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Peptide Nucleic Acids as a Tool for Site-Specific Gene Editing
Peptide nucleic acids (PNAs) can bind duplex DNA in a sequence-targeted manner, forming a triplex structure capable of inducing DNA repair and producing specific genome modifications. Since the first description of PNA-mediated gene editing in cell free extracts, PNAs have been used to successfully...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5946696/ https://www.ncbi.nlm.nih.gov/pubmed/29534473 http://dx.doi.org/10.3390/molecules23030632 |
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author | Ricciardi, Adele S. Quijano, Elias Putman, Rachael Saltzman, W. Mark Glazer, Peter M. |
author_facet | Ricciardi, Adele S. Quijano, Elias Putman, Rachael Saltzman, W. Mark Glazer, Peter M. |
author_sort | Ricciardi, Adele S. |
collection | PubMed |
description | Peptide nucleic acids (PNAs) can bind duplex DNA in a sequence-targeted manner, forming a triplex structure capable of inducing DNA repair and producing specific genome modifications. Since the first description of PNA-mediated gene editing in cell free extracts, PNAs have been used to successfully correct human disease-causing mutations in cell culture and in vivo in preclinical mouse models. Gene correction via PNAs has resulted in clinically-relevant functional protein restoration and disease improvement, with low off-target genome effects, indicating a strong therapeutic potential for PNAs in the treatment or cure of genetic disorders. This review discusses the progress that has been made in developing PNAs as an effective, targeted agent for gene editing, with an emphasis on recent in vivo, nanoparticle-based strategies. |
format | Online Article Text |
id | pubmed-5946696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-59466962018-05-11 Peptide Nucleic Acids as a Tool for Site-Specific Gene Editing Ricciardi, Adele S. Quijano, Elias Putman, Rachael Saltzman, W. Mark Glazer, Peter M. Molecules Review Peptide nucleic acids (PNAs) can bind duplex DNA in a sequence-targeted manner, forming a triplex structure capable of inducing DNA repair and producing specific genome modifications. Since the first description of PNA-mediated gene editing in cell free extracts, PNAs have been used to successfully correct human disease-causing mutations in cell culture and in vivo in preclinical mouse models. Gene correction via PNAs has resulted in clinically-relevant functional protein restoration and disease improvement, with low off-target genome effects, indicating a strong therapeutic potential for PNAs in the treatment or cure of genetic disorders. This review discusses the progress that has been made in developing PNAs as an effective, targeted agent for gene editing, with an emphasis on recent in vivo, nanoparticle-based strategies. MDPI 2018-03-11 /pmc/articles/PMC5946696/ /pubmed/29534473 http://dx.doi.org/10.3390/molecules23030632 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Ricciardi, Adele S. Quijano, Elias Putman, Rachael Saltzman, W. Mark Glazer, Peter M. Peptide Nucleic Acids as a Tool for Site-Specific Gene Editing |
title | Peptide Nucleic Acids as a Tool for Site-Specific Gene Editing |
title_full | Peptide Nucleic Acids as a Tool for Site-Specific Gene Editing |
title_fullStr | Peptide Nucleic Acids as a Tool for Site-Specific Gene Editing |
title_full_unstemmed | Peptide Nucleic Acids as a Tool for Site-Specific Gene Editing |
title_short | Peptide Nucleic Acids as a Tool for Site-Specific Gene Editing |
title_sort | peptide nucleic acids as a tool for site-specific gene editing |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5946696/ https://www.ncbi.nlm.nih.gov/pubmed/29534473 http://dx.doi.org/10.3390/molecules23030632 |
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