Your browser doesn't support javascript.
loading
Efficient and specific generation of knockout mice using Campylobacter jejuni CRISPR/Cas9 system.
Lee, Jae Young; Jang, Yoo Jin; Bae, Ji Hyun; Lee, Yoon Hoo; Bae, Hee Sook; Kim, Seokjoong; Park, Sin-Gi; Koo, Ok Jae; Yeom, Su Cheong.
Afiliação
  • Lee JY; Toolgen Inc, Gasan Digital-Ro, Geumcheon, 08594, Seoul, Republic of Korea.
  • Jang YJ; Graduate School of International Agricultural Technology, Designed Animal and Transplantation Research Institute, Seoul National University, 1447 Pyeongchang-Ro, Daewha, Pyeongchang, Kangwon, 25354, Republic of Korea.
  • Bae JH; Graduate School of International Agricultural Technology, Designed Animal and Transplantation Research Institute, Seoul National University, 1447 Pyeongchang-Ro, Daewha, Pyeongchang, Kangwon, 25354, Republic of Korea.
  • Lee YH; Graduate School of International Agricultural Technology, Designed Animal and Transplantation Research Institute, Seoul National University, 1447 Pyeongchang-Ro, Daewha, Pyeongchang, Kangwon, 25354, Republic of Korea.
  • Bae HS; Toolgen Inc, Gasan Digital-Ro, Geumcheon, 08594, Seoul, Republic of Korea.
  • Kim S; Toolgen Inc, Gasan Digital-Ro, Geumcheon, 08594, Seoul, Republic of Korea.
  • Park SG; TheragenEtex Bio Institute, Suwon, 16229, Republic of Korea.
  • Koo OJ; Toolgen Inc, Gasan Digital-Ro, Geumcheon, 08594, Seoul, Republic of Korea.
  • Yeom SC; Graduate School of International Agricultural Technology, Designed Animal and Transplantation Research Institute, Seoul National University, 1447 Pyeongchang-Ro, Daewha, Pyeongchang, Kangwon, 25354, Republic of Korea.
Biochem Biophys Rep ; 22: 100752, 2020 Jul.
Article em En | MEDLINE | ID: mdl-32258440
ABSTRACT
The Streptococcus pyogenes CRISPR/Cas9 (SpCas9) system is now widely utilized to generate genome engineered mice; however, some studies raised issues related to off-target mutations with this system. Herein, we utilized the Campylobacter jejuni Cas9 (CjCas9) system to generate knockout mice. We designed sgRNAs targeting mouse Tyr or Foxn1 and microinjected into zygotes along with CjCas9 mRNA. We obtained newborn mice from the microinjected embryos and confirmed that 50% (Tyr) and 38.5% (Foxn1) of the newborn mice have biallelic mutation on the intended target sequences, indicating efficient genome targeting by CjCas9. In addition, we analyzed off-target mutations in founder mutant mice by targeted deep sequencing and whole genome sequencing. Both analyses revealed no off-target mutations at potential off-target sites predicted in silico and no unexpected random mutations in analyzed founder animals. In conclusion, the CjCas9 system can be utilized to generate genome edited mice in a precise manner.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Biochem Biophys Rep Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Biochem Biophys Rep Ano de publicação: 2020 Tipo de documento: Article