FB2026_03 , released September 17, 2026
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Citation
Bassett, A.R., Tibbit, C., Ponting, C.P., Liu, J.L. (2013). Highly Efficient Targeted Mutagenesis of Drosophila with the CRISPR/Cas9 System.  Cell Rep. 4(1): 220--228.
FlyBase ID
FBrf0222128
Publication Type
Research paper
Abstract
Here, we present a simple and highly efficient method for generating and detecting mutations of any gene in Drosophila melanogaster through the use of the CRISPR/Cas9 system (clustered regularly interspaced palindromic repeats/CRISPR-associated). We show that injection of RNA into the Drosophila embryo can induce highly efficient mutagenesis of desired target genes in up to 88% of injected flies. These mutations can be transmitted through the germline to make stable lines. Our system provides at least a 10-fold improvement in efficiency over previously published reports, enabling wider application of this technique. We also describe a simple and highly sensitive method of detecting mutations in the target gene by high-resolution melt analysis and discuss how the new technology enables the study of gene function.
Graphical Abstract
Obtained with permission from Cell Press.
PubMed ID
PubMed Central ID
PMC3714591 (PMC) (EuropePMC)
Related Publication(s)
Erratum

Highly Efficient Targeted Mutagenesis of Drosophila with the CRISPR/Cas9 System.
Bassett et al., 2014, Cell Rep. 6(6): 1178--1179 [FBrf0250709]

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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Cell Rep.
    Title
    Cell reports
    ISBN/ISSN
    2211-1247
    Data From Reference
    Genes (2)