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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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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. |
format | Online Article Text |
id | pubmed-8068174 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT huntercharlest crisprcas9targetedmutagenesisforfunctionalgeneticsinmaize |