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Improved Somatic Mutagenesis in Zebrafish Using Transcription Activator-Like Effector Nucleases (TALENs)

Zinc Finger Nucleases (ZFNs) made by Context-Dependent Assembly (CoDA) and Transcription Activator-Like Effector Nucleases (TALENs) provide robust and user-friendly technologies for efficiently inactivating genes in zebrafish. These designer nucleases bind to and cleave DNA at particular target site...

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Autores principales: Moore, Finola E., Reyon, Deepak, Sander, Jeffry D., Martinez, Sarah A., Blackburn, Jessica S., Khayter, Cyd, Ramirez, Cherie L., Joung, J. Keith, Langenau, David M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3360007/
https://www.ncbi.nlm.nih.gov/pubmed/22655075
http://dx.doi.org/10.1371/journal.pone.0037877
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author Moore, Finola E.
Reyon, Deepak
Sander, Jeffry D.
Martinez, Sarah A.
Blackburn, Jessica S.
Khayter, Cyd
Ramirez, Cherie L.
Joung, J. Keith
Langenau, David M.
author_facet Moore, Finola E.
Reyon, Deepak
Sander, Jeffry D.
Martinez, Sarah A.
Blackburn, Jessica S.
Khayter, Cyd
Ramirez, Cherie L.
Joung, J. Keith
Langenau, David M.
author_sort Moore, Finola E.
collection PubMed
description Zinc Finger Nucleases (ZFNs) made by Context-Dependent Assembly (CoDA) and Transcription Activator-Like Effector Nucleases (TALENs) provide robust and user-friendly technologies for efficiently inactivating genes in zebrafish. These designer nucleases bind to and cleave DNA at particular target sites, inducing error-prone repair that can result in insertion or deletion mutations. Here, we assess the relative efficiencies of these technologies for inducing somatic DNA mutations in mosaic zebrafish. We find that TALENs exhibited a higher success rate for obtaining active nucleases capable of inducing mutations than compared with CoDA ZFNs. For example, all six TALENs tested induced DNA mutations at genomic target sites while only a subset of CoDA ZFNs exhibited detectable rates of mutagenesis. TALENs also exhibited higher mutation rates than CoDA ZFNs that had not been pre-screened using a bacterial two-hybrid assay, with DNA mutation rates ranging from 20%–76.8% compared to 1.1%–3.3%. Furthermore, the broader targeting range of TALENs enabled us to induce mutations at the methionine translation start site, sequences that were not targetable using the CoDA ZFN platform. TALENs exhibited similar toxicity to CoDA ZFNs, with >50% of injected animals surviving to 3 days of life. Taken together, our results suggest that TALEN technology provides a robust alternative to CoDA ZFNs for inducing targeted gene-inactivation in zebrafish, making it a preferred technology for creating targeted knockout mutants in zebrafish.
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spelling pubmed-33600072012-05-31 Improved Somatic Mutagenesis in Zebrafish Using Transcription Activator-Like Effector Nucleases (TALENs) Moore, Finola E. Reyon, Deepak Sander, Jeffry D. Martinez, Sarah A. Blackburn, Jessica S. Khayter, Cyd Ramirez, Cherie L. Joung, J. Keith Langenau, David M. PLoS One Research Article Zinc Finger Nucleases (ZFNs) made by Context-Dependent Assembly (CoDA) and Transcription Activator-Like Effector Nucleases (TALENs) provide robust and user-friendly technologies for efficiently inactivating genes in zebrafish. These designer nucleases bind to and cleave DNA at particular target sites, inducing error-prone repair that can result in insertion or deletion mutations. Here, we assess the relative efficiencies of these technologies for inducing somatic DNA mutations in mosaic zebrafish. We find that TALENs exhibited a higher success rate for obtaining active nucleases capable of inducing mutations than compared with CoDA ZFNs. For example, all six TALENs tested induced DNA mutations at genomic target sites while only a subset of CoDA ZFNs exhibited detectable rates of mutagenesis. TALENs also exhibited higher mutation rates than CoDA ZFNs that had not been pre-screened using a bacterial two-hybrid assay, with DNA mutation rates ranging from 20%–76.8% compared to 1.1%–3.3%. Furthermore, the broader targeting range of TALENs enabled us to induce mutations at the methionine translation start site, sequences that were not targetable using the CoDA ZFN platform. TALENs exhibited similar toxicity to CoDA ZFNs, with >50% of injected animals surviving to 3 days of life. Taken together, our results suggest that TALEN technology provides a robust alternative to CoDA ZFNs for inducing targeted gene-inactivation in zebrafish, making it a preferred technology for creating targeted knockout mutants in zebrafish. Public Library of Science 2012-05-24 /pmc/articles/PMC3360007/ /pubmed/22655075 http://dx.doi.org/10.1371/journal.pone.0037877 Text en Moore et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Moore, Finola E.
Reyon, Deepak
Sander, Jeffry D.
Martinez, Sarah A.
Blackburn, Jessica S.
Khayter, Cyd
Ramirez, Cherie L.
Joung, J. Keith
Langenau, David M.
Improved Somatic Mutagenesis in Zebrafish Using Transcription Activator-Like Effector Nucleases (TALENs)
title Improved Somatic Mutagenesis in Zebrafish Using Transcription Activator-Like Effector Nucleases (TALENs)
title_full Improved Somatic Mutagenesis in Zebrafish Using Transcription Activator-Like Effector Nucleases (TALENs)
title_fullStr Improved Somatic Mutagenesis in Zebrafish Using Transcription Activator-Like Effector Nucleases (TALENs)
title_full_unstemmed Improved Somatic Mutagenesis in Zebrafish Using Transcription Activator-Like Effector Nucleases (TALENs)
title_short Improved Somatic Mutagenesis in Zebrafish Using Transcription Activator-Like Effector Nucleases (TALENs)
title_sort improved somatic mutagenesis in zebrafish using transcription activator-like effector nucleases (talens)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3360007/
https://www.ncbi.nlm.nih.gov/pubmed/22655075
http://dx.doi.org/10.1371/journal.pone.0037877
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