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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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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. |
format | Online Article Text |
id | pubmed-3973288 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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