Your browser doesn't support javascript.
loading
Bombyx mori kynurenine 3-monooxygenase gene editing and insect molecular breeding using the clustered regularly interspaced short palindromic repeat/CRISPR associated protein 9 system.
Hong, Jeong Won; Jeong, Chan Young; Yu, Jeong Hee; Kim, Su-Bae; Kang, Sang Kuk; Kim, Seong-Wan; Kim, Nam-Suk; Kim, Kee Young; Park, Jong Woo.
Afiliación
  • Hong JW; Department of Agricultural Biology, National Institute of Agricultural Sciences, Wanju-gun, Jeollabuk-do, Republic of Korea.
  • Jeong CY; Department of Agricultural Biology, National Institute of Agricultural Sciences, Wanju-gun, Jeollabuk-do, Republic of Korea.
  • Yu JH; Department of Agricultural Biology, National Institute of Agricultural Sciences, Wanju-gun, Jeollabuk-do, Republic of Korea.
  • Kim SB; Department of Agricultural Biology, National Institute of Agricultural Sciences, Wanju-gun, Jeollabuk-do, Republic of Korea.
  • Kang SK; Department of Agricultural Biology, National Institute of Agricultural Sciences, Wanju-gun, Jeollabuk-do, Republic of Korea.
  • Kim SW; Department of Agricultural Biology, National Institute of Agricultural Sciences, Wanju-gun, Jeollabuk-do, Republic of Korea.
  • Kim NS; Department of Agricultural Biology, National Institute of Agricultural Sciences, Wanju-gun, Jeollabuk-do, Republic of Korea.
  • Kim KY; Department of Agricultural Biology, National Institute of Agricultural Sciences, Wanju-gun, Jeollabuk-do, Republic of Korea.
  • Park JW; Department of Agricultural Biology, National Institute of Agricultural Sciences, Wanju-gun, Jeollabuk-do, Republic of Korea.
Biotechnol Prog ; 36(6): e3054, 2020 11.
Article en En | MEDLINE | ID: mdl-32706513
Genome editing by clustered regularly interspaced short palindromic repeat (CRISPR)/CRISPR associated protein (Cas)9, a third-generation gene scissors, and molecular breeding at the genome level are attracting considerable attention as future breeding techniques. In the present study, genetic and phenotypic analyses were conducted to examine the molecular breeding of Bombyx mori through CRISPR/Cas9-mediated editing of the kynurenine 3-monooxygenase (KMO) gene. The synthesized guide RNAs (gRNAs) were analyzed using T7 endonuclease I after introduction into the BM-N silkworm cell line. To edit the silkworm gene, K1P gRNA, and Cas9 complexes were microinjected into silkworm embryos. After microinjection, the hatching rate and the incidence of mutation were determined as 18.1% and 60%, respectively. Gene mutation was verified in the heterozygous G0 generation, but no phenotypic change was observed; however, certain embryos and moths produced through sib-mating had significant differences compared to the wild-type. In successive generations, a distinct phenotypic change was also observed by continuous mating. Thus, although there are limitations in the phenotypic expression in breeding through the induction of deletion mutations, as in the present study, the process is believed to yield successful results within a shorter period compared to traditional breeding and is safer than transgenic technology.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Bombyx / Barajamiento de ADN / Quinurenina 3-Monooxigenasa / Edición Génica Tipo de estudio: Risk_factors_studies Límite: Animals Idioma: En Revista: Biotechnol Prog Asunto de la revista: BIOTECNOLOGIA Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Bombyx / Barajamiento de ADN / Quinurenina 3-Monooxigenasa / Edición Génica Tipo de estudio: Risk_factors_studies Límite: Animals Idioma: En Revista: Biotechnol Prog Asunto de la revista: BIOTECNOLOGIA Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos