학술논문

Reproducibility of CRISPR-Cas9 methods for generation of conditional mouse alleles: a multi-center evaluation
Document Type
article
Author
Gurumurthy, Channabasavaiah BO’Brien, Aidan RQuadros, Rolen MAdams, JohnAlcaide, PilarAyabe, ShinyaBallard, JohnathanBatra, Surinder KBeauchamp, Marie-ClaudeBecker, Kathleen ABernas, GuillaumeBrough, DavidCarrillo-Salinas, FranciscoChan, WesleyChen, HanyingDawson, RubyDeMambro, VictoriaD’Hont, JinkeDibb, Katharine MEudy, James DGan, LinGao, JingGonzales, AmyGuntur, Anyonya RGuo, HuipingHarms, Donald WHarrington, AnneHentges, Kathryn EHumphreys, NeilImai, ShihoIshii, HideshiIwama, MizuhoJonasch, EricKarolak, MichelleKeavney, BernardKhin, Nay-ChiKonno, MasamitsuKotani, YukoKunihiro, YayoiLakshmanan, ImayavarambanLarochelle, CatherineLawrence, Catherine BLi, LinLindner, VolkhardLiu, Xian-DeLopez-Castejon, GloriaLoudon, AndrewLowe, JennaJerome-Majewska, Loydie AMatsusaka, TaijiMiura, HiromiMiyasaka, YoshikiMorpurgo, BenjaminMotyl, KatherineNabeshima, Yo-ichiNakade, KojiNakashiba, ToshiakiNakashima, KenichiObata, YuichiOgiwara, SanaeOuellet, MarietteOxburgh, LeifPiltz, SandraPinz, IlkaPonnusamy, Moorthy PRay, DavidRedder, Ronald JRosen, Clifford JRoss, NikkiRuhe, Mark TRyzhova, LarisaSalvador, Ane MAlam, Sabrina ShameenSedlacek, RadislavSharma, KaranSmith, ChadStaes, KatrienStarrs, LoraSugiyama, FumihiroTakahashi, SatoruTanaka, TomohiroTrafford, Andrew WUno, YoshihiroVanhoutte, LeenVanrockeghem, FrederiqueWillis, Brandon JWright, Christian SYamauchi, YukoYi, XinYoshimi, KazutoZhang, XuesongZhang, YuOhtsuka, MasatoDas, SatyabrataGarry, Daniel JHochepied, TinoThomas, PaulParker-Thornburg, JanAdamson, Antony DYoshiki, Atsushi
Source
Genome Biology. 20(1)
Subject
Biological Sciences
Genetics
Biotechnology
Prevention
Alleles
Animals
Blastocyst
CRISPR-Associated Protein 9
CRISPR-Cas Systems
Factor Analysis
Statistical
Female
Male
Methyl-CpG-Binding Protein 2
Mice
Knockout
Microinjections
Regression Analysis
Reproducibility of Results
CRISPR-Cas9
Mouse
Transgenesis
Homology-directed repair
Conditional knockout mouse
Floxed allele
Oligonucleotide
Long single-stranded DNA
Machine learning
Reproducibility
Environmental Sciences
Information and Computing Sciences
Bioinformatics
Language
Abstract
BackgroundCRISPR-Cas9 gene-editing technology has facilitated the generation of knockout mice, providing an alternative to cumbersome and time-consuming traditional embryonic stem cell-based methods. An earlier study reported up to 16% efficiency in generating conditional knockout (cKO or floxed) alleles by microinjection of 2 single guide RNAs (sgRNA) and 2 single-stranded oligonucleotides as donors (referred herein as "two-donor floxing" method).ResultsWe re-evaluate the two-donor method from a consortium of 20 laboratories across the world. The dataset constitutes 56 genetic loci, 17,887 zygotes, and 1718 live-born mice, of which only 15 (0.87%) mice contain cKO alleles. We subject the dataset to statistical analyses and a machine learning algorithm, which reveals that none of the factors analyzed was predictive for the success of this method. We test some of the newer methods that use one-donor DNA on 18 loci for which the two-donor approach failed to produce cKO alleles. We find that the one-donor methods are 10- to 20-fold more efficient than the two-donor approach.ConclusionWe propose that the two-donor method lacks efficiency because it relies on two simultaneous recombination events in cis, an outcome that is dwarfed by pervasive accompanying undesired editing events. The methods that use one-donor DNA are fairly efficient as they rely on only one recombination event, and the probability of correct insertion of the donor cassette without unanticipated mutational events is much higher. Therefore, one-donor methods offer higher efficiencies for the routine generation of cKO animal models.