CRISPR/Cas9 Methodology for the Generation of Knockout Deletions in Caenorhabditis elegans
The Caenorhabditis elegans Gene Knockout Consortium is tasked with obtaining null mutations in each of the more than 20,000 open reading frames (ORFs) of this organism. To date, approximately 15,000 ORFs have associated putative null alleles. As there has been substantial success in using CRISPR/Cas...
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Online Access: | http://g3journal.org/lookup/doi/10.1534/g3.118.200778 |
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doaj-38f38c20093b4e3ab2a414f3efc289082021-07-02T09:15:02ZengOxford University PressG3: Genes, Genomes, Genetics2160-18362019-01-019113514410.1534/g3.118.20077813CRISPR/Cas9 Methodology for the Generation of Knockout Deletions in Caenorhabditis elegansVinci AuErica Li-LegerGreta RaymantStephane FlibotteGeorge ChenKiana MartinLisa FernandoClaudia DoellFederico I. RosellSu WangMark L. EdgleyAnn E. RougvieHarald HutterDonald G. MoermanThe Caenorhabditis elegans Gene Knockout Consortium is tasked with obtaining null mutations in each of the more than 20,000 open reading frames (ORFs) of this organism. To date, approximately 15,000 ORFs have associated putative null alleles. As there has been substantial success in using CRISPR/Cas9 in C. elegans, this appears to be the most promising technique to complete the task. To enhance the efficiency of using CRISPR/Cas9 to generate gene deletions in C. elegans we provide a web-based interface to access our database of guide RNAs (http://genome.sfu.ca/crispr). When coupled with previously developed selection vectors, optimization for homology arm length, and the use of purified Cas9 protein, we demonstrate a robust and effective protocol for generating deletions for this large-scale project. Debate and speculation in the larger scientific community concerning off-target effects due to non-specific Cas9 cutting has prompted us to investigate through whole genome sequencing the occurrence of single nucleotide variants and indels accompanying targeted deletions. We did not detect any off-site variants above the natural spontaneous mutation rate and therefore conclude that this modified protocol does not generate off-target events to any significant degree in C. elegans. We did, however, observe a number of non-specific alterations at the target site itself following the Cas9-induced double-strand break and offer a protocol for best practice quality control for such events.http://g3journal.org/lookup/doi/10.1534/g3.118.200778C. elegansCRISPR/Cas9homology dependent repairmutagenesis |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Vinci Au Erica Li-Leger Greta Raymant Stephane Flibotte George Chen Kiana Martin Lisa Fernando Claudia Doell Federico I. Rosell Su Wang Mark L. Edgley Ann E. Rougvie Harald Hutter Donald G. Moerman |
spellingShingle |
Vinci Au Erica Li-Leger Greta Raymant Stephane Flibotte George Chen Kiana Martin Lisa Fernando Claudia Doell Federico I. Rosell Su Wang Mark L. Edgley Ann E. Rougvie Harald Hutter Donald G. Moerman CRISPR/Cas9 Methodology for the Generation of Knockout Deletions in Caenorhabditis elegans G3: Genes, Genomes, Genetics C. elegans CRISPR/Cas9 homology dependent repair mutagenesis |
author_facet |
Vinci Au Erica Li-Leger Greta Raymant Stephane Flibotte George Chen Kiana Martin Lisa Fernando Claudia Doell Federico I. Rosell Su Wang Mark L. Edgley Ann E. Rougvie Harald Hutter Donald G. Moerman |
author_sort |
Vinci Au |
title |
CRISPR/Cas9 Methodology for the Generation of Knockout Deletions in Caenorhabditis elegans |
title_short |
CRISPR/Cas9 Methodology for the Generation of Knockout Deletions in Caenorhabditis elegans |
title_full |
CRISPR/Cas9 Methodology for the Generation of Knockout Deletions in Caenorhabditis elegans |
title_fullStr |
CRISPR/Cas9 Methodology for the Generation of Knockout Deletions in Caenorhabditis elegans |
title_full_unstemmed |
CRISPR/Cas9 Methodology for the Generation of Knockout Deletions in Caenorhabditis elegans |
title_sort |
crispr/cas9 methodology for the generation of knockout deletions in caenorhabditis elegans |
publisher |
Oxford University Press |
series |
G3: Genes, Genomes, Genetics |
issn |
2160-1836 |
publishDate |
2019-01-01 |
description |
The Caenorhabditis elegans Gene Knockout Consortium is tasked with obtaining null mutations in each of the more than 20,000 open reading frames (ORFs) of this organism. To date, approximately 15,000 ORFs have associated putative null alleles. As there has been substantial success in using CRISPR/Cas9 in C. elegans, this appears to be the most promising technique to complete the task. To enhance the efficiency of using CRISPR/Cas9 to generate gene deletions in C. elegans we provide a web-based interface to access our database of guide RNAs (http://genome.sfu.ca/crispr). When coupled with previously developed selection vectors, optimization for homology arm length, and the use of purified Cas9 protein, we demonstrate a robust and effective protocol for generating deletions for this large-scale project. Debate and speculation in the larger scientific community concerning off-target effects due to non-specific Cas9 cutting has prompted us to investigate through whole genome sequencing the occurrence of single nucleotide variants and indels accompanying targeted deletions. We did not detect any off-site variants above the natural spontaneous mutation rate and therefore conclude that this modified protocol does not generate off-target events to any significant degree in C. elegans. We did, however, observe a number of non-specific alterations at the target site itself following the Cas9-induced double-strand break and offer a protocol for best practice quality control for such events. |
topic |
C. elegans CRISPR/Cas9 homology dependent repair mutagenesis |
url |
http://g3journal.org/lookup/doi/10.1534/g3.118.200778 |
work_keys_str_mv |
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