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SAPTA: a new design tool for improving TALE nuclease activity

Transcription activator-like effector nucleases (TALENs) have become a powerful tool for genome editing due to the simple code linking the amino acid sequences of their DNA-binding domains to TALEN nucleotide targets. While the initial TALEN-design guidelines are very useful, user-friendly tools def...

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Detalles Bibliográficos
Autores principales: Lin, Yanni, Fine, Eli J., Zheng, Zhilan, Antico, Christopher J., Voit, Richard A., Porteus, Matthew H., Cradick, Thomas J., Bao, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973288/
https://www.ncbi.nlm.nih.gov/pubmed/24442582
http://dx.doi.org/10.1093/nar/gkt1363
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author Lin, Yanni
Fine, Eli J.
Zheng, Zhilan
Antico, Christopher J.
Voit, Richard A.
Porteus, Matthew H.
Cradick, Thomas J.
Bao, Gang
author_facet Lin, Yanni
Fine, Eli J.
Zheng, Zhilan
Antico, Christopher J.
Voit, Richard A.
Porteus, Matthew H.
Cradick, Thomas J.
Bao, Gang
author_sort Lin, Yanni
collection PubMed
description Transcription activator-like effector nucleases (TALENs) have become a powerful tool for genome editing due to the simple code linking the amino acid sequences of their DNA-binding domains to TALEN nucleotide targets. While the initial TALEN-design guidelines are very useful, user-friendly tools defining optimal TALEN designs for robust genome editing need to be developed. Here we evaluated existing guidelines and developed new design guidelines for TALENs based on 205 TALENs tested, and established the scoring algorithm for predicting TALEN activity (SAPTA) as a new online design tool. For any input gene of interest, SAPTA gives a ranked list of potential TALEN target sites, facilitating the selection of optimal TALEN pairs based on predicted activity. SAPTA-based TALEN designs increased the average intracellular TALEN monomer activity by >3-fold, and resulted in an average endogenous gene-modification frequency of 39% for TALENs containing the repeat variable di-residue NK that favors specificity rather than activity. It is expected that SAPTA will become a useful and flexible tool for designing highly active TALENs for genome-editing applications. SAPTA can be accessed via the website at http://baolab.bme.gatech.edu/Research/BioinformaticTools/TAL_targeter.html.
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spelling pubmed-39732882014-04-04 SAPTA: a new design tool for improving TALE nuclease activity Lin, Yanni Fine, Eli J. Zheng, Zhilan Antico, Christopher J. Voit, Richard A. Porteus, Matthew H. Cradick, Thomas J. Bao, Gang Nucleic Acids Res Methods Online Transcription activator-like effector nucleases (TALENs) have become a powerful tool for genome editing due to the simple code linking the amino acid sequences of their DNA-binding domains to TALEN nucleotide targets. While the initial TALEN-design guidelines are very useful, user-friendly tools defining optimal TALEN designs for robust genome editing need to be developed. Here we evaluated existing guidelines and developed new design guidelines for TALENs based on 205 TALENs tested, and established the scoring algorithm for predicting TALEN activity (SAPTA) as a new online design tool. For any input gene of interest, SAPTA gives a ranked list of potential TALEN target sites, facilitating the selection of optimal TALEN pairs based on predicted activity. SAPTA-based TALEN designs increased the average intracellular TALEN monomer activity by >3-fold, and resulted in an average endogenous gene-modification frequency of 39% for TALENs containing the repeat variable di-residue NK that favors specificity rather than activity. It is expected that SAPTA will become a useful and flexible tool for designing highly active TALENs for genome-editing applications. SAPTA can be accessed via the website at http://baolab.bme.gatech.edu/Research/BioinformaticTools/TAL_targeter.html. Oxford University Press 2014-04 2014-01-16 /pmc/articles/PMC3973288/ /pubmed/24442582 http://dx.doi.org/10.1093/nar/gkt1363 Text en © The Author(s) 2014. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), 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 Methods Online
Lin, Yanni
Fine, Eli J.
Zheng, Zhilan
Antico, Christopher J.
Voit, Richard A.
Porteus, Matthew H.
Cradick, Thomas J.
Bao, Gang
SAPTA: a new design tool for improving TALE nuclease activity
title SAPTA: a new design tool for improving TALE nuclease activity
title_full SAPTA: a new design tool for improving TALE nuclease activity
title_fullStr SAPTA: a new design tool for improving TALE nuclease activity
title_full_unstemmed SAPTA: a new design tool for improving TALE nuclease activity
title_short SAPTA: a new design tool for improving TALE nuclease activity
title_sort sapta: a new design tool for improving tale nuclease activity
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973288/
https://www.ncbi.nlm.nih.gov/pubmed/24442582
http://dx.doi.org/10.1093/nar/gkt1363
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