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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Main Authors: 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
Format: Article
Language:English
Published: Oxford University Press 2019-01-01
Series:G3: Genes, Genomes, Genetics
Subjects:
Online Access:http://g3journal.org/lookup/doi/10.1534/g3.118.200778
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spelling 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
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