Genetic modification enables modification of target genes or genome structure in livestock and experimental animals. These technologies have not only advanced bioscience but also improved agricultural productivity. To introduce a foreign transgene, the piggyBac transposon element/transposase system could be used for production of transgenic animals and specific target protein-expressing animal cells. In addition, the CRISPR-Cas9 (clustered regularly interspaced short palindromic repeat-CRISPR associated protein 9) system have been utilized to generate chickens with knockout of G0S2 (G0/G1 switch gene 2) and myostatin, which are related to lipid deposition and muscle growth, respectively. These experimental chickens could be the invaluable genetic resources to investigate the regulatory pathways and mechanisms of improvement of economic traits such as fat quantity and growth. The geneedited animals could also be applicable to the livestock industry.
Gene-editing systems
Homologous recombination gene targeting technologyTo modify genes or genome structure by knockout of a target gene or its knockin to a locus, gene targeting by homologous recombination is used [1-5]. Homologous recombination enables exchange of genetic information between genomic and exogenous donor templates via crossover events [1]. Combining pluripotent embryonic stem (ES) cells with gene targeting technology has provided insight into gene functions and regulatory mechanisms by enabling the development of knock-out or -in animal models [1-5]. In 1989, mice with knockout of hypoxanthine phosphoribosyltransferase (HPRT), β2-microglobulin, and c-abl were generated by germline transmission of knockout ES cells [1-4]. Thereafter, many studies based on homologous recombination for industrial applications and basic research have been published