Cargando…

Oligonucleotide‐directed mutagenesis for precision gene editing

Differences in gene sequences, many of which are single nucleotide polymorphisms, underlie some of the most important traits in plants. With humanity facing significant challenges to increase global agricultural productivity, there is an urgent need to accelerate the development of these traits in p...

Descripción completa

Detalles Bibliográficos
Autores principales: Sauer, Noel J., Mozoruk, Jerry, Miller, Ryan B., Warburg, Zachary J., Walker, Keith A., Beetham, Peter R., Schöpke, Christian R., Gocal, Greg F. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5057361/
https://www.ncbi.nlm.nih.gov/pubmed/26503400
http://dx.doi.org/10.1111/pbi.12496
_version_ 1782459052887900160
author Sauer, Noel J.
Mozoruk, Jerry
Miller, Ryan B.
Warburg, Zachary J.
Walker, Keith A.
Beetham, Peter R.
Schöpke, Christian R.
Gocal, Greg F. W.
author_facet Sauer, Noel J.
Mozoruk, Jerry
Miller, Ryan B.
Warburg, Zachary J.
Walker, Keith A.
Beetham, Peter R.
Schöpke, Christian R.
Gocal, Greg F. W.
author_sort Sauer, Noel J.
collection PubMed
description Differences in gene sequences, many of which are single nucleotide polymorphisms, underlie some of the most important traits in plants. With humanity facing significant challenges to increase global agricultural productivity, there is an urgent need to accelerate the development of these traits in plants. oligonucleotide‐directed mutagenesis (ODM), one of the many tools of Cibus’ Rapid Trait Development System (RTDS (™)) technology, offers a rapid, precise and non‐transgenic breeding alternative for trait improvement in agriculture to address this urgent need. This review explores the application of ODM as a precision genome editing technology, with emphasis on using oligonucleotides to make targeted edits in plasmid, episomal and chromosomal DNA of bacterial, fungal, mammalian and plant systems. The process of employing ODM by way of RTDS technology has been improved in many ways by utilizing a fluorescence conversion system wherein a blue fluorescent protein (BFP) can be changed to a green fluorescent protein (GFP) by editing a single nucleotide of the BFP gene (CAC→TAC; H66 to Y66). For example, dependent on oligonucleotide length, applying oligonucleotide‐mediated technology to target the BFP transgene in Arabidopsis thaliana protoplasts resulted in up to 0.05% precisely edited GFP loci. Here, the development of traits in commercially relevant plant varieties to improve crop performance by genome editing technologies such as ODM, and by extension RTDS, is reviewed.
format Online
Article
Text
id pubmed-5057361
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-50573612016-10-19 Oligonucleotide‐directed mutagenesis for precision gene editing Sauer, Noel J. Mozoruk, Jerry Miller, Ryan B. Warburg, Zachary J. Walker, Keith A. Beetham, Peter R. Schöpke, Christian R. Gocal, Greg F. W. Plant Biotechnol J Review Articles Differences in gene sequences, many of which are single nucleotide polymorphisms, underlie some of the most important traits in plants. With humanity facing significant challenges to increase global agricultural productivity, there is an urgent need to accelerate the development of these traits in plants. oligonucleotide‐directed mutagenesis (ODM), one of the many tools of Cibus’ Rapid Trait Development System (RTDS (™)) technology, offers a rapid, precise and non‐transgenic breeding alternative for trait improvement in agriculture to address this urgent need. This review explores the application of ODM as a precision genome editing technology, with emphasis on using oligonucleotides to make targeted edits in plasmid, episomal and chromosomal DNA of bacterial, fungal, mammalian and plant systems. The process of employing ODM by way of RTDS technology has been improved in many ways by utilizing a fluorescence conversion system wherein a blue fluorescent protein (BFP) can be changed to a green fluorescent protein (GFP) by editing a single nucleotide of the BFP gene (CAC→TAC; H66 to Y66). For example, dependent on oligonucleotide length, applying oligonucleotide‐mediated technology to target the BFP transgene in Arabidopsis thaliana protoplasts resulted in up to 0.05% precisely edited GFP loci. Here, the development of traits in commercially relevant plant varieties to improve crop performance by genome editing technologies such as ODM, and by extension RTDS, is reviewed. John Wiley and Sons Inc. 2015-10-27 2016-02 /pmc/articles/PMC5057361/ /pubmed/26503400 http://dx.doi.org/10.1111/pbi.12496 Text en © 2015 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Review Articles
Sauer, Noel J.
Mozoruk, Jerry
Miller, Ryan B.
Warburg, Zachary J.
Walker, Keith A.
Beetham, Peter R.
Schöpke, Christian R.
Gocal, Greg F. W.
Oligonucleotide‐directed mutagenesis for precision gene editing
title Oligonucleotide‐directed mutagenesis for precision gene editing
title_full Oligonucleotide‐directed mutagenesis for precision gene editing
title_fullStr Oligonucleotide‐directed mutagenesis for precision gene editing
title_full_unstemmed Oligonucleotide‐directed mutagenesis for precision gene editing
title_short Oligonucleotide‐directed mutagenesis for precision gene editing
title_sort oligonucleotide‐directed mutagenesis for precision gene editing
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5057361/
https://www.ncbi.nlm.nih.gov/pubmed/26503400
http://dx.doi.org/10.1111/pbi.12496
work_keys_str_mv AT sauernoelj oligonucleotidedirectedmutagenesisforprecisiongeneediting
AT mozorukjerry oligonucleotidedirectedmutagenesisforprecisiongeneediting
AT millerryanb oligonucleotidedirectedmutagenesisforprecisiongeneediting
AT warburgzacharyj oligonucleotidedirectedmutagenesisforprecisiongeneediting
AT walkerkeitha oligonucleotidedirectedmutagenesisforprecisiongeneediting
AT beethampeterr oligonucleotidedirectedmutagenesisforprecisiongeneediting
AT schopkechristianr oligonucleotidedirectedmutagenesisforprecisiongeneediting
AT gocalgregfw oligonucleotidedirectedmutagenesisforprecisiongeneediting