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CRISPR/Cas9 Targeted Mutagenesis for Functional Genetics in Maize

The CRISPR/Cas9-based system for targeted mutagenesis has become an indispensable tool for functional genetics in plants. CRISPR/Cas9 allows users to generate loss-of-function alleles in genes of interest with precision and in a simple-to-use system. This manuscript outlines important points to cons...

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Autor principal: Hunter, Charles T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8068174/
https://www.ncbi.nlm.nih.gov/pubmed/33917747
http://dx.doi.org/10.3390/plants10040723
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author Hunter, Charles T.
author_facet Hunter, Charles T.
author_sort Hunter, Charles T.
collection PubMed
description The CRISPR/Cas9-based system for targeted mutagenesis has become an indispensable tool for functional genetics in plants. CRISPR/Cas9 allows users to generate loss-of-function alleles in genes of interest with precision and in a simple-to-use system. This manuscript outlines important points to consider for experimental design and utilization of CRISPR/Cas9 in targeted mutagenesis in maize. It also introduces the pRGEB32-BAR vector modified for use in maize that allows simultaneous delivery of multiple gRNAs using a simple assembly. Vector selection, gRNA design, genetic strategies, and genotyping approaches are discussed, with an emphasis on achieving isolation of homozygous mutant plants in a time- and cost-efficient manner.
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spelling pubmed-80681742021-04-25 CRISPR/Cas9 Targeted Mutagenesis for Functional Genetics in Maize Hunter, Charles T. Plants (Basel) Communication The CRISPR/Cas9-based system for targeted mutagenesis has become an indispensable tool for functional genetics in plants. CRISPR/Cas9 allows users to generate loss-of-function alleles in genes of interest with precision and in a simple-to-use system. This manuscript outlines important points to consider for experimental design and utilization of CRISPR/Cas9 in targeted mutagenesis in maize. It also introduces the pRGEB32-BAR vector modified for use in maize that allows simultaneous delivery of multiple gRNAs using a simple assembly. Vector selection, gRNA design, genetic strategies, and genotyping approaches are discussed, with an emphasis on achieving isolation of homozygous mutant plants in a time- and cost-efficient manner. MDPI 2021-04-08 /pmc/articles/PMC8068174/ /pubmed/33917747 http://dx.doi.org/10.3390/plants10040723 Text en © 2021 by the author. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Hunter, Charles T.
CRISPR/Cas9 Targeted Mutagenesis for Functional Genetics in Maize
title CRISPR/Cas9 Targeted Mutagenesis for Functional Genetics in Maize
title_full CRISPR/Cas9 Targeted Mutagenesis for Functional Genetics in Maize
title_fullStr CRISPR/Cas9 Targeted Mutagenesis for Functional Genetics in Maize
title_full_unstemmed CRISPR/Cas9 Targeted Mutagenesis for Functional Genetics in Maize
title_short CRISPR/Cas9 Targeted Mutagenesis for Functional Genetics in Maize
title_sort crispr/cas9 targeted mutagenesis for functional genetics in maize
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8068174/
https://www.ncbi.nlm.nih.gov/pubmed/33917747
http://dx.doi.org/10.3390/plants10040723
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