bioRxiv (Cold Spring Harbor Laboratory) · 2017 · 30 citations · 18 references
Life SciencesGeneticsMolecular GeneticsGenetic EngineeringGenome EngineeringGenomicsCrispr-based EngineeringCrispr-cas SystemsGuide Rna DesignMutagenesis StrategiesRna EditingCas Nuclease EngineeringCrispr-based Genome EngineeringCrispr-cas Genome EditingDrive System DesignGenomic ControlGuide Rna FunctionNuclease-assisted Gene TargetingRna Targeting
Abstract Methods of altering wild populations are most useful when inherently limited to local geographic areas. Here we describe a novel form of gene drive based on the introduction of multiple copies of an engineered ‘daisy’ sequence into repeated elements of the genome. Each introduced copy encodes guide RNAs that target one or more engineered loci carrying the CRISPR nuclease gene and the desired traits. When organisms encoding a drive system are released into the environment, each generation of mating with wild-type organisms will reduce the average number of the guide RNA elements per ‘daisyfield’ organism by half, serving as a generational clock. The loci encoding the nuclease and payload will exhibit drive only as long as a single copy remains, placing an inherent limit on the extent of spread.
18
Valentino M. Gantz, Nijole Jasinskiene, Olga Tatarenkova et al. · Proceedings of the National Academy of Sciences · 2015 · 1K citations · Full text
Genome-wide inactivation of porcine endogenous retroviruses (PERVs)
Luhan Yang, Marc Güell, Dong Niu et al. · Science · 2015 · 619 citations · Full text