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Advances in engineering CRISPR-Cas9 as a molecular Swiss Army knife

The RNA-guided endonuclease system CRISPR-Cas9 has been extensively modified since its discovery, allowing its capabilities to extend far beyond double-stranded cleavage to high fidelity insertions, deletions and single base edits. Such innovations have been possible due to the modular architecture...

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Detalles Bibliográficos
Autores principales: Meaker, Grace A, Hair, Emma J, Gorochowski, Thomas E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7737000/
https://www.ncbi.nlm.nih.gov/pubmed/33344779
http://dx.doi.org/10.1093/synbio/ysaa021
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author Meaker, Grace A
Hair, Emma J
Gorochowski, Thomas E
author_facet Meaker, Grace A
Hair, Emma J
Gorochowski, Thomas E
author_sort Meaker, Grace A
collection PubMed
description The RNA-guided endonuclease system CRISPR-Cas9 has been extensively modified since its discovery, allowing its capabilities to extend far beyond double-stranded cleavage to high fidelity insertions, deletions and single base edits. Such innovations have been possible due to the modular architecture of CRISPR-Cas9 and the robustness of its component parts to modifications and the fusion of new functional elements. Here, we review the broad toolkit of CRISPR-Cas9-based systems now available for diverse genome-editing tasks. We provide an overview of their core molecular structure and mechanism and distil the design principles used to engineer their diverse functionalities. We end by looking beyond the biochemistry and toward the societal and ethical challenges that these CRISPR-Cas9 systems face if their transformative capabilities are to be deployed in a safe and acceptable manner.
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spelling pubmed-77370002020-12-17 Advances in engineering CRISPR-Cas9 as a molecular Swiss Army knife Meaker, Grace A Hair, Emma J Gorochowski, Thomas E Synth Biol (Oxf) Review Article The RNA-guided endonuclease system CRISPR-Cas9 has been extensively modified since its discovery, allowing its capabilities to extend far beyond double-stranded cleavage to high fidelity insertions, deletions and single base edits. Such innovations have been possible due to the modular architecture of CRISPR-Cas9 and the robustness of its component parts to modifications and the fusion of new functional elements. Here, we review the broad toolkit of CRISPR-Cas9-based systems now available for diverse genome-editing tasks. We provide an overview of their core molecular structure and mechanism and distil the design principles used to engineer their diverse functionalities. We end by looking beyond the biochemistry and toward the societal and ethical challenges that these CRISPR-Cas9 systems face if their transformative capabilities are to be deployed in a safe and acceptable manner. Oxford University Press 2020-10-24 /pmc/articles/PMC7737000/ /pubmed/33344779 http://dx.doi.org/10.1093/synbio/ysaa021 Text en © The Author(s) 2020. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Meaker, Grace A
Hair, Emma J
Gorochowski, Thomas E
Advances in engineering CRISPR-Cas9 as a molecular Swiss Army knife
title Advances in engineering CRISPR-Cas9 as a molecular Swiss Army knife
title_full Advances in engineering CRISPR-Cas9 as a molecular Swiss Army knife
title_fullStr Advances in engineering CRISPR-Cas9 as a molecular Swiss Army knife
title_full_unstemmed Advances in engineering CRISPR-Cas9 as a molecular Swiss Army knife
title_short Advances in engineering CRISPR-Cas9 as a molecular Swiss Army knife
title_sort advances in engineering crispr-cas9 as a molecular swiss army knife
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7737000/
https://www.ncbi.nlm.nih.gov/pubmed/33344779
http://dx.doi.org/10.1093/synbio/ysaa021
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