability
title_sort crispr-cas immunity, dna repair and genome stability
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147917/
https://www.ncbi.nlm.nih.gov/pubmed/30209206
http://dx.doi.org/10.1042/BSR20180457
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