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The FusX TALE Base Editor (FusXTBE) for Rapid Mitochondrial DNA Programming of Human Cells In Vitro and Zebrafish Disease Models In Vivo

Functional analyses of mitochondria have been hampered by few effective approaches to manipulate mitochondrial DNA (mtDNA) and a lack of existing animal models. Recently a TALE-derived base editor was shown to induce C-to-T (or G-to-A) sequence changes in mtDNA. We report here the FusX TALE Base Edi...

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Autores principales: Sabharwal, Ankit, Kar, Bibekananda, Restrepo-Castillo, Santiago, Holmberg, Shannon R., Mathew, Neal D., Kendall, Benjamin Luke, Cotter, Ryan P., WareJoncas, Zachary, Seiler, Christoph, Nakamaru-Ogiso, Eiko, Clark, Karl J., Ekker, Stephen C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc., publishers 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8742272/
https://www.ncbi.nlm.nih.gov/pubmed/34847747
http://dx.doi.org/10.1089/crispr.2021.0061
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author Sabharwal, Ankit
Kar, Bibekananda
Restrepo-Castillo, Santiago
Holmberg, Shannon R.
Mathew, Neal D.
Kendall, Benjamin Luke
Cotter, Ryan P.
WareJoncas, Zachary
Seiler, Christoph
Nakamaru-Ogiso, Eiko
Clark, Karl J.
Ekker, Stephen C.
author_facet Sabharwal, Ankit
Kar, Bibekananda
Restrepo-Castillo, Santiago
Holmberg, Shannon R.
Mathew, Neal D.
Kendall, Benjamin Luke
Cotter, Ryan P.
WareJoncas, Zachary
Seiler, Christoph
Nakamaru-Ogiso, Eiko
Clark, Karl J.
Ekker, Stephen C.
author_sort Sabharwal, Ankit
collection PubMed
description Functional analyses of mitochondria have been hampered by few effective approaches to manipulate mitochondrial DNA (mtDNA) and a lack of existing animal models. Recently a TALE-derived base editor was shown to induce C-to-T (or G-to-A) sequence changes in mtDNA. We report here the FusX TALE Base Editor (FusXTBE) to facilitate broad-based access to TALE mitochondrial base editing technology. TALE Writer is a de novo in silico design tool to map potential mtDNA base editing sites. FusXTBE was demonstrated to function with comparable activity to the initial base editor in human cells in vitro. Zebrafish embryos were used as a pioneering in vivo test system, with FusXTBE inducing 90+% editing efficiency in mtDNA loci as an example of near-complete induction of mtDNA heteroplasmy in vivo. Gene editing specificity as precise as a single nucleotide was observed for a protein-coding gene. Nondestructive genotyping enables single-animal mtDNA analyses for downstream biological functional genomic applications. FusXTBE is a new gene editing toolkit for exploring important questions in mitochondrial biology and genetics.
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spelling pubmed-87422722022-01-10 The FusX TALE Base Editor (FusXTBE) for Rapid Mitochondrial DNA Programming of Human Cells In Vitro and Zebrafish Disease Models In Vivo Sabharwal, Ankit Kar, Bibekananda Restrepo-Castillo, Santiago Holmberg, Shannon R. Mathew, Neal D. Kendall, Benjamin Luke Cotter, Ryan P. WareJoncas, Zachary Seiler, Christoph Nakamaru-Ogiso, Eiko Clark, Karl J. Ekker, Stephen C. CRISPR J Research Articles Functional analyses of mitochondria have been hampered by few effective approaches to manipulate mitochondrial DNA (mtDNA) and a lack of existing animal models. Recently a TALE-derived base editor was shown to induce C-to-T (or G-to-A) sequence changes in mtDNA. We report here the FusX TALE Base Editor (FusXTBE) to facilitate broad-based access to TALE mitochondrial base editing technology. TALE Writer is a de novo in silico design tool to map potential mtDNA base editing sites. FusXTBE was demonstrated to function with comparable activity to the initial base editor in human cells in vitro. Zebrafish embryos were used as a pioneering in vivo test system, with FusXTBE inducing 90+% editing efficiency in mtDNA loci as an example of near-complete induction of mtDNA heteroplasmy in vivo. Gene editing specificity as precise as a single nucleotide was observed for a protein-coding gene. Nondestructive genotyping enables single-animal mtDNA analyses for downstream biological functional genomic applications. FusXTBE is a new gene editing toolkit for exploring important questions in mitochondrial biology and genetics. Mary Ann Liebert, Inc., publishers 2021-12-01 2021-12-16 /pmc/articles/PMC8742272/ /pubmed/34847747 http://dx.doi.org/10.1089/crispr.2021.0061 Text en © Ankit Sabharwal, et al. 2021; Published by Mary Ann Liebert, Inc. https://creativecommons.org/licenses/by-nc/4.0/This Open Access article is distributed under the terms of the Creative Commons Attribution Noncommercial License [CC-BY-NC] (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are cited.
spellingShingle Research Articles
Sabharwal, Ankit
Kar, Bibekananda
Restrepo-Castillo, Santiago
Holmberg, Shannon R.
Mathew, Neal D.
Kendall, Benjamin Luke
Cotter, Ryan P.
WareJoncas, Zachary
Seiler, Christoph
Nakamaru-Ogiso, Eiko
Clark, Karl J.
Ekker, Stephen C.
The FusX TALE Base Editor (FusXTBE) for Rapid Mitochondrial DNA Programming of Human Cells In Vitro and Zebrafish Disease Models In Vivo
title The FusX TALE Base Editor (FusXTBE) for Rapid Mitochondrial DNA Programming of Human Cells In Vitro and Zebrafish Disease Models In Vivo
title_full The FusX TALE Base Editor (FusXTBE) for Rapid Mitochondrial DNA Programming of Human Cells In Vitro and Zebrafish Disease Models In Vivo
title_fullStr The FusX TALE Base Editor (FusXTBE) for Rapid Mitochondrial DNA Programming of Human Cells In Vitro and Zebrafish Disease Models In Vivo
title_full_unstemmed The FusX TALE Base Editor (FusXTBE) for Rapid Mitochondrial DNA Programming of Human Cells In Vitro and Zebrafish Disease Models In Vivo
title_short The FusX TALE Base Editor (FusXTBE) for Rapid Mitochondrial DNA Programming of Human Cells In Vitro and Zebrafish Disease Models In Vivo
title_sort fusx tale base editor (fusxtbe) for rapid mitochondrial dna programming of human cells in vitro and zebrafish disease models in vivo
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8742272/
https://www.ncbi.nlm.nih.gov/pubmed/34847747
http://dx.doi.org/10.1089/crispr.2021.0061
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